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BAIAP2 抗体

This anti-BAIAP2 antibody is a 小鼠 单克隆 antibody detecting BAIAP2 in WB, IHC, IF 和 FACS. Suitable for 人.
产品编号 ABIN2716509
发货至: 中国

Quick Overview for BAIAP2 抗体 (ABIN2716509)

抗原

See all BAIAP2 抗体
BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))

适用

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宿主

  • 46
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小鼠

克隆类型

  • 48
  • 7
单克隆

标记

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This BAIAP2 antibody is un-conjugated

应用范围

  • 44
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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

克隆位点

1D9
  • 产品特性

    Homo sapiens BAI1-associated protein 2 (BAIAP2), transcript variant 3

    纯化方法

    Purified from mouse ascites fluids by affinity chromatography

    免疫原

    Full length human recombinant protein of human BAIAP2 (NP_006331) produced in HEK293T cell.

    亚型

    IgG1
  • 应用备注

    WB 1:2000, IHC 1:150, 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

    BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))

    别名

    BAIAP2

    背景

    The protein encoded by this gene has been identified as a brain-specific angiogenesis inhibitor (BAI1)-binding protein. This adaptor protein links membrane bound G-proteins to cytoplasmic effector proteins. This protein functions as an insulin receptor tyrosine kinase substrate and suggests a role for insulin in the central nervous system. It also associates with a downstream effector of Rho small G proteins, which is associated with the formation of stress fibers and cytokinesis. This protein is involved in lamellipodia and filopodia formation in motile cells and may affect neuronal growth-cone guidance. This protein has also been identified as interacting with the dentatorubral-pallidoluysian atrophy gene, which is associated with an autosomal dominant neurodegenerative disease. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    分子量

    57.3 kDa

    基因ID

    10458

    NCBI登录号

    NM_006340

    HGNC

    10458
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