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T-Box 5 抗体

This anti-T-Box 5 antibody is a 兔 多克隆 antibody detecting T-Box 5 in WB, ELISA 和 IHC. Suitable for 人 和 犬.
产品编号 ABIN2460713
发货至: 中国

Quick Overview for T-Box 5 抗体 (ABIN2460713)

抗原

See all T-Box 5 (TBX5) 抗体
T-Box 5 (TBX5)

适用

  • 34
  • 14
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
人, 犬

宿主

  • 31
  • 3
  • 1

克隆类型

  • 32
  • 3
多克隆

标记

  • 21
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This T-Box 5 antibody is un-conjugated

应用范围

  • 28
  • 16
  • 15
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TBX5.
  • 应用备注

    TBX5 antibody can be used for detection of TBX5 by ELISA at 1:62500. TBX5 antibody can be used for detection of TBX5 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store TBX5 antibody at -20 °C.
  • 抗原

    T-Box 5 (TBX5)

    别名

    TBX5

    背景

    TBX5 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs.

    分子量

    39 kDa

    基因ID

    6910

    NCBI登录号

    NP_542449

    UniProt

    Q99593
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