GeneBio Systems
Anti-GFAP Antibody (Monoclonal, G-A-5)
Anti-GFAP Antibody (Monoclonal, G-A-5)
SKU:MA1045
Couldn't load pickup availability
Size: 100 μg
Storage: Store at -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freeze-thaw cycles.
Form: Lyophilized
Reactivity: Human,Mouse,Pig,Rat
Applications: IF,IHC,IHC-F,WB
Application Details: Western blot, 0.5-1μg/ml, Human, mouse, pig, rat
Immunohistochemistry (Paraffin-embedded Section), 0.4-1μg/ml, Human, pig, rat
Immunohistochemistry (Frozen Section), 0.5-1μg/ml, Human, pig, rat, -
Immunofluorescence, 2μg/ml, Rat
Gene Name: GFAP
Specificity: No cross reactivity with other proteins.
Background: Glial fibrillary acidic protein (GFAP) is an intermediate filament protein of 52Kda. GFAP gene is mapped to human 17q21. GFAP is a useful marker of astroglia in the brain. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.
Immunogen: GFAP from pig spinal cord.
Clonality: Monoclonal
Contents: Mouse IgG in stabilizing components, 1.2% sodium acetate and 0.01mg NaN3.
*This antibody is supplied in a stabilized formulation.
Compatibility with conjugation reactions depends on the chemistry of the conjugation method used.
For conjugation methods that are not compatible with the stabilizing components present in this formulation, a carrier-free antibody format is required.
Purification: Ascites
Reconstitution: Add 1ml of PBS buffer will yield a concentration of 100ug/ml.
Reference: 1. Brenner, M.; Johnson, A. B.; Boespflug-Tanguy, O.; Rodriguez, D.; Goldman, J. E.; Messing, A. : Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nature Genet. 27: 117-120, 2001. 2. Rodriguez, D.; Gauthier, F.; Bertini, E.; Bugiani, M.; Brenner, M.; N'guyen, S.; Goizet, C.; Gelot, A.; Surtees, R.; Pedespan, J.-M.; Hernandorena, X.; Troncoso, M.; Uziel, G.; Messing, A.; Ponsot, G.; Pham-Dinh, D.; Dautigny, A.; Boespflug-Tanguy, O. : Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation. Am. J. Hum. Genet. 69: 1134-1140, 2001. Note: Erratum: Am. J. Hum. Genet. 69: 1413 only, 2001.
Uniprot ID: P47819
Host: Mouse
Concentration: Adding 1 ml of PBS buffer will yield a concentration of 100 μg/ml.
Conjugate:
Cross Reactivity: No cross-reactivity with other proteins
Isotype: Mouse IgG1
Phospho_site:
Clone Number: Clone: G-A-5
Observed Molecular Weight: 50 kDa
Calculated Molecular Weight: 49957 MW
Gene ID: Human(2670), Mouse(14580), Rat(24387)
Protein Name: Glial fibrillary acidic protein
Gene Full Name: glial fibrillary acidic protein
Synonyms: FLJ45472; intermediate filament protein
