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Gephyrin 抗体

This anti-Gephyrin antibody is a 兔 多克隆 antibody detecting Gephyrin in WB 和 ELISA. Suitable for 人.
产品编号 ABIN7228650
发货至: 中国

Quick Overview for Gephyrin 抗体 (ABIN7228650)

抗原

See all Gephyrin (GPHN) 抗体
Gephyrin (GPHN)

适用

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宿主

  • 57
  • 30
  • 2
  • 1
  • 1

克隆类型

  • 49
  • 42
多克隆

标记

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This Gephyrin antibody is un-conjugated

应用范围

  • 58
  • 44
  • 30
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Western Blotting (WB), ELISA
  • 原理

    GEPH Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of GEPH protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human GEPH protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    储存方法

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    Gephyrin (GPHN)

    别名

    GEPH

    背景

    Rabbit Anti-GEPH Polyclonal Antibody,Gephyrin, Molybdopterin adenylyltransferase, MPT adenylyltransferase, Domain G, Molybdopterin molybdenumtransferase, MPT Mo-transferase, Domain E,GPHN 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.,GEPH

    分子量

    observerd band 80kDa

    基因ID

    10243

    UniProt

    Q9NQX3

    途径

    Synaptic Membrane, Skeletal Muscle Fiber Development
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