Hemoglobin A2
Hemoglobin A2 structure
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Common Name | Hemoglobin A2 | ||
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| CAS Number | 9034-53-1 | Molecular Weight | N/A | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | N/A | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
| Name | hemoglobin-a2 |
|---|---|
| Synonym | More Synonyms |
| Appearance of Characters | lyophilized powder |
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| Storage condition | -20°C |
| Hazard Codes | B |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
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Prevalence of thalassaemia, iron-deficiency anaemia and glucose-6-phosphate dehydrogenase deficiency among Arab migrating nomad children, southern Islamic Republic of Iran.
East. Mediterr. Health J. 20(11) , 726-31, (2014) This study investigated the prevalence of iron-deficiency anaemia, glucose-6-phosphate dehydrogenase (G6PD) deficiency and β-thalassaemia trait among Arab migrating nomad children in southern Islamic ... |
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Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.
Clin. Chim. Acta 413(19-20) , 1705-7, (2012) An increased HbA2 level is the hallmark for identification of β thalassemia carriers. However, in some carriers the level of HbA2 is not typically elevated creating difficulties in making a diagnosis.... |
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α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.
Hemoglobin 36(5) , 511-5, (2012) We describe two frameshift mutations associated with an α-thalassemia (α-thal) phenotype, identified in three unrelated individuals investigated for persistent microcytosis. The first mutation, HBA2:c... |
| EINECS 232-897-1 |