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HBA1 抗体 (AA 30-110)

This 兔 多克隆 anti-HBA1 antibody specifically detects HBA1 in WB 和 ELISA. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7228850
发货至: 中国
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Quick Overview for HBA1 抗体 (AA 30-110) (ABIN7228850)

抗原

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

适用

  • 46
  • 28
  • 13
  • 2
  • 2
人, 小鼠, 大鼠

宿主

  • 50
  • 7

克隆类型

  • 39
  • 18
多克隆

标记

  • 29
  • 6
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This HBA1 antibody is un-conjugated

应用范围

  • 39
  • 25
  • 17
  • 17
  • 12
  • 8
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 14
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 30-110

    原理

    HBA Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of HBA protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human HBA protein at AA range: 30-110

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    HBA

    背景

    Rabbit Anti-HBA Polyclonal Antibody,Alpha-globin, Hemoglobin alpha chain,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.,HBA

    分子量

    observerd band 15kDa

    基因ID

    3039

    UniProt

    P69905
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