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Neuroligin 3 antibody (AA 601-700) (HRP)

The Rabbit Polyclonal anti-Neuroligin 3 antibody has been validated for ELISA, IHC (p) and IHC (fro). It is suitable to detect Neuroligin 3 in samples from Mouse.
Catalog No. ABIN1407650

Quick Overview for Neuroligin 3 antibody (AA 601-700) (HRP) (ABIN1407650)

Target

See all Neuroligin 3 (NLGN3) Antibodies
Neuroligin 3 (NLGN3)

Reactivity

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  • 2
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  • 1
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Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Neuroligin 3 antibody is conjugated to HRP

Application

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ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Binding Specificity

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    AA 601-700

    Cross-Reactivity

    Mouse

    Predicted Reactivity

    Human,Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human Neuroligin 3

    Isotype

    IgG
  • Application Notes

    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Handling Advice

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    Neuroligin 3 (NLGN3)

    Alternative Name

    Neuroligin 3

    Background

    Synonyms: Gliotactin homolog, Neuroligin3, Neuroligin-3, Nlgn3, NLGN3_HUMAN.

    Background: This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. Mutations in this gene may be associated with autism and Asperger syndrome. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Oct 2009].

    Pathways

    Synaptic Membrane
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