GFAP recombinant monoclonal antibody, clone 14C8

Catalog # RAB07733

Size

Price

Stock

Quantity

Size:100 uL
Price: USD $ 638.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Flow Cytometry
Application

Flow Cytometry

Overlay Peak curve showing Hela cells stained with GFAP recombinant monoclonal antibody, clone 14C8 (red line) at 1:50.

  • Specification

    Product Description

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

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against a synthetic peptide corresponding to human GFAP.

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity chromatography purification

    Isotype

    IgG

    Recommend Usage

    ELISA
    Flow Cytometry(1:50-1:200)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH7.4 (150 mM NaCl, 0.02% sodium azide and 50% glycerol)

    Storage Instruction

    Store at -20°C or -80°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

    Enzyme-linked Immunoabsorbent Assay

    Flow Cytometry

    Overlay Peak curve showing Hela cells stained with GFAP recombinant monoclonal antibody, clone 14C8 (red line) at 1:50.
  • Gene Info — GFAP

    Entrez GeneID

    2670

    Protein Accession#

    P14136

    Gene Name

    GFAP

    Gene Alias

    FLJ45472

    Gene Description

    glial fibrillary acidic protein

    Omim ID

    137780 203450

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq

    Other Designations

    -

  • 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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