Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (AA 10-60) 抗体
Quick Overview for Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (AA 10-60) 抗体 (ABIN1387969)
抗原
See all Hemoglobin Alpha 1 + 2 (HBA1,HBA2) 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 10-60
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交叉反应
- 人, 小鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human Hemoglobin alpha
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亚型
- IgG
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anti-Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (Internal Region) antibody
HBA1,HBA2 适用: 人 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (AA 100-128) antibodyHBA1,HBA2 适用: 人, 小鼠 WB, IHC, IHC (p), FACS 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin Alpha 1 + 2 (HBA1,HBA2) antibody (Biotin)HBA1,HBA2 适用: 小鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal Biotin
anti-Hemoglobin Alpha 1 + 2 (HBA1,HBA2) antibody (FITC)HBA1,HBA2 适用: 小鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal FITC
anti-Hemoglobin Alpha 1 + 2 (HBA1,HBA2) antibody (HRP)HBA1,HBA2 适用: 小鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal HRP
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应用备注
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IHC-P 1:200-400
IF(IHC-P) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- Hemoglobin Alpha 1 + 2 (HBA1,HBA2)
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别名
- HBA1+HBA2
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背景
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Synonyms: HBH, HBA-T3, Hemoglobin subunit alpha, Alpha-globin, Hemoglobin alpha chain, HBA1
Background: The human alpha globin gene cluster 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. [provided by RefSeq, Jul 2008].
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基因ID
- 3039
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UniProt
- P69905
抗原
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