1q}. 1. Why is cyanmethemoglobin method preferred than other methods? 2. In what circumstances is the copper sulfate method used? 3. Discuss the synthesis and breakdown of hemoglobin.?
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{1q}.
1. Why is cyanmethemoglobin method preferred than other methods?
2. In what circumstances is the copper sulfate method used?
3. Discuss the synthesis and breakdown of hemoglobin.?
Step by step
Solved in 4 steps
- Pairs). 1. Why is cyanmethemoglobin method preferred than other methods? 2. In what circumstances is the copper sulfate method used? 3. Discuss the synthesis and breakdown of hemoglobin.?1. Why is cyanmethemoglobin method preferred than other methods? 2. In what circumstances is the copper sulfate method used? 3. Discuss the synthesis and breakdown of hemoglobin.1 a) Explain the fate of hemoglobin. b) Describe 3 characteristics feature of iron deficiency anaemia.
- 1. a) True or False - A mutation in the beta globin gene that causes conversion of His146 to Glutamate would decrease Hemoglobin’s O2 binding affinity. b) True or False - A mutation in the beta globin gene that causes conversion of His146 to Glutamate would eliminate Hemoglobin’s positive cooperativity.What is BCL11A and how is it related to hemoglobin?The group of disorders associated with single gene mutations affecting amino acid sequences in the alpha and beta globin genes are called Question 10 options: A) thalassemias B) hemoglobinopathies C) hemolytic anemias D) megaloblastic anemias
- 54. The hyperviscosity syndrome associated with Waldenström macroglobulinemia is caused by which of the following? A) Aggregation of blast cells B) Erythrocytosis C) Increased serum concentration of calcium D) Increased serum concentration of IgM E) Rouleaux formation27) All of the following laboratory values are consistent with an intravascular hemolytic anemia EXCEPT() A) increased haptoglobin B) Increased lactate dehydrogenase(LDH) C) Increased reticulocyte count D) Increased unconjugated bilirubin E) Increased urine hemosiderin2. 3. 4 6. In this image, the bacteria in circles 1 and 4 is demonstrating: presence of catalase • presence of coagulase O absence of catalase O absence of coagulase presence of hydrogen peroxide absence of hydrogen peroxide presence of antibodies absence of antibodies Icst
- Relative to the position of hemoglobin A on your gel, where would you expect to find a mutant hemoglobin in which the b-chain glutamic acid residue was replaced by lysine? Sample Wall Number: 1. Normal Hemoglobin- Homoglobin AA 2. Sickle Trait Hemoglobin- Hemoglobin AS 3. Sickle Cell Hemoglobin- Hemoglobin SS 4. The unkniwn hemoglobin sample (showing the mutant sickle cell anemia trait)Caffeine is used in bilirubin assays to: 1) Stop the diazo reaction 2) Accelerate indirect bilirubin reaction 3) Accelerate direct bilirubin reaction 4) Precipitate proteins 5) Reduce sodium nitrite no references, just homework1. Briefly describe the affect of the glutamic acid to valine mutation on the Hemoglobin protein as it relates to Sickle Cell Anemia. 2. Is your prediction (from question 3 in Part I) consistent with the description of the cause of the sickle-cell anemia disease (from the BME3D computer tutorial)? Explain.
