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Gephyrin 抗体

This anti-Gephyrin antibody is a 兔 多克隆 antibody detecting Gephyrin in WB, IF, IP, IHC (p), ICC 和 IHC (fro). Suitable for 人.
产品编号 ABIN7466988
发货至: 中国

Quick Overview for Gephyrin 抗体 (ABIN7466988)

抗原

See all Gephyrin (GPHN) 抗体
Gephyrin (GPHN)

适用

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宿主

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克隆类型

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多克隆

标记

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This Gephyrin antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human Gephyrin. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:10000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. IHC-Fr: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: NIH-3T3 , JC

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.32 mg/mL

    缓冲液

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Gephyrin (GPHN)

    别名

    gephyrin

    背景

    Gephyrin , GEPH , GPH , GPHRYN , HKPX1 , MOCODC,This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described, however, the full-length nature of all transcript variants is not currently known. [provided by RefSeq]

    分子量

    80 kDa

    基因ID

    10243

    UniProt

    Q9NQX3

    途径

    Synaptic Membrane, Skeletal Muscle Fiber Development
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