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Anti-GFAP Antibody (clone G-A-5) LS-C347458

Catalog Size Price
LS-C347458-100 100 µg (1 mg/ml) Unavailable

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100% Guaranteed
Mouse Monoclonal [clone G-A-5] (IgG1) to Human GFAP
Human, Mouse, Rat, Pig, Chicken
IHC - Paraffin, IHC - Frozen, ICC, Western blot
Unconjugated

Details

Human GFAP
Mouse
Human, Mouse, Rat, Pig, Chicken (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [G-A-5]
Unconjugated
Purified
Unmodified

Applications

  • IHC - Paraffin
  • IHC - Frozen
  • ICC
  • Western blot

Specificity and Use

GFAP antibody was raised against g-A-5 is a mouse monoclonal IgG1 antibody derived by fusion of PA1 mouse myeloma cells with spleen cells from BALB/c mice immunized with purified GFAP from porcine spinal cord.
Recognizes GFAP in human, mouse, rat, porcine and chicken. The antibody reacts with the carboxyterminal cys II fragment of GFAP as determined by western blotting and does not cross react with vimentin.
Glial fibrillary acidic protein(GFAP) is a class III intermediate filament protein, a cytoskeletal protein that is located within the cytoplasm of astrocyctes and other glial cells e. g. Schwann cells and ependymal cells. In the central nervous system, GFAP is the major intermediate filament protein of mature astrocytes. GFAP plays an important role in maintaining the structure and stability of astrocytes during development and has also been shown to be involved in cellular communication, motility and mitosis. Mutations in GFAP give rise to Alexander disease, a rare and fatal disease of the central nervous system. Antibodies recognizing GFAP are commonly used to identify cells of astrocytic origin under normal and pathological conditions.

Packaging

PBS, 0.09% sodium azide.
Store at 4°C, or in small aliquots at -20°C.
For research use only.

About GFAP

P14136 NM_002055 NP_002046.1

GFAP Antibody

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.

Requested From: 
Date Requested: 12/15/2017

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