GFAP Antibody

Cat no: 251752

Supplier: ABBIOTEC

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Description
Additional Information

Glial fibrillary acidic protein (GFAP), a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells. Defects in GFAP are a cause of Ale, Xenopus/Amphibian,ander disease (ALE, Xenopus/Amphibian,D). Ale, Xenopus/Amphibian,ander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes.

Catalogue number:	251752
Reactivities:	Human, Mouse, Porcine, Rabbit
Applications:	Immunohistochemistry
Size:	0.1 mg
Accession:	P14136
Antigen:	GFAP from pig spinal cord.
Format:	Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4, 2% BSA with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
P type:	Mouse Monoclonal Antibody
Isotype:	Mouse IgG1
Clonality:	GA-8
Additional info:	Glial fibrillary acidic protein; GFAP