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TMEM176B 抗体 (AA 25-150)

This anti-TMEM176B antibody is a 兔 多克隆 antibody detecting TMEM176B in ELISA, ICC, IF (cc), IF (p), IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN1385213
发货至: 中国

Quick Overview for TMEM176B 抗体 (AA 25-150) (ABIN1385213)

抗原

See all TMEM176B 抗体
TMEM176B (Transmembrane Protein 176B (TMEM176B))

适用

  • 11
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1

宿主

  • 11

克隆类型

  • 11
多克隆

标记

  • 7
  • 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))
  • 抗原表位

    • 6
    • 3
    • 1
    AA 25-150

    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
  • 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

    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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