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WDR4 抗体

WDR4 适用: 人 WB, IF, FACS 宿主: 小鼠 Monoclonal 4G1 unconjugated
产品编号 ABIN2735512
发货至: 中国
  • 抗原 See all WDR4 抗体
    WDR4 (WD Repeat Domain 4 (WDR4))
    适用
    • 35
    • 12
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 33
    • 2
    小鼠
    克隆类型
    • 32
    • 3
    单克隆
    标记
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WDR4 antibody is un-conjugated
    应用范围
    • 27
    • 15
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
    产品特性
    Homo sapiens WD repeat domain 4 (WDR4), transcript variant 2
    纯化方法
    Purified from mouse ascites fluids by affinity chromatography
    免疫原
    Full length human recombinant protein of human WDR4(NP_387510) produced in HEK293T cell.
    克隆位点
    4G1
    亚型
    IgG1
    Top Product
    Discover our top product WDR4 Primary Antibody
  • 应用备注
    WB 1:2000, IF 1:100, FLOW 1:100,
    说明

    The concentration of the product may vary between diferrent lots.

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5-1.0 mg/mL
    缓冲液
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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
    -20 °C
  • 抗原
    WDR4 (WD Repeat Domain 4 (WDR4))
    别名
    WDR4 (WDR4 产品)
    别名
    TRM82 antibody, TRMT82 antibody, AI415180 antibody, AI448349 antibody, D530049K22Rik antibody, WD repeat domain 4 antibody, WD repeat domain 4 S homeolog antibody, WDR4 antibody, Wdr4 antibody, wdr4.S antibody
    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. Two transcript variants encoding the same protein have been found for this gene.
    分子量
    45.3 kDa
    基因ID
    10785
    NCBI登录号
    NM_033661
    HGNC
    10785
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