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.
Hemoglobin produced in association with the sickle cell trait; the beta-globin molecules of hemoglobin S are defective.
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.
s the equator and the diameter the same thing?
hemoglobin is what give the red blood cells it,s clour
glutamic acid is replaced by valine in the beta chain
4 months
no
It was like.... the same thing.
The same thing as men. Lived.
H. Lehmann has written: 'Human haemoglobin variants and their characteristics' -- subject(s): Hemoglobin, Tables 'Man's haemoglobins' -- subject(s): Hemoglobin, Hemoglobinopathy
Hemoglobin electrophoresis uses stains such as Coomassie blue or Ponceau S to visualize the globin chains of the hemoglobin molecule. These stains help separate and identify different types of hemoglobin based on the migration pattern of the globin chains.
Sarawadee Junsophonsri has written: 'Solubility of biocides in pure and modified supercritical carbon dioxide' -- subject(s): Poisons, Solubility