GFAP monoclonal antibody, clone SB61b (Biotin)

Catalog # MAB5898

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Price

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Quantity

Size:500 ug
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunofluorescence
Application

Immunofluorescence

The CCF-STTG1 cell line was fixed with 5% acetic acid methanol solution for 30 minutes followed by 5% bovine serum PBS blocking. Cells were permeabilized by 0.1% Triton X PBS for 15 minutes prior to staining with GFAP monoclonal antibody, clone SB61b (CY3) (Cat # MAB5899). Cells were then fixed and the slide was mounted with DAPI-Fluormount-G.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against recombinant GFAP.

    Immunogen

    Recombinant protein corresponding to human GFAP.

    Host

    Mouse

    Reactivity

    Human

    Specificity

    human GFAP (~ 50 KDa).

    Form

    Liquid

    Conjugation

    Biotin

    Isotype

    IgG2b, kappa

    Recommend Usage

    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS (0.09% sodium azide)

    Storage Instruction

    Store at 4°C.

    Note

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

  • Applications

    Western Blot

    Immunohistochemistry (Frozen sections)

    Immunofluorescence

    The CCF-STTG1 cell line was fixed with 5% acetic acid methanol solution for 30 minutes followed by 5% bovine serum PBS blocking. Cells were permeabilized by 0.1% Triton X PBS for 15 minutes prior to staining with GFAP monoclonal antibody, clone SB61b (CY3) (Cat # MAB5899). Cells were then fixed and the slide was mounted with DAPI-Fluormount-G.
  • Gene Info — GFAP

    Entrez GeneID

    2670

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