Hemoglobin produced in association with the sickle cell trait; the beta-globin molecules of hemoglobin S are defective.
sickle trait hemoglobin
hemoglobin is what give the red blood cells it,s clour
glutamic acid is replaced by valine in the beta chain
4 months
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 SS disease (Hb SS)
i think it`s hemoglobin
H. Lehmann has written: 'Human haemoglobin variants and their characteristics' -- subject(s): Hemoglobin, Tables 'Man's haemoglobins' -- subject(s): Hemoglobin, Hemoglobinopathy
Do hemoglogin electrophoresis
A hemoglobin is a red protein responsible for transporting oxygen in the blood of vertebrates. Its molecule comprises four subunits, each containing an iron atom bound to a heme group. TO answer your question. THe answer is a big, fat "NO".
Hemoglobin S. This the predominant hemoglobin in people with sickle cell disease. The alpha chain is normal. The disease-producing mutation exists in the beta chain, giving the molecule the structure, a2bS2. People who have one sickle mutant gene and one normal beta gene have sickle cell trait which is benign.
Robert M. Winslow has written: 'Advances in Blood Substitutes' 'Hemoglobin-based red cell substitutes' -- subject(s): Blood Substitutes, Hemoglobin