PPT-Structure of Haemoglobin

THALASSEMIA It result from reduced or absent production of beta chain in globin Common Hereditary Hemoglobin disorderHHD A Beta ThalassemiaMajorIntermediaMinor trait or carrier. https://www.youtube.com/watch?v=hpaki7F4HR0. http. ://www.wisc-online.com/objects/index_tj.asp?objID=AP13304. Cells contain thousands of different proteins, each performing a specific task.. Examples: Enzymes, . Haemoglobin has ONE job – to carry oxygen around the body. It is a large protein with a quaternary structure. What are proteins?. Proteins are made up of C, H, O, N and some S and P. Transport proteins such as haemoglobin carry oxygen.. . kaur. P.G.G.C.,Sector. 11. Chandigarh. HUMAN BLOOD. HUMAN BLOOD. CONTENT . . COMPOSITION. FUNCTION OF BLOOD & LYMPH. FUNCTION OF HAEMOGLOBIN. BLOOD CLOTTING. BLOOD GROUPS & RH FACTOR. Given a set of corresponding points in two or more images, compute the camera parameters and the 3D point coordinates. Camera 1. Camera 2. Camera 3. R. 1. ,t. 1. R. 2. ,t. 2. R. 3. ,t. 3. ?. ?. ?. Slide credit: Noah . DISTRIBUTOR FACT SHEET ITEM ORDER NUMBER: 82965 Are you on ‘Team Yugi’ or ‘Team Kaiba’? Pick a side, because it’s time to Duel with more of Yugi and Kaiba’s classic card Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. globin. gene. . Sickle cell disease (SCD) is . an. . autosomal. Red Blood Cells Disorders. أ.م.د.ميسم مؤيد علوش. Objectives:. 1-Define . haemopoiesis. , main site of . haemopoiesis. and . . exteamedulary. . haemopoiesis. 2-Define the surface markers of . Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell . anaemia. Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. Here are major advantages of steel structure building including costing, safety, designs and uses. Explore here! The . sickling. phenomenon may be demonstrated in a thin. wet film of blood (sealed with a petroleum jelly/paraffin. wax mixture or with nail varnish). If . haemoglobin. S. is present, the red cells lose their smooth, round shape. . Assist. Prof. . Dr.Maysem. . Mouayad. . Alwash. . Note:. The . thalassaemias. are classified into . α. -, . β. -, . δβ. -, . γδβ. -, . δ. -, . γ. - and . εγδβ. -thalassaemias, according to the type of globin chain(s). of . haemoglobin. Ass. . Prof. . . Abeer. . Anwer. Ahmed. Normal adult blood contains three types of . haemoglobin. . Hb. . A . . Hb. . F . . Hb. . A2. Structure . Normal adult blood contains three types of. haemoglobin. . The . major component. is . haemoglobin. A with the molecular . structure . α. 2. β. 2. The minor . haemoglobins. contain . ɣ . (fetal . Dr. Mohammed Jeelani. Specific learning outcomes. List types of hemoglobin and its normal values. Describe functions and clinical significance of hemoglobin. List . the different types of WBCs. Give the normal value of each type of WBCs and its...