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Gephyrin antibody (AA 288-735)

The Rabbit Polyclonal anti-Gephyrin antibody is suitable to detect Gephyrin in samples from Zebrafish (Danio rerio). It has been validated for WB and IHC (p).
Catalog No. ABIN7873329
$743.31
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Gephyrin antibody (AA 288-735) (ABIN7873329)

Target

See all Gephyrin (GPHN) Antibodies
Gephyrin (GPHN)

Reactivity

  • 86
  • 46
  • 41
  • 6
  • 4
  • 4
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  • 3
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  • 2
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Zebrafish (Danio rerio)

Host

  • 60
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  • 2
  • 1
Rabbit

Clonality

  • 50
  • 43
Polyclonal

Conjugate

  • 50
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This Gephyrin antibody is un-conjugated

Application

  • 60
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  • 7
  • 5
  • 2
  • 1
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 20
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    • 7
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    • 1
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    AA 288-735

    Purpose

    Zebrafish Gephyrin Antibody / Gphna / Gphnb

    Purification

    Antigen affinity chromatography

    Immunogen

    An E.coli-derived zebrafish GPHNa/b recombinant protein (amino acids V288-L735) was used as the immunogen for the Zebrafish Gephyrin antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal dilution of the Zebrafish Gephyrin antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Zebrafish Gephyrin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Gephyrin (GPHN)

    Alternative Name

    Gephyrin

    Background

    Gephyrin is a protein that in humans is encoded by the GPHN gene. 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.

    UniProt

    D3KYK7

    Pathways

    Synaptic Membrane, Skeletal Muscle Fiber Development
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