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SOX10 Protein (Myc-DYKDDDDK Tag)

SOX10 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 ABIN2732430
发货至: 中国
  • 抗原 See all SOX10 蛋白
    SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))
    蛋白类型
    Recombinant
    宿主
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    资源
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    HEK-293 Cells
    标记
    This SOX10 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human SOX10 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 SOX10 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
    SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))
    别名
    Sox10 (SOX10 产品)
    别名
    DOM Protein, PCWH Protein, WS2E Protein, WS4 Protein, WS4C Protein, SOX-10 Protein, SOX10 Protein, dom Protein, ws4 Protein, Dom Protein, Sox21 Protein, SOX9 Protein, cls/sox10 Protein, zgc:100757 Protein, SRY-box 10 Protein, SRY box 10 Protein, SRY-box 10 L homeolog Protein, SRY (sex determining region Y)-box 10 Protein, SOX10 Protein, Sox10 Protein, sox10.L Protein, sox10 Protein
    背景
    This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease.
    分子量
    49.7 kDa
    NCBI登录号
    NP_008872
    途径
    Chromatin Binding
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