GPHN recombinant monoclonal antibody, clone R06-8G4

Catalog # RAB05245

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Price

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Quantity

Size:100 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against human Gephyrin.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against recombinant protein corresponding to human Gephyrin

    Theoretical MW (kDa)

    Calculated MW: 80 kD

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunofluorescence (1/50-1/200)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)(1/50-1/100)
    Western Blot (1/500-1/1000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, 150 mM NaCl, pH 7.4 (50% glycerol and 0.02% Sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunocytochemistry

    Immunofluorescence

  • Gene Info — GPHN

    Entrez GeneID

    10243

    Gene Name

    GPHN

    Gene Alias

    GEPH, GPH, GPHRYN, KIAA1385

    Gene Description

    gephyrin

    Omim ID

    149400 252150 603930

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    OTTHUMP00000028393

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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