Recombinant Anti-GFAP Antibody, Rabbit Monoclonal sinobiological 100140-R012

$171.00
In stock
SKU
100140-R012
Catalog No.SizePrice (USD)
100140-R012-5050 µL$177.58
100140-R012-100100 µL$340.51

General Information

Product nameRecombinant Anti-GFAP Antibody, Rabbit Monoclonal
Validated applicationsWB (FAQ Protocol)
Species reactivityReacts with: Human
SpecificityHuman GFAP
ImmunogenA synthetic peptide corresponding to the center region of the human GFAP
PreparationThis antibody was obtained from a rabbit immunized with a synthetic peptide corresponding to the center region of the human GFAP.
SourceMonoclonal Rabbit IgG Clone #012
PurificationProtein A
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-ALXDRD Antibody; Anti-FLJ45472 Antibody

Image / Experimental Information

Image 1 DescriptionAnti-GFAP rabbit monoclonal antibody at 1:500 dilution Lane A: Mouse brain tissue lysate Lysates/proteins at 30 μg per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:50 kDa Observed band size:45 kDa
Image 1 Alt TextHuman GFAP Western blot (WB) 6433
Image 1 URLSource image

Background Information

Full Nameglial fibrillary acidic protein
DescriptionGFAP is a cell-specific marker which belongs to the intermediate filament family. It can distinguish astrocytes from other glial cells during development. GFAP is expressed in cells lacking fibronectin. It is a type III intermediate filaments protein which contains three domains: the head, rod and tail domains. GFAP functions in many important entral nervous system (CNS) processes, including cell communication and the functioning of the blood brain barrier. Improper GFAP regulation can cause multiple disorders. Defects in GFAP is related to Alexander disease which 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.
Research Areas
  • Neuroinflammation
References
  1. Buniatian G, et al., 1998, Biology of the cell. 90(1): 53-61.
  2. Chen YS, et al., 2011, Experimental Cell Research. 317(16): 2252-66.
  3. Isaacs A, et al., 1998, Genomics. 51(1): 152-4.

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