The Anti-GFAP 68-377 Recombinant Monoclonal Antibody (HDAB0206) is a highly specific antibody designed for research involving glial fibrillary acidic protein (GFAP), a key intermediate filament protein found in astrocytes. This antibody, produced using recombinant monoclonal technology, is highly sensitive and specific for detecting GFAP in various samples.GFAP is a well-known marker for astrocytes, the most abundant cell type in the central nervous system. It plays a crucial role in maintaining the structure and function of astrocytes, as well as in responding to brain injuries and diseases. The Anti-GFAP 68-377 antibody is ideal for studying the expression and localization of GFAP in both normal and pathological conditions, making it a valuable tool for neuroscience and neurology research.
With its high sensitivity and specificity, the Anti-GFAP 68-377 Recombinant Monoclonal Antibody (HDAB0206) is an essential reagent for researchers investigating neurodegenerative diseases, brain injuries, and other conditions affecting astrocytes and the central nervous system. Its reliable performance in various applications, including immunohistochemistry and western blotting, ensures accurate and reproducible results for your research needs.
SKU:
HDAB0206
Size:
100 µg
Clonality:
Monoclonal
Clone:
DM216
Synonyms:
ALXDRD
Applications:
ELISA
Recommended Dilution:
ELISA 1:5000-10000
Host Species:
Rabbit
Isotype:
Rabbit IgG
Reactivity:
Human
Purification Method:
Purified from cell culture supernatant by affinity chromatography
Formulation:
Powder
Buffer:
1XPBS
Storage:
Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing).Lyophilized antibodies are shipped at ambient temperature.
Usage:
Research use only
Background:
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It 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 results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
