GFAP Mouse Monoclonal Antibody [Kloon ID: LBI13C9]

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]

Carrier-free (BSA/glycerol-free) GFAP mouse monoclonal antibody, clone LBI13C9

ALXDRD

Homo sapiens glial fibrillary acidic protein (GFAP), transcript variant 1, mRNA.

2670

P14136

Unconjugated

ELISA 1:5000-10000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

ES Cell Differentiation/IPS

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.

GFAP

https://www.ncbi.nlm.nih.gov/gene/?term=2670

https://www.uniprot.org/uniprot/P14136