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T-Box 5 Protein (TBX5) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

TBX5 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2733312
发货至: 中国
  • 抗原 See all T-Box 5 (TBX5) 蛋白
    T-Box 5 (TBX5)
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 3
    • 2
    • 1
    • 1
    资源
    • 2
    • 2
    • 2
    • 1
    HEK-293 Cells
    标记
    This T-Box 5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human TBX5 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product TBX5 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    T-Box 5 (TBX5)
    别名
    Tbx5 (TBX5 产品)
    别名
    TBX5 Protein, tbx-5 Protein, xtbx-5 Protein, xtbx5 Protein, tbx5 Protein, HOS Protein, tbx5.1 Protein, zTbx5 Protein, zf-tbx5 Protein, T-box 5 Protein, T-box 5 L homeolog Protein, T-box 5a Protein, TBX5 Protein, tbx5 Protein, tbx5.L Protein, Tbx5 Protein, tbx5a Protein
    背景
    This gene 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. Several transcript variants encoding different isoforms have been described for this gene.
    分子量
    57.5 kDa
    NCBI登录号
    NP_000183
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