血红蛋白A2,经亚铁稳定人

更新时间：2024-01-10 07:16:14

血红蛋白A2,经亚铁稳定人结构式	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

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 ...

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....

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