PPT-Haemoglobin Quiz! How many oxygen molecules can one haemoglobin molecule carry?
Author : obrien | Published Date : 2024-01-29
Oxygen dissociation curves show partial pressure of oxygen plotted against what If a species haemoglobin has a high affinity for oxygen what does this mean Why does
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Haemoglobin Quiz! How many oxygen molecules can one haemoglobin molecule carry?: Transcript
Oxygen dissociation curves show partial pressure of oxygen plotted against what If a species haemoglobin has a high affinity for oxygen what does this mean Why does CO 2 concentration alter Haemoglobins affinity for oxygen. London Speciality School of Paediatrics. August 2014. Return to Acute Paediatrics. Aims. To . reassure you that not much has . changed. To give you some gems so you can sound knowledgeable from the first ward . 10. The Variety of Life. Starter. What is the structure of haemoglobin?. Learning Objectives and Success Criteria. Describe and explain an oxygen dissociation curve. State and explain the effect of CO. 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. MD FRCEM. Emergency Medicine Consultant . Lister Hospital, Stevenage. Cyanosis. Cyanosis. What is Cyanosis?. Cyanosis. Abnormal bluish discolouration of the skin and mucous membranes.. Increased amounts of bluish-coloured haemoglobin – deoxygenated haemoglobin.. مؤيد . علو. ش. Lec. . 2. Thalassaemias. Objectives:. 1-Define thalassemia and its main types(. β. and . α. ). 2- Know the . genetic . lesions of each of . β . and . α. thalassemia. 3-Know the difference between thalassemia minor and major.. MB;BS(Ilorin), FWACP(. Paed. ). Outline. Intro /def. Normal haemoglobin structure / function. Classification of haemoglobinopathies . Structural Hb Variants. Thalassaemias. Epidemiology. Clinical features. مؤيد علوش. Introduction. THE HAEMOGLOBIN MOLECULE. Human . haemoglobin. is formed from two pairs of . globin chains . each with a . haem. . group attached.. Seven . different globin . chains are . . 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). Dr.Maysem. M. . Alwash. Sickle cell . disaese. Sickle cell disease (SCD) is an inherited chronic . haemolytic. . anaemia. . whose clinical manifestations arise from the tendency. of the . haemoglobin. Shaare. . Zedek. Medical Center. Hebrew University and Hadassah Medical School. Jerusalem, Israel. Toronto, MAB, June 21. st. 2018. SWITCH OVER DATA. Clinical trials, EAP and “real life”. Disclosures . 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 . How is a red blood cell adapted to carry out its function?. Apart from red blood cells, can you name any other examples of cells found in the blood?. How are substances transported around the body? .
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