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WDR4 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

WDR4 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 ABIN2735513
发货至: 中国
  • 抗原 See all WDR4 蛋白
    WDR4 (WD Repeat Domain 4 (WDR4))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 2
    宿主
    • 2
    • 1
    • 1
    • 1
    • 1
    资源
    • 4
    • 1
    • 1
    HEK-293 Cells
    标记
    This WDR4 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human WDR4 (transcript variant 2) 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 WDR4 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
    WDR4 (WD Repeat Domain 4 (WDR4))
    别名
    Wdr4 (WDR4 产品)
    别名
    TRM82 Protein, TRMT82 Protein, AI415180 Protein, AI448349 Protein, D530049K22Rik Protein, WD repeat domain 4 Protein, WD repeat domain 4 S homeolog Protein, WDR4 Protein, Wdr4 Protein, wdr4.S Protein
    背景
    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene.
    分子量
    45.3 kDa
    NCBI登录号
    NP_387510
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