GFOD2 antibody (AA 301-385) (Biotin)

Catalog No. ABIN1398895

This Rabbit Polyclonal antibody specifically detects GFOD2 in WB, ELISA, IHC (p) and IHC (fro). It exhibits reactivity toward Human.

Quick Overview for GFOD2 antibody (AA 301-385) (Biotin) (ABIN1398895)

Target: GFOD2 (Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GFOD2 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-GFOD2 Antibody (Biotin)

Binding Specificity: AA 301-385

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GFOD2

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for GFOD2

Target: GFOD2 (Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2))

Alternative Name: GFOD2

Background:

Synonyms: GFOD2, GFOD2_HUMAN, Glucose fructose oxidoreductase domain containing 2, Glucose fructose oxidoreductase domain containing protein 2, Glucose-fructose oxidoreductase domain-containing protein 2, MGC11335.

Background: GFOD2 is a 385 amino acid secreted protein of the extracellular matrix that belongs to the gfo/idh/mocA family. Existing as two alternatively spliced isoforms, GFOD2 enhances matrix assembly and is encoded by a gene that maps to human chromosome 16q22.1. Chromosome 16 encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Gene ID: 81577