Product overview:

Carrier-free (BSA/glycerol-free) GFAP mouse monoclonal antibody, clone LBI2F2

Field of research:

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Summary:

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]

Alternative names:

ALXDRD

Species reactivity:

Human

Host:

Mouse

Target:

GFAP

Isotype:

IgG1

Immunogen:

Full length human recombinant protein of human GFAP (NP_002046) produced in E.coli.

Clone:

LBI2F2

Conjugation:

Unconjugated

Gene name:

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

Symbol:

GFAP

Pathway:

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Function:

ES Cell Differentiation/IPS

Purification:

Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Concentration:

Form:

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

Applications & dilution:

ELISA 1:5000-10000

Storage buffer:

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

Storage:

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.

More info:

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Orders:

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