HBA1 抗体
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北京 101111
Quick Overview for HBA1 抗体 (ABIN7881006)
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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原理
- Hemoglobin alpha Antibody / HBA1/2
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序列
- AVHASLDKFL ASVSTVLTSK YR
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纯化方法
- Antigen affinity purified
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免疫原
- Amino acids AVHASLDKFLASVSTVLTSKYR from the human protein were used as the immunogen for the Hemoglobin alpha antibody.
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亚型
- IgG
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anti-Hemoglobin, alpha 1 (HBA1) (AA 1-142) antibody
HBA1 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) antibodyHBA1 适用: 人 WB, IHC, IF 宿主: 兔 Monoclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 1-142) antibodyHBA1 适用: 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 2-142) antibodyHBA1 适用: Cow WB 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 33-142) antibodyHBA1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4F9 unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 1-142) antibodyHBA1 适用: 人 WB, IHC 宿主: 小鼠 Monoclonal C5 unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 2-142) antibodyHBA1 适用: 人 WB, IHC, FACS 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 107-136), (Middle Region) antibodyHBA1 适用: 人, 小鼠 WB, FACS, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 33-142) antibodyHBA1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Hemoglobin, alpha 1 (HBA1) (AA 2-142) antibodyHBA1 适用: 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the Hemoglobin alpha antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the Hemoglobin alpha antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- HBA1 (Hemoglobin, alpha 1 (HBA1))
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别名
- Hemoglobin alpha
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背景
- 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.
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UniProt
- P69905
抗原
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