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HBA1 抗体 (AA 30-110)

This 兔 多克隆 antibody specifically detects HBA1 in WB 和 ELISA. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN8121923
发货至: 中国
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Quick Overview for HBA1 抗体 (AA 30-110) (ABIN8121923)

抗原

See all HBA1 抗体
HBA1 (Hemoglobin, alpha 1 (HBA1))

适用

  • 69
  • 31
  • 15
  • 2
  • 2
人, 小鼠, 大鼠

宿主

  • 71
  • 9
兔

克隆类型

  • 53
  • 27
多克隆

标记

  • 42
  • 7
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HBA1 antibody is un-conjugated

应用范围

  • 53
  • 43
  • 21
  • 18
  • 15
  • 8
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 25
    • 9
    • 8
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 30-110

    原理

    HBA Antibody

    特异性

    HBA Polyclonal Antibody detects endogenous levels of protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from human protein . at AA range: 30-110

    亚型

    IgG
  • 应用备注

    WB 1:500-2000 ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    HBA

    背景

    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],

    Gene Name: HBA1; HBA2

    Protein Name: Hemoglobin subunit alpha (Alpha-globin) (Hemoglobin alpha chain)

    基因ID

    3039

    UniProt

    P69905
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