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TMEM176B 抗体 (AA 25-150)

TMEM176B 适用: 人 ELISA, ICC, IF (cc), IF (p), IHC (fro), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385213
发货至: 中国
  • 抗原 See all TMEM176B 抗体
    TMEM176B (Transmembrane Protein 176B (TMEM176B))
    抗原表位
    • 5
    • 2
    • 1
    AA 25-150
    适用
    • 9
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 9
    克隆类型
    • 9
    多克隆
    标记
    • 5
    • 2
    • 1
    • 1
    This TMEM176B antibody is un-conjugated
    应用范围
    ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human LR8/TMEM176B
    亚型
    IgG
    Top Product
    Discover our top product TMEM176B Primary Antibody
  • 应用备注
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    TMEM176B (Transmembrane Protein 176B (TMEM176B))
    别名
    LR8/TMEM176B (TMEM176B 产品)
    别名
    MGC165671 antibody, LR8 antibody, 1810009M01Rik antibody, Clast1 antibody, Lr8 antibody, Torid antibody, transmembrane protein 176B antibody, TMEM176B antibody, Tmem176b antibody
    背景

    Synonyms: LR 8, TMEM176B, Transmembrane protein 176B, T176B_HUMAN.

    Background: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 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. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The LR8 gene product has been provisionally designated LR8 pending further characterization.

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