血红蛋白A2,经亚铁稳定 人结构式
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常用名 | 血红蛋白A2,经亚铁稳定 人 | 英文名 | Hemoglobin A2 |
|---|---|---|---|---|
| CAS号 | 9034-53-1 | 分子量 | N/A | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | N/A | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A |
| 中文名 | 血红蛋白A2 |
|---|---|
| 英文名 | hemoglobin-a2 |
| 英文别名 | 更多 |
| 外观性状 | lyophilized powder |
|---|---|
| 储存条件 | -20°C |
| 危害码 (欧洲) | B |
|---|---|
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 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 |
