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HBa2 抗体 (AA 100-128)

This anti-HBa2 antibody is a 兔 多克隆 antibody detecting HBa2 in WB, FACS 和 IHC (p). Suitable for 人 和 小鼠.
产品编号 ABIN5533268
发货至: 中国

Quick Overview for HBa2 抗体 (AA 100-128) (ABIN5533268)

抗原

See all HBa2 抗体
HBa2 (Hemoglobin, alpha 2 (HBa2))

适用

  • 7
  • 2
  • 1
人, 小鼠

宿主

  • 8

克隆类型

  • 8
多克隆

标记

  • 4
  • 1
  • 1
  • 1
  • 1
This HBa2 antibody is un-conjugated

应用范围

  • 8
  • 5
  • 5
  • 5
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 5
    • 5
    • 5
    • 1
    • 1
    AA 100-128

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This HBA2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 100-128 amino acids from the Central region of human HBA2.

    亚型

    Ig Fraction
  • 应用备注

    For FACS starting dilution is: 1:25

    For WB starting dilution is: 1:1000

    For IHC-P starting dilution is: 1:50~100

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 mg/mL

    缓冲液

    Supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    储存方法

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 抗原

    HBa2 (Hemoglobin, alpha 2 (HBa2))

    别名

    HBA2

    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.

    分子量

    15 kDa

    基因ID

    3039, 3040

    UniProt

    P69905
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