GFAP antibody

Catalog No. ABIN659067

This anti-GFAP antibody is a Mouse Monoclonal antibody detecting GFAP in WB, IF and IHC (p). Suitable for Human. This Primary Antibody has been cited in 1 publication.

Quick Overview for GFAP antibody (ABIN659067)

Target: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This GFAP antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: 183CT3-1-5

Product Details anti-GFAP Antibody

Purification: This antibody is purified through a protein G column, followed by dialysis against PBS.

Immunogen: This GFAP monoclonal antibody is generated from mouse immunized with GFAP recombinant protein.

Isotype: IgG2b kappa

Application Details

Application Notes: IF: 1:10~50. WB: 1:4000. WB: 1:100~500. IHC-P-Leica: 1:1000. IHC: 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

References for anti-GFAP antibody (ABIN659067)

Bajpai, Kerosuo, Tseropoulos, Cummings, Wang, Lei, Liu, Liu, Popescu, Bronner, Andreadis: "Reprogramming Postnatal Human Epidermal Keratinocytes Toward Functional Neural Crest Fates." in: Stem cells (Dayton, Ohio), Vol. 35, Issue 5, pp. 1402-1415, (2018) (PubMed).

Target Details for GFAP

Target: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Alternative Name: GFAP

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.

Molecular Weight: 49880

Gene ID: 2670

NCBI Accession: NP_001124491, NP_001229305, NP_002046

UniProt: P14136