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%ما هو (من)٪ 1 - تعريف
VARIANT OF HEMOGLOBIN A
Hemoglobin a2; Haemoglobin a2; Haemoglobin A2; Hb A2
Hemoglobin
GROUP OF PROTEIN COMPLEXES
Haemoglobin; Oxyhemoglobin; Haemoglobin (hb); Oxyhaemoglobin; Hæmoglobin; Hämoglobin; Deoxyhemoglobin; Haemaglobin; Hemoglobins; Heamoglobin; Hemoglobine; Hemogoblin; Haemogloben; Hemogloben; Hamoglobin; Oxygen binding capacity; O2 capacity; Hemoglobin deficiency; Primary hemoglobin deficiency; Haemoglobin percentage; Heme spectra; Deoxyhaemoglobin; Haemogoblin; C3032H4816O872N780S8Fe4; Biosynthesis of hemoglobin; Deoxygenated hemoglobin
·noun The normal coloring matter of the red blood corpuscles of vertebrate animals. It is composed of hematin and globulin, and is also called haematoglobulin. In arterial blood, it is always combined with oxygen, and is then called oxyhemoglobin. It crystallizes under different forms from different animals, and when crystallized, is called haematocrystallin. ·see Blood crystal, under Blood.
Haemoglobin
GROUP OF PROTEIN COMPLEXES
Haemoglobin; Oxyhemoglobin; Haemoglobin (hb); Oxyhaemoglobin; Hæmoglobin; Hämoglobin; Deoxyhemoglobin; Haemaglobin; Hemoglobins; Heamoglobin; Hemoglobine; Hemogoblin; Haemogloben; Hemogloben; Hamoglobin; Oxygen binding capacity; O2 capacity; Hemoglobin deficiency; Primary hemoglobin deficiency; Haemoglobin percentage; Heme spectra; Deoxyhaemoglobin; Haemogoblin; C3032H4816O872N780S8Fe4; Biosynthesis of hemoglobin; Deoxygenated hemoglobin
·noun ·same·as Hemoglobin.
Oxyhemoglobin
GROUP OF PROTEIN COMPLEXES
Haemoglobin; Oxyhemoglobin; Haemoglobin (hb); Oxyhaemoglobin; Hæmoglobin; Hämoglobin; Deoxyhemoglobin; Haemaglobin; Hemoglobins; Heamoglobin; Hemoglobine; Hemogoblin; Haemogloben; Hemogloben; Hamoglobin; Oxygen binding capacity; O2 capacity; Hemoglobin deficiency; Primary hemoglobin deficiency; Haemoglobin percentage; Heme spectra; Deoxyhaemoglobin; Haemogoblin; C3032H4816O872N780S8Fe4; Biosynthesis of hemoglobin; Deoxygenated hemoglobin
·noun ·see Hemoglobin.
ويكيبيديا
Hemoglobin A2
Hemoglobin A2 (HbA2) is a normal variant of hemoglobin A that consists of two alpha and two delta chains (α2δ2) and is found at low levels in normal human blood. Hemoglobin A2 may be increased in beta thalassemia or in people who are heterozygous for the beta thalassemia gene.
HbA2 exists in small amounts in all adult humans (1.5–3.1% of all hemoglobin molecules) and is approximately normal in people with sickle-cell disease. Its biological importance is not yet known.
