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Gephyrin (GPHN) (N-Term) Peptide

GPHN 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN977588
发货至: 中国

Quick Overview for Gephyrin (GPHN) (N-Term) Peptide (ABIN977588)

抗原

Gephyrin (GPHN)

宿主

资源

  • 4
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB)
  • 蛋白结构域

    N-Term

    产品特性

    This is a synthetic peptide designed for use in combination with anti-GPHN antibody (Catalog #: ARP51838_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    纯化方法

    Purified
  • 应用备注

    Each Investigator should determine their own optimal working dilution for specific applications.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    浓度

    1 mg/mL

    缓冲液

    Final peptide concentration is 1 mg/mL in PBS.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原

    Gephyrin (GPHN)

    背景

    GPHN is 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 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. 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.

    Alias Symbols: GEPH, GPH, GPHRYN, KIAA1385

    Protein Interaction Partner: ARHGEF9,DYNLL1,DYNLL2,ENAH,GABARAP,GLRB,GPHN,MTOR,PFN1,PIN1,TUBA4A,ARHGEF9,GLRB,MTOR,Mtor,OTUD4,PFN1,PRPF4

    Protein Size: 736

    分子量

    80 kDa

    基因ID

    10243

    NCBI登录号

    NM_001024218, NP_001019389

    UniProt

    Q9NQX3
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