• Target：
• GFAP

• Fields：
• >>JAK-STAT signaling pathway

• Gene Name：
• GFAP

• Protein Name：
• Glial fibrillary acidic protein (GFAP)

• Sequence：
• P14136

• Human Gene Id：
• 2670

• Human Swiss Prot No：
• P14136

• Mouse Gene Id：
• 14580

• Mouse Swiss Prot No：
• P03995

• Rat Gene Id：
• 24387

• Rat Swiss Prot No：
• P47819

• Immunogen：
• Synthesized peptide derived from human GFAP (Phospho Ser13)

• Specificity：
• This antibody detects endogenous levels of GFAP (Phospho Ser13) Rabbit pAb at Human, Mouse,Rat

• Formulation：
• Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

• Source：
• Rabbit,polyclonal

• Dilution：
• WB 1:500-2000 IHC 1:50-200

• Purification：
• The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Other Name：
• Glial fibrillary acidic protein (GFAP)

• Observed Band(KD)：
• 45kD

• Background：
• glial fibrillary acidic protein(GFAP) Homo sapiens 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, Oct 2008],

• Function：
• alternative products:Isoforms differ in the C-terminal region which is encoded by alternative exons,disease:Defects in GFAP are a cause of Alexander disease (ALEXD) [MIM:203450]. Alexander 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. The most common form affects infants and young children, and is characterized by progressive failure of central myelination, usually leading to death usually within the first decade. Infants with Alexander disease develop a leukoencephalopathy with macrocephaly, seizures, and psychomotor retardation. Patients with juvenile or adult forms typically experience ataxia, bulbar signs and spasticity, and a more slowly progressive course.,function:GFAP, a class-III intermediate filament, is a cell-spe

• Subcellular Location：
• Cytoplasm . Associated with intermediate filaments. .

• Expression：
• Expressed in cells lacking fibronectin.

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