GFAP monoclonal antibody (M02), clone 2E9

Catalog # H00002670-M02

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Size:100 ug
Price: USD $ 335.00
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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
Western Blot (Transfected lysate)
Application

Western Blot (Transfected lysate)

Western Blot analysis of GFAP expression in transfected 293T cell line by GFAP monoclonal antibody (M02), clone 2E9.

Lane 1: GFAP transfected lysate (Predicted MW: 49.9 KDa).
Lane 2: Non-transfected lysate.

QC Test

Western Blot detection against Immunogen (36.74 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant GFAP.

    Immunogen

    GFAP (AAH41765, 131 a.a. ~ 230 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    TANSARLEVERDNLAQDLATVRQKLQDETNLRLEAENNLAAYRQEADEATLARLDLERKIESLEEEIRFLRKIHEEEVRELQEQLARQQVHVELDVAKPD

    Host

    Mouse

    Reactivity

    Human

    Isotype

    IgG2b Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.74 KDa) .

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Transfected lysate)

    Western Blot analysis of GFAP expression in transfected 293T cell line by GFAP monoclonal antibody (M02), clone 2E9.

    Lane 1: GFAP transfected lysate (Predicted MW: 49.9 KDa).
    Lane 2: Non-transfected lysate.

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — GFAP

    Entrez GeneID

    2670

    GeneBank Accession#

    BC041765

    Protein Accession#

    AAH41765

    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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