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Anti-GFAP Purified

GFAP (glial fibrillary acidic protein) was discovered by Bignami et al. (1972) as a major fibrous protein of multiple sclerosis plaques. It was subsequently found to be a member of the 10 nm or intermediate filament protein family, specifically the intermediate filament protein family class III, which also includes peripherin, desmin and vimentin. GFAP is heavily, and specifically, expressed in astrocytes and certain other astroglia in the central nervous system, in satellite cells in peripheral ganglia, and in non-myelinating Schwann cells in peripheral nerves. In addition, neural stem cells frequently strongly express GFAP. It is also found in the lens epithelium, Kupffer cells of the liver, in some cells in salivary tumors and has been reported in erythrocytes. Although its function is not fully understood, GFAP protein is probably involved in controlling the shape and movement of astrocytes. The protein probably also plays a significant role in the interactions of astrocytes with other cells, which are required for the formation and maintenance of the insulating layer (myelin) that covers nerve cells. Additionally, GFAP protein may assist in maintaining the protective barrier that allows only certain substances to pass between blood vessels and the brain (blood-brain barrier) .In adults, GFAP levels increase as a result of the proliferation of astrocytes that occurs in a response to a variety of physical, chemical and etiological insults, including Alzheimer’ s disease, epilepsy and multiple sclerosis.Antibodies to GFAP are therefore very useful as markers of astrocytic cells and neural stem cells and for distinguishing of neoplasms of astrocytic origin from other neoplasms in the central nervous system. Finally, Alexander's disease was recently shown to be caused by point mutations in protein coding region of the GFAP gene (Brenner et al., 2001) . All forms of Alexander disease are characterized by the presence of Rosenthal fibers, which are GFAP containing cytoplasmic inclusions found in astrocytes.

Product Specifications

Certification

RUO

Reactivity

Pig, Human, Rat

Immunogen

Porcine spinal cord

Target Antigen

GFAP

Clone

GA-5

Applications

IP, WB, IHC-P, ICC

Concentration

1 mg/mL

Format

Purified

Buffer

Phosphate buffered saline (PBS), pH 7.4, 15 mM sodium azide

References & Citations

*Rungger-Brändle E, Dosso AA, Leuenberger PM: Glial reactivity, an early feature of diabetic retinopathy. Invest Ophthalmol Vis Sci. 2000 Jun;41 (7) :1971-80., URL: https://www.ncbi.nlm.nih.gov/pubmed/10845624?itool, *Guillemin GJ, Wang L, Brew BJ: Quinolinic acid selectively induces apoptosis of human astrocytes: potential role in AIDS dementia complex. J Neuroinflammation. 2005 Jul 26;2:16. , URL: https://www.ncbi.nlm.nih.gov/pubmed/16042813?itool, *Joardar A, Sen AK, Das S: Docosahexaenoic acid facilitates cell maturation and beta-adrenergic transmission in astrocytes. J Lipid Res. 2006 Mar;47 (3) :571-81. , URL: http://www.ncbi.nlm.nih.gov/pubmed/16352524?itool=, *Triviño A, Ramírez JM, Ramírez AI, Salazar JJ, García-Sanchez J: Retinal perivascular astroglia: an immunoperoxidase study. Vision Res. 1992 Sep;32 (9) :1601-7., URL: https://www.ncbi.nlm.nih.gov/pubmed/1455732?ordina, *Perng MD, Cairns L, van den IJssel P, Prescott A, Hutcheson AM, Quinlan RA: Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin. J Cell Sci. 1999 Jul;112 (Pt 13) :2099-112., URL: https://www.ncbi.nlm.nih.gov/pubmed/10362540?itool

Other References

*Brenner M, Johnson AB, Boespflug-Tanguy O, Rodriguez D, Goldman JE, Messing A: Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet. 2001 Jan;27 (1) :117-20., URL: https://pubmed.ncbi.nlm.nih.gov/11138011/

Storage Conditions

Store at 2-8°C. Do not freeze.

Specificity

The mouse monoclonal antibody GA-5 reacts with GFAP, the principal marker of astroglial cells in the central nervous system, which is specifically expressed in satellite cells in peripheral ganglia and in non myelinating Schwann cells in peripheral nerves. The GFAP protein runs on gels at ~55 kDa protein, usually associated with lower Mw bands which are thought to be proteolytic fragments and alternate transcripts from the single gene.

Applications Notes

Immunocytochemistry: Recommended dilution: 1-4 μg/ml. Western blotting: Recommended dilution: 1-2 μg/ml. Immunohistochemistry (paraffin sections) : Recommended dilution: 1-2 μg/ml. Immunoprecipitation: Recommended dilution: 1-2 μg / 100-500 μg of protein per 1 mL lysate.

Isotype

Mouse IgG1

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