Description |
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. |
Catalog Number |
IW-MA1045 |
Quantity |
9 ml |
Host |
Mouse |
Clone |
GA-8 |
Isotype |
Mouse IgG1 |
Immunogen |
GFAP from pig spinal cord. |
Purity |
Purified by the goat anti-mouse IgG affinity chromatography |
Conjugate |
Unconjugated |
Species Reactivity |
Human, mouse, rat. Not tested in other species. |
Positive Control |
Brain |
Cellular Localization |
Cytoplasmic |
Form |
Ready to use solution in PBS with stabilizer and 0.01% sodium azide. No further dilution needed. Serum blocking step should be omitted. |
Storage |
Store at 2-8 °C. Do not freeze. |
Applications |
IHC-P: Heat induced epitope retrieval is required on formalin fixed paraffin sections. IHC-Tek Epitope Retrieval Solution (IW-1100) is recommended. IHC-Fr: Formalin fixed or acetone fixed frozen sections. ICC: Not tested. |
Limitations |
This product is intended for Research Use Only. Interpretation of the test results is solely the responsibility of the user. |
Precautions |
Users should follow general laboratory precautions when handling this product. Wear personal protective equipment to avoid contact with skin and eyes. |
References |
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. |