GFAP antibody

Catalog No. ABIN7204372

This anti-GFAP antibody is a Mouse Monoclonal antibody detecting GFAP in WB, IF and IHC (p). Suitable for Rat and Mouse.

Quick Overview for GFAP antibody (ABIN7204372)

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

Reactivity: Rat, Mouse

Host: Mouse

Clonality: Monoclonal

Conjugate: This GFAP antibody is un-conjugated

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

Product Details anti-GFAP Antibody

Purpose: GFAP Monoclonal Antibody

Specificity: The antibody detects endogenous GFAP proteins.

Purification: The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen

Immunogen: Synthetic Peptide

Isotype: IgG1

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:2000-1:5000), IF (1:100-1:200), IHC-P (1:50-1:300).

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for GFAP

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

Alternative Name: GFAP

Background: Mouse Anti-GFAP Monoclonal Antibody,GFAP, Glial fibrillary acidic protein, GFAP,GFAP encodes glial fibrillary acidic protein, 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 GFAP cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.,Glial fibrillary acidic protein

Gene ID: 2670

UniProt: P14136