PPT-Figure Figure. Direct fluorescent-antibody (DFA) staining of Bacillus anthracis
Author : ruby | Published Date : 2023-07-08
De BK Bragg SL Sanden GN Wilson KE Diem LA Marston CK et al TwoComponent Direct FluorescentAntibody Assay for Rapid Identification of Bacillus anthracis Emerg Infect
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Figure Figure. Direct fluorescent-antibody (DFA) staining of Bacillus anthracis: Transcript
De BK Bragg SL Sanden GN Wilson KE Diem LA Marston CK et al TwoComponent Direct FluorescentAntibody Assay for Rapid Identification of Bacillus anthracis Emerg Infect Dis 200281010601065 httpsdoiorg103201eid0810020392. . sp. Basmah. . almaarik. #Lab . 9. Bacillus culture. Spore forming facultative anaerobic bacteria.. Grow every where cause it produce spores.. Grow in wide rage 12-45 ºC. Spore formation is best seen in 25 – 30 ºC. . Bacillus anthracis. Introduction. . Anthrax is caused by the large Gram-positive, rod-shaped, spore-forming bacterium, . Bacillus . anthracis. .. Anthrax can be found naturally in the soil.. Bacillus anthracis and its activity in Anthrax Lance Morrison General anthrax info Identified in 1800s Mostly effected livestock (transmit to humans) Showed to be related to B. anthracis in 1876 (Robert Koch) fpkm. ). PD-L1 (. fpkm. ). CD8 (. fpkm. ). Iba1 (. fpkm. ). p. < 0.001. p. < 0.001. p. < 0.001. p. < 0.001. GM-CSF. GM-CSF. GM-CSF. GM-CSF. Supplemental Figure 1. Gene expression analysis in breast cancer cases from TCGA database. Gene expression levels of CD8, Iba1, PD-L1, and PD-L2 in breast cancer were compared between the cases with and without GM-CSF expression. The Mann-Whitney . Jernigan JA, Stephens DS, Ashford DA, Omenaca C, Topiel MS, Galbraith M, et al. Bioterrorism-Related Inhalational Anthrax: The First 10 Cases Reported in the United States. Emerg Infect Dis. 2001;7(6):933-944. https://doi.org/10.3201/eid0706.010604. Harvala H, McIntyre CL, Imai N, Clasper L, Djoko CF, LeBreton M, et al. High Seroprevalence of Enterovirus Infections in Apes and Old World Monkeys. Emerg Infect Dis. 2012;18(2):283-286. https://doi.org/10.3201/eid1802.111363. Jackson ML, Rose CE, Cohn A, Coronado F, Clark TA, Wenger JD, et al. Modeling Insights into Haemophilus influenzae Type b Disease, Transmission, and Vaccine Programs. Emerg Infect Dis. 2012;18(1):13-20. https://doi.org/10.3201/eid1801.110336. Sohn YM. Japanese Encephalitis Immunization in South Korea: Past, Present, and Future. Emerg Infect Dis. 2000;6(1):17-24. https://doi.org/10.3201/eid0601.000103. Pantoja CR, Navarro SA, Naranjo J, Lightner DV, Gerba CP. Nonsusceptibility of Primate Cells to Taura Syndrome Virus. Emerg Infect Dis. 2004;10(12):2106-2112. https://doi.org/10.3201/eid1012.040419. Yang J, Ramanathan MP, Muthumani K, Choo AY, Jin S, Yu Q, et al. Induction of Inflammation by West Nile virus Capsid through the Caspase-9 Apoptotic Pathway. Emerg Infect Dis. 2002;8(12):1379-1384. https://doi.org/10.3201/eid0812.020224. Pasick J, Berhane Y, Embury-Hyatt C, Copps J, Kehler H, Handel K, et al. Susceptibility of Canada Geese (Branta canadensis) to Highly Pathogenic Avian Influenza Virus (H5N1). Emerg Infect Dis. 2007;13(12):1821-1827. https://doi.org/10.3201/eid1312.070502. Perkins BA, Popovic T, Yeskey K. Public Health in the Time of Bioterrorism. Emerg Infect Dis. 2002;8(10):1015-1018. https://doi.org/10.3201/eid0810.020444. Poccia F, Gioia C, Montesano C, Martini F, Horejsh D, Castilletti C, et al. Flow Cytometry and T-Cell Response Monitoring after Smallpox Vaccination. Emerg Infect Dis. 2003;9(11):1468-1470. https://doi.org/10.3201/eid0911.030349. Hussain AI, Shanmugam V, Switzer WM, Tsang SX, Fadly A, Thea D, et al. Lack of Evidence of Endogenous Avian Leukosis Virus and Endogenous Avian Retrovirus Transmission to Measles Mumps Rubella Vaccine Recipients. Emerg Infect Dis. 2001;7(1):66-72. https://doi.org/10.3201/eid0701.700066.
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