GFAP polyclonal antibody

Catalog # PAB7137

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Price

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Quantity

Size:100 ug
Price: USD $ 428.00
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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 (Tissue lysate)
Application

Western Blot (Tissue lysate)

GFAP polyclonal antibody (Cat # PAB7137) (0.01 ug/mL) staining of Human Cerebellum (1), Mouse Brain (2) and (0.003 ug/mL) Rat Brain (3) lysate (35 ug protein in RIPA buffer). Detected by chemiluminescence.

  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of GFAP.

    Immunogen

    A synthetic peptide corresponding to C-terminus of human GFAP.

    Sequence

    C-DGEVIKESKQEHKD

    Host

    Goat

    Theoretical MW (kDa)

    49.9

    Reactivity

    Human, Mouse, Rat

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:32000)
    Western Blot (0.001-0.01 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)

    Storage Instruction

    Store at -20°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

    Western Blot (Tissue lysate)

    GFAP polyclonal antibody (Cat # PAB7137) (0.01 ug/mL) staining of Human Cerebellum (1), Mouse Brain (2) and (0.003 ug/mL) Rat Brain (3) lysate (35 ug protein in RIPA buffer). Detected by chemiluminescence.
  • Gene Info — GFAP

    Entrez GeneID

    2670

    Protein Accession#

    NP_002046.1

    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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