GFAP Mouse Monoclonal Antibody [Clone ID: LBI4D11]
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.
Synonyms
ALXDRD
Gene Name
Homo sapiens glial fibrillary acidic protein (GFAP), transcript variant 1, mRNA.
Gene ID
2670
UniProt
P14136
Conjugation
Unconjugated
Dilution
WB 1:2000, IHC: 1:50-1:150
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 LBI4D11
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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