GFAP Mouse Monoclonal Antibody [Clone ID: GA5]

CAT#: AM32829PU-S

GFAP mouse monoclonal antibody, clone GA5, Purified

Size: 20 ug 100 ug


USD 570.00

2 Weeks*

Size
    • 100 ug

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Specifications

Product Data
Clone Name GA5
Applications FC, IF, IHC, IP, WB
Recommended Dilution ELISA: Use Antibody without BSA for Coating.
Western Blot:
 0.5-1 µg/ml. 
Flow Cytometry: 0.5-1 µg/106 cells. 
Immunofluorescence: 1-2 µg/ml.
Immunoprecipitation: 1-2 µg/500 µg protein lysate. 
Immunohistochemistry on Cryo Sections:
0.5-1 µg/ml  (See also Tobin et. al. for details).
Immunohistochemistry on Paraffin Sections: 0.5-1 µg/ml for 30 minutes at RT.
Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Citrate Buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes.
Recommended Positive Control: Brain or Astrocytoma.
Reactivities Bovine, Chicken, Human, Mouse, Porcine, Rabbit, Rat
Host Mouse
Isotype IgG1
Clonality Monoclonal
Immunogen Glial Fibrillary Protein from Porcine spinal cord
Specificity This Monoclonal antibody recognizes a protein of ~50kDa which is identified as Glial Fibrillary Acidic Protein (GFAP). It shows no cross-reaction with other intermediate filament proteins. 
It labels some astrocytes and some CNS ependymal cells but not oligodendrocytes or neurons.
Antibody to GFAP is useful in differentiating primary gliomas from metastatic lesions in the brain and for documenting astrocytic differentiation in tumors outside the CNS.
Cellular Localization: Cytoplasmic.
Formulation 10mM PBS
State: Purified
State: Liquid purified IgG fraction from Bioreactor Concentrate
Stabilizer: 0.05% BSA
Preservative: 0.05% Sodium Azide
Concentration lot specific
Purification Affinity Chromatography on Protein A/G
Conjugation Unconjugated
Storage Store undiluted at 2-8°C.
Stability Shelf life: one year from despatch.
Predicted Protein Size ~50 kDa
Gene Name glial fibrillary acidic protein
Background Glial fibrillary acidic protein (GFAP) is a class-III intermediate-filament (IF) protein that is highly specific for cells of astroglial lineage, although its tissue-specific role is speculative. 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. The gene is localized to chromosome 17q21. Alternate splicing of this gene generates several transcript variants encoding three different isoforms.
Synonyms Glial Fibrillary Acidic Protein
Reference Data

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