GFOD2 anticorps (AA 301-385) (Cy5)

N° du produit ABIN1416762

Cet anticorps anti-GFOD2 est un anticorps Lapin Polyclonal détectant GFOD2 dans WB, IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour GFOD2 anticorps (AA 301-385) (Cy5) (ABIN1416762)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GFOD2 est conjugé à/à la Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-GFOD2 anticorps (Cy5)

Épitope: AA 301-385

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GFOD2

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur GFOD2

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

Autre désignation: GFOD2

Sujet:

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.

ID gène: 81577