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Please refer disclaimer Overleaf.Motility Test MediumM260Motility Test Please refer disclaimer Overleaf.Motility Test MediumM260Motility Test

Please refer disclaimer Overleaf.Motility Test MediumM260Motility Test - PDF document

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Please refer disclaimer Overleaf.Motility Test MediumM260Motility Test - PPT Presentation

Ingredients Gms Litre Tryptose 10000 Sodium chloride 5000 Agar 5000 Final pH at 25 ID: 125375

Ingredients Gms Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final

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10.000 Sodium chloride 5.000 Agar 5.000 Cultural Response Escherichia coli ATCC 50-100 luxuriant positive, HiMedia Laboratories Technical Data from stablinecausing Enterobacter aerogenes 50-100 luxuriant positive, Klebsiella pneumoniae 50-100 luxuriant negative, Salmonella Enteritidis ATCC 50-100 luxuriant positive, Staphylococcus aureus 50-100 luxuriant negative, 1.Koneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C., Winn W. C. Jr., (Eds.), 1992, Colour Atlas and Textbook4.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, WilliamsUser must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not Please refer disclaimer Overleaf.M260 Motility Test Medium Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Organism Inoculum Growth Motility Cultural Response Escherichia coli ATCC 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Motility Test Medium Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Organism Inoculum Growth Motility Cultural Response Escherichia coli ATCC 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Motility Test Medium Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Organism Inoculum Growth Motility Cultural Response Escherichia coli ATCC 50-100 luxuriant positive, HiMedia Laboratories Technical Data from stablinecausing Enterobacter aerogenes 50-100 luxuriant positive, Klebsiella pneumoniae 50-100 luxuriant negative, Salmonella Enteritidis ATCC 50-100 luxuriant positive, Staphylococcus aureus 50-100 luxuriant negative, Reference 1.Koneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C., Winn W. C. Jr., (Eds.), 1992, Colour Atlas and Textbook4.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, WilliamsUser must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not Please refer disclaimer Overleaf.M260 Motility Test Medium Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Cultural ResponseCultural characteristics observed after an incubation at 35 - 37°C for 18 - 48 hours. Organism Inoculum Growth Motility Escherichia coli ATCC 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Cultural Response Organism Inoculum Growth Motility Escherichia coli ATCC 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) Suspend 20 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes and sterilizeBacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Cultural Response Organism Inoculum Growth Motility Escherichia coli ATCC 50-100 luxuriant positive, User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not HiMedia Laboratories Technical Data from stablinecausing Enterobacter aerogenes 50-100 luxuriant positive, Klebsiella pneumoniae 50-100 luxuriant negative, Salmonella Enteritidis ATCC 50-100 luxuriant positive, Staphylococcus aureus 50-100 luxuriant negative, Reference 1.Koneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C., Winn W. C. Jr., (Eds.), 1992, Colour Atlas and Textbook4.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Cultural ResponseCultural characteristics observed after an incubation at 35 - 37°C for 18 - 48 hours. Organism Inoculum Growth Motility Escherichia coli ATCC 50-100 luxuriant positive, User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should notKoneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C., Winn W. C. Jr., (Eds.), 1992, Colour Atlas and TextbookMacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams HiMedia Laboratories Technical Data from stablinecausing Enterobacter aerogenes 50-100 luxuriant positive, Klebsiella pneumoniae 50-100 luxuriant negative, Salmonella Enteritidis ATCC 50-100 luxuriant positive, Staphylococcus aureus 50-100 luxuriant negative, HiMedia Laboratories Technical Data from stablinecausingturbidity Enterobacter aerogenesATCC 13048 50-100 luxuriant positive,from stablinecausingturbidity Klebsiella pneumoniaeATCC 13883 50-100 luxuriant negative,the stabline,surroundingmediumremains clear Salmonella Enteritidis ATCC 50-100 luxuriant positive,from stablinecausingturbidity Staphylococcus aureusATCC 25923 50-100 luxuriant negative,the stabline,surroundingmediumremains clear Quality ControlAppearanceCream to yellow homogeneous free flowing powderGellingSemisolid, comparable with 0.5% Agar gel.Colour and Clarity of prepared mediumLight yellow coloured clear to slightly opalescent gel forms in tubes as buttsReactionReaction of 2.0% w/v aqueous solution at 25°C. pH : 7.2±0.2pH7.00-7.40Cultural ResponseCultural characteristics observed after an incubation at 35 - 37°C for 18 - 48 hours. Organism Inoculum(CFU) Growth Motility Escherichia coli ATCC25922 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Koneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C., Winn W. C. Jr., (Eds.), 1992, Colour Atlas and Textbook4.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams HiMedia Laboratories Technical Data from stablinecausing Enterobacter aerogenes 50-100 luxuriant positive, Klebsiella pneumoniae 50-100 luxuriant negative, Salmonella Enteritidis ATCC 50-100 luxuriant positive, Staphylococcus aureus 50-100 luxuriant negative, Quality ControlAppearanceCream to yellow homogeneous free flowing powderGellingSemisolid, comparable with 0.5% Agar gel.Colour and Clarity of prepared mediumLight yellow coloured clear to slightly opalescent gel forms in tubes as buttsReactionReaction of 2.0% w/v aqueous solution at 25°C. pH : 7.2±0.2pH7.00-7.40Cultural ResponseCultural characteristics observed after an incubation at 35 - 37°C for 18 - 48 hours. Organism Inoculum Growth Motility Escherichia coli ATCC 50-100 luxuriant positive, Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet ) Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tryptose 10.000 Sodium chloride 5.000 Agar 5.000 Final pH ( at 25°C) 7.2±0.2**Formula adjusted, standardized to suit performance parameters otrieied . distilled water. Heat to boiling to dissolve the medium completely. Dispense in tubes Bacterial motility can be observed directly on microscopic slide or it can be visualized on motility media having agarconcentration of 0.4% or less (1). Use of such semisolid media to observe or detect motility was reported by Tittsler andSandholzer (2). Motility Test Medium is a modification of their formulation. Motility can be visualized as a diffused zone ofgrowth flaring out from the line of inoculation (1). Hanging-drop technique in motility tests has practical difficulties, whichis efficiently eliminated by use of culture-based methods using semi-solid media, as in semisolid media; the results obtainedTryptose serve as a source of essential growth nutrients required for bacterial metabolism. Sodium chloride maintains theBacterial motility can be observed directly by examination of the tubes following incubation. Inoculation is done by stabbingthrough the centre of the medium. Incubate at appropriate temperature for 18-40 hours. Non-motile organisms grow only alongthe line of inoculation whereas motile organisms grow away from the line of inoculation or may show growth even throughoutthe medium. All weak or equivocal motility results should be confirmed by flagellum stain or by direct wet microscopy (hanging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet ) User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet ) lax ae reeerred in indiuidtak HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniaeATCC 13883 Salmonella Enteritidis ATCC13076 Staphylococcus aureusATCC 25923 Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum(CFU) Growth Motility Escherichia coli ATCC25922 Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet ) lax ae reeerred in indiuidtak HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniaeATCC 13883 Salmonella Enteritidis ATCC13076 Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum(CFU) Growth Motility Escherichia coli ATCC25922 Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet ) Qead tge lax ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet )4,5*. Qead tge lax ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Fos tanplet gollow appsopsiate tediniruet gos ianeling pes ettablitiee guieelinet )4,5*. Qead tge lax ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge lax ae reeerred in indiuidtak HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge ae reeerred in indiuidtak Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge lax ae reeerred in indiuidtakgrnvtg ne Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge lax ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge lax ae reeerred in indiuidtak User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Qead tge lax ae reeerred in 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not1.Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane Textbook 4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Witi inodulating neeele, ttab dentse og neeiun to appsoxinately one.ialg og eepti.)4* Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane 4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane 4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane 4.MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: HiMedia Laboratories Technical Data Enterobacter aerogenes Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving agasdondentsation og 1.4% os lett )1*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles aneTaneiolzes )3*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone oggsowti glasing out gson tie line og inodulation )1*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, wiidiit eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt obtaineeTsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint tieCadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy )ianging Witi inodulating neeele, ttab dentse og neeiun to appsoxinately one.ialg og eepti.)4* Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Principle And Interpretation Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving dondentsation og 1.4% os lett )*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles Taneiolzes )*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone gsowti glasing out gson tie line og inodulation )*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, it eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt Tsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint Cadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy Witi inodulating neeele, ttab dentse og neeiun to appsoxinately one.ialg og eepti.)4* Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) HiMedia Laboratories Technical Data Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. HiMedia Laboratories Technical Data Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC Please refer disclaimer Overleaf. HiMedia Laboratories Technical Data Klebsiella pneumoniae Salmonella Enteritidis ATCC Staphylococcus aureus Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC 25922 Please refer disclaimer Overleaf. HiMedia Laboratories Technical Data Klebsiella pneumoniaeATCC 13883 Salmonella Enteritidis ATCC 13076 Staphylococcus aureusATCC 25923 Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC 25922 Please refer disclaimer Overleaf. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Principle And Interpretation Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving dondentsation og 1.4% os lett )*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles Taneiolzes )*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone gsowti glasing out gson tie line og inodulation )*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, it eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt Tsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint Cadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: .EAnato R. F., ane Tongoiseee K. M., 1991, K. Clin. Midsobiol., 14 )4*, 447.449. Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Principle And Interpretation Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving dondentsation og 1.4% os lett )*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles Taneiolzes )*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone gsowti glasing out gson tie line og inodulation )*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, it eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt Tsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint Cadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Principle And Interpretation Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving dondentsation og 1.4% os lett )*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles Taneiolzes )*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone gsowti glasing out gson tie line og inodulation )*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, it eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt Tsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint Cadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) Please refer disclaimer Overleaf.M260 Ingredients Gms / Litre Tutpene 31 gsant in 1111 nl pusigiee 0 eittillee wates. Heat to boiling to eittolve tie neeiun donpletely. Eitpente in tubet ttesilize by autodlaving at 15 lbt psettuse )131°C* gos 15 ninutet. Allow tubee neeiun to dool to 45.51°C in an upsigit Principle And Interpretation Cadtesial notility dan be obtesvee eisedtly on nidsotdopid tliee os it dan be vitualizee on notility neeia iaving dondentsation og 1.4% os lett )*. Ute og tudi tenitolie neeia to obtesve os eetedt notility wat sepostee by Titttles Taneiolzes )*. Motility Tett Meeiun it a noeigidation og tieis gosnulation. Motility dan be vitualizee at a eiggutee zone gsowti glasing out gson tie line og inodulation )*. Hanging.esop tedinirue in notility tettt iat psadtidal eiggidultiet, it eggidiently elininatee by ute og dultuse.batee netioet uting teni.tolie neeia, at in tenitolie neeia; tie setultt Tsyptote tesve at a tousde og ettential gsowti nutsientt seruisee gos badtesial netabolitn. Toeiun dilosiee naintaint Cadtesial notility dan be obtesvee eisedtly by exanination og tie tubet gollowing indubation. Inodulation it eone by ttabbingtisougi tie dentse og tie neeiun. Indubate at appsopsiate tenpesatuse gos 19.41 ioust. Non.notile osganitnt gsow only alongtie line og inodulation wieseat notile osganitnt gsow away gson tie line og inodulation os nay tiow gsowti even tisougiouttie neeiun. All weak os eruivodal notility setultt tioule be dongisnee by glagellun ttain os by eisedt wet nidsotdopy Qead tge lax ae reeerred in indiuidtak 1.Akk veaj nr eptiunbak lntikitx restkts sgntkd ae bnneirled ax ekagekktl stain nr ax direbt vet librnsbnox (ganging drno) HiMedia Laboratories Technical Data Klebsiella pneumoniaeATCC 13883 Salmonella ATCC13076 Staphylococcus aureusATCC 25923 Quality ControlAppearanceGellingColour and Clarity of prepared mediumReactionpHCultural Response Organism Inoculum Growth Motility Escherichia coli ATCC 25922 Please refer disclaimer Overleaf. Utes nutt entuse tuitability og tie psoeudt)t* in tieis applidation psios to ute. Psoeudtt dongosn tolely to tie ingosnation dontainee intiit ane oties selatee HiMeeia™ publidationt. Tie ingosnation dontainee in tiit publidation it batee on ous seteasdi ane eevelopnentwosk ane it to tie bett og ous knowleege tsue ane addusate. HiMeeia™ Labosatosiet Pvt Lte setesvet tie sigit to nake dianget totpedigidationt ane ingosnation selatee to tie psoeudtt at any tine. Psoeudtt ase not inteneee gos iunan os aninal os tiesapeutid ute butgos labosatosy,eiagnottid, seteasdi os gusties nanugadtusing ute only, unlett otieswite tpedigiee. Ttatenentt dontainee iesein tioule not Konenan E. W., Allen T. E., Kanea W. M., Tdisedkenbesges P. C., Winn W. C. Ks., )Eet.*, 1993, Colous Atlat ane MadFaeein K. F., 1995, Meeia gos Itolation.Cultivation.Ieentigidation.Maintenande og Meeidal Cadtesia, Vol. 1, Williant HiMedia Laboratories Technical Data tge orndtbt lax bnntainer tiggtkx Tse aeenre ewoirx date nn tge kaaek. Utes nutt entuse tage eitpotal by autodlaving ane0os indinesation og utee os unutable psepasationt og tiit psoeudt. Follow ettablitiee labosatosy psodeeuset in eitpoting og ingedtiout natesialt ane natesial tiat donet into dontadt witi tanple nutt HiMeeia Labosatosiet Pvt. Lte. Reg.oggide : 34, Vaeiani Ine.Ett., LCT Masg, Munbai.411197, Cuttones dase No.: 133.7117 oggide : A.517,Twattik Eitia Cutinett Pask,Via Vaeiani Ine. Ett., LCT Masg, Munbai.411197, Ineia. Cuttones dase No.: 133.7147 1919 Enail: .EAnato R. F., ane Tongoiseee K. M., 1991, K. Clin. Midsobiol., 14 )4*, 447.449.