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HBA1 抗体 (Middle Region)

This anti-HBA1 antibody is a 兔 多克隆 antibody detecting HBA1 in WB, IHC (p), FACS 和 EIA. Suitable for 人 和 小鼠.
产品编号 ABIN952707
发货至: 中国

Quick Overview for HBA1 抗体 (Middle Region) (ABIN952707)

抗原

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

适用

  • 39
  • 19
  • 4
  • 3
  • 2
人, 小鼠

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
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 15
    • 14
    • 2
    • 1
    • 1
    • 1
    AA 107-136, Middle Region

    特异性

    This antibody recognizes Human and Mouse Hemoglobin alpha (Center).

    纯化方法

    Protein A column, followed by peptide affinity purification

    免疫原

    KLH conjugated synthetic peptide between 107~136 amino acids from the Central region of human Hemoglobin alpha Genename: HBA2, HBA1

    亚型

    Ig Fraction
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.25 mg/mL

    缓冲液

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    Hemoglobin alpha

    背景

    HBA2 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.Synonyms: Alpha-globin, HBA1, Hemoglobin alpha chain

    分子量

    15258 Da

    基因ID

    3039

    NCBI登录号

    NP_000508
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