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SOX18 Protein (Myc-DYKDDDDK Tag)

SOX18 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 ABIN2732448
发货至: 中国
  • 抗原 See all SOX18 蛋白
    SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))
    蛋白类型
    Recombinant
    宿主
    • 3
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    • 1
    • 1
    • 1
    资源
    • 3
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    HEK-293 Cells
    标记
    This SOX18 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human SOX18 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 SOX18 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
    SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))
    别名
    Sox18 (SOX18 产品)
    别名
    HLTS Protein, AI385749 Protein, Ra Protein, Ragl Protein, sox18 Protein, xSox18alpha Protein, xSox18beta Protein, xsox18 Protein, SRY-box 18 Protein, SRY (sex determining region Y)-box 18 Protein, SRY box 18 Protein, SRY-box 18 S homeolog Protein, SRY-box 18 L homeolog Protein, SRY box 1 Protein, SOX18 Protein, Sox18 Protein, sox18.S Protein, sox18.L Protein, Sox1 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 regulator after forming a protein complex with other proteins. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
    分子量
    40.7 kDa
    NCBI登录号
    NP_060889
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