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.
To calculate the molar solubility of CaCO₃ (calcium carbonate) using its solubility product constant (Ksp), you start with the dissolution equation: CaCO₃ (s) ⇌ Ca²⁺ (aq) + CO₃²⁻ (aq). The Ksp expression is Ksp = [Ca²⁺][CO₃²⁻]. If you let the molar solubility be "s," then at equilibrium, [Ca²⁺] = s and [CO₃²⁻] = s, giving Ksp = s². Setting this equal to 4.5 x 10⁻⁹, you solve for s: s² = 4.5 x 10⁻⁹, which gives s = √(4.5 x 10⁻⁹) ≈ 6.7 x 10⁻⁵ M.
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.