RevMab

anti-GFAP, Rabbit Monoclonal (RM246)

CHF 459.00
In stock
REV-31-1127-00-R100100 µlCHF 459.00
More Information
Product Details
Synonyms Glial Fibrillary Acidic Protein
Product Type Recombinant Antibody
Properties
Clone RM246
Isotype Rabbit IgG
Source/Host Rabbit
Immunogen/Antigen A peptide corresponding to the N-terminus of human GFAP.
Application

Immunohistochemistry (IHC): 1:200-1:500 dilution
Western Blot (WB): 1:1000-1:3000 dilution

Crossreactivity Human
Mouse
Specificity

This antibody reacts to human and mouse GFAP (Glial fibrillary acidic protein).

Purity Protein A purified.
Purity Detail Protein A affinity purified from an animal origin-free culture supernatant.
Concentration N/A
Formulation Liquid. 50% Glycerol/PBS with 1% BSA and 0.09% sodium azide.
Isotype Negative Control

Rabbit IgG

Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

Accession Number P14136
Declaration Manufactured by RevMab Biosciences.
Shipping and Handling
Shipping BLUE ICE
Long Term Storage -20°C
Handling Advice Avoid freeze/thaw cycles.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF
Description

GFAP (Glial fibrillary acidic protein) is a member of the class III intermediate filament protein family. GFAP is expressed in the central nervous system in astrocyte cells. It is involved in many important CNS processes, including cell communication and the functioning of the blood brain barrier. GFAP is heavily and specifically expressed in astrocytes and certain astroglia of the central nervous system, in satellite cells of peripheral ganglia, and in non-myelinating Schwann cells of peripheral nerves. In addition, neural stem cells strongly express GFAP. GFAP is closely related to the other three non-epithelial type III IF family members, vimentin, desmin and peripherin, which are all involved in the structure and function of the cell’s cytoskeleton. GFAP is thought to help to maintain astrocyte mechanical strength as well as the shape of cells. GFAP is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing of the GFAP gene results in multiple transcript variants encoding distinct isoforms. In addition, many types of brain tumor, presumably derived from astrocytic cells, heavily express GFAP.

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