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T-Box 5 抗体

TBX5 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 7B11 unconjugated
产品编号 ABIN969432
发货至: 中国
  • 抗原 See all T-Box 5 (TBX5) 抗体
    T-Box 5 (TBX5)
    适用
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    宿主
    • 35
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    • 1
    小鼠
    克隆类型
    • 36
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    单克隆
    标记
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    This T-Box 5 antibody is un-conjugated
    应用范围
    • 31
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    • 3
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    • 1
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    Western Blotting (WB), ELISA
    原理
    TBX5 Antibody
    纯化方法
    Ascitic fluid
    免疫原
    Purified recombinant fragment of TBX5 expressed in E. Coli.
    克隆位点
    7B11
    亚型
    IgG1
    Top Product
    Discover our top product TBX5 Primary Antibody
  • 应用备注
    ELISA: 1/10000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Ascitic fluid containing 0.03 % 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 short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Collavoli, Hatcher, He, Okin, Deo, Basson: "TBX5 nuclear localization is mediated by dual cooperative intramolecular signals." in: Journal of molecular and cellular cardiology, Vol. 35, Issue 10, pp. 1191-5, (2003) (PubMed).

  • 抗原
    T-Box 5 (TBX5)
    别名
    TBX5 (TBX5 产品)
    别名
    TBX5 antibody, tbx-5 antibody, xtbx-5 antibody, xtbx5 antibody, tbx5 antibody, HOS antibody, tbx5.1 antibody, zTbx5 antibody, zf-tbx5 antibody, T-box 5 antibody, T-box 5 L homeolog antibody, T-box 5a antibody, TBX5 antibody, tbx5 antibody, tbx5.L antibody, Tbx5 antibody, tbx5a antibody
    背景

    Description: TBX5, also known as T-box 5. It 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. It is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The TBX5 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. Several transcript variants encoding different isoforms have been described for this gene.

    Aliases: HOS, TBX5

    分子量
    53kDa
    基因ID
    6910
    HGNC
    6910
    UniProt
    Q99593
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