HBA1 抗体 (Middle Region)
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北京 101111
Quick Overview for HBA1 抗体 (Middle Region) (ABIN952707)
抗原
See all HBA1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 107-136, Middle Region
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特异性
- This antibody recognizes Human and Mouse Hemoglobin alpha (Center).
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纯化方法
- Protein A column, followed by peptide affinity purification
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免疫原
- KLH conjugated synthetic peptide between 107~136 amino acids from the Central region of human Hemoglobin alpha Genename: HBA2, HBA1
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亚型
- Ig Fraction
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- HBA1 (Hemoglobin, alpha 1 (HBA1))
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别名
- Hemoglobin alpha
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背景
- HBA2 located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97 % of the total hemoglobin, alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3 % of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1, some nondeletion alpha thalassemias have also been reported.Synonyms: Alpha-globin, HBA1, Hemoglobin alpha chain
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分子量
- 15258 Da
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基因ID
- 3039
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NCBI登录号
- NP_000508
抗原
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