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TMEM176A 抗体

TMEM176A 适用: 大鼠 IF, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7075995
发货至: 中国
  • 抗原 See all TMEM176A products
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    适用
    • 15
    • 15
    • 7
    • 1
    大鼠
    宿主
    • 21
    • 1
    克隆类型
    • 21
    • 1
    多克隆
    标记
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TMEM176A antibody is un-conjugated
    应用范围
    • 22
    • 13
    • 13
    • 5
    • 4
    • 3
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
    交叉反应
    大鼠
    纯化方法
    Affinity purification
    免疫原
    KLH conjugated Synthetic peptide corresponding to Mouse TMEM176A
  • 应用备注
    IHC/IF (R) 1:500-1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS, pH 7.4, 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
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    别名
    TMEM176A (TMEM176A 产品)
    别名
    GS188 antibody, HCA112 antibody, 0610011I04Rik antibody, AU040201 antibody, AU041743 antibody, Keg2 antibody, 0610011i04rik antibody, RGD1310725 antibody, CL1 antibody, transmembrane protein 176A antibody, TMEM176A antibody, Tmem176a antibody
    背景
    TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
    基因ID
    66058
    UniProt
    Q9DCS1
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