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HBA1 抗体

This anti-HBA1 antibody is a 兔 单克隆 antibody detecting HBA1 in IHC (p). Suitable for 人.
产品编号 ABIN7091200
发货至: 中国

Quick Overview for HBA1 抗体 (ABIN7091200)

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

  • 44
  • 9
单克隆

标记

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

应用范围

  • 39
  • 24
  • 17
  • 12
  • 10
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

H8D6
  • 预测反应

    Human,Mouse,Rat

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human HBA1

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

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

    储存条件

    4 °C,-20 °C

    储存方法

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    HBA1

    背景

    Synonyms: Alpha 1 globin, Alpha globin, Alpha one globin, Alpha-globin, HBA_HUMAN, HBA2, Hemoglobin alpha 1, Hemoglobin alpha 1 chain, Hemoglobin alpha 1 globin chain, Hemoglobin alpha 2, Hemoglobin alpha chain, Hemoglobin subunit alpha, MGC126895, MGC12689.

    Background: he 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]

    基因ID

    3039

    UniProt

    P69905
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