GFAP(GA-5 + ASTRO/789), 0.2mg/mL, Clone: [GA-5 ASTRO/789], Mouse, Monoclonal

Catalog Number: BOT-BNUB0898-500
Article Name: GFAP(GA-5 + ASTRO/789), 0.2mg/mL, Clone: [GA-5 ASTRO/789], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB0898-500
Supplier Catalog Number: BNUB0898-500
Alternative Catalog Number: BOT-BNUB0898-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: IHC, WB
Species Reactivity: Bovine, Gallus, Human, Mouse, Porcine, Rabbit, Rat
Immunogen: GFAP isolated from pig spinal cord (GA-5), Recombinant GFAP protein (ASTRO/789)
Alternative Names: Astrocyte or Intermediate Filament Protein, Glial Fibrillary Acidic Protein (GFAP)
This MAb recognizes a protein of ~50 kDa which is identified as Glial Fibrillary Acidic Protein (GFAP). It shows no cross-reaction with other intermediate filament proteins. GFAP is specifically found in astroglia. GFAP is a very popular marker for localizing benign astrocyte and neoplastic cells of glial origin in the central nervous system. Antibody to GFAP is useful in differentiating primary gliomas from metastatic lesions in the brain and for documenting astrocytic differentiation in tumors outside the CNS.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [GA-5 ASTRO/789]
Molecular Weight: ~50 kDa
UniProt: P14136
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 1-2 ug/mL|Immunohistology formalin-fixed 0.25-0.5 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Western blotting 0.5-1 ug/mL|Optimal dilution for a specific application should be determined by user