glutamic acid is replaced by valine in the beta chain
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Hemoglobin produced in association with the sickle cell trait; the beta-globin molecules of hemoglobin S are defective.
"A molecule consisting of 4 subunits, at least 1 of which differs from the others." A hemoglobin has 4 subunits
The difference in electrophoretic pattern between normal hemoglobin A and hemoglobin S is due to a single amino acid substitution. In hemoglobin S, a glutamic acid is replaced by a valine at position 6 of the beta-globin chain. This change causes hemoglobin S to have a different charge, leading to its characteristic migration pattern on electrophoresis.
hemoglobin is what give the red blood cells it,s clour
Sickle cell hemoglobin differs from normal hemoglobin due to a mutation in the gene that codes for the hemoglobin protein. This mutation leads to the production of an abnormal hemoglobin variant (HbS) that causes red blood cells to become sickle-shaped, leading to various complications such as blockages in blood vessels and reduced oxygen delivery to tissues.
Hemoglobin S refers to the hemoglobin that forms in patients with sickle cell anemia. Hemoglobin solubility is a test that can be performed in order to determine if the patient has sickle cell anemia.
4 months
hemoglobin
what is hemoglobin?
No, hemoglobin is a protein.
Hypochromia (as in hypochromic anemia) is the medical term meaning deficiency in hemoglobin.