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.
hemoglobin is what give the red blood cells it,s clour
glutamic acid is replaced by valine in the beta chain
4 months
A substance which can dissolve in a solvent is said to be soluble in that solvent
Oxygen is carried by hemoglobin in red blood cells because it is not very soluble in blood plasma. Hemoglobin binds to oxygen in the lungs and releases it to tissues where it is needed. This allows for efficient transport of oxygen throughout the body.
H. Lehmann has written: 'Human haemoglobin variants and their characteristics' -- subject(s): Hemoglobin, Tables 'Man's haemoglobins' -- subject(s): Hemoglobin, Hemoglobinopathy
AL+S is "soluble"
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.
Oxygen is less soluble in water at higher temperatures. While the primary transport mechanism for oxygen in the blood is hemoglobin and not water, it is still true that the oxygen has to pass from the hemoglobin into the various fluids of the body in order to be accessible to the cells for metabolism.