GFAP Mouse Monoclonal Antibody [Clone ID: LBI13C9]
Product Specifications
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]
Synonyms
ALXDRD
Gene Name
Homo sapiens glial fibrillary acidic protein (GFAP), transcript variant 1, mRNA.
Gene ID
2670
UniProt
P14136
Conjugation
Unconjugated
Dilution
ELISA 1:5000-10000
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
ES Cell Differentiation/IPS
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
GFAP
Overview
Carrier-free (BSA/glycerol-free) GFAP mouse monoclonal antibody, clone LBI13C9
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=2670
Uniprot URL
https://www.uniprot.org/uniprot/P14136
Curated Selection
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