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HBA1 抗体 (AA 1-100)

This anti-HBA1 antibody is a 兔 多克隆 antibody detecting HBA1 in WB. Suitable for 人.
产品编号 ABIN7267609
发货至: 中国

Quick Overview for HBA1 抗体 (AA 1-100) (ABIN7267609)

抗原

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

适用

  • 39
  • 20
  • 4
  • 3
  • 2

宿主

  • 45
  • 8

克隆类型

  • 43
  • 10
多克隆

标记

  • 32
  • 7
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HBA1 antibody is un-conjugated

应用范围

  • 38
  • 24
  • 17
  • 12
  • 10
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 15
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-100

    原理

    Hemoglobin subunit alpha (HBA1) Rabbit pAb

    序列

    MVLSPADKTN VKAAWGKVGA HAGEYGAEAL ERMFLSFPTT KTYFPHFDLS HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK

    交叉反应

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    A synthetic peptide corresponding to a sequence within amino acids 1-100 of human Hemoglobin subunit alpha (Hemoglobin subunit alpha (HBA1)) (NP_000549.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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. Avoid freeze / thaw cycles.
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    HBA1

    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.,HBA1,HBA-T3,HBH,HBA1

    分子量

    15kDa

    基因ID

    3039

    UniProt

    P69905
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