GFOD2 Antikörper (AA 301-385) (FITC)

Produktnummer ABIN1398896

Der Kaninchen Polyklonal Anti-GFOD2-Antikörper wurde für WB, IF (cc) und IF (p) validiert. Er ist geeignet, GFOD2 in Proben von Human zu detektieren.

Kurzübersicht für GFOD2 Antikörper (AA 301-385) (FITC) (ABIN1398896)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GFOD2 Antikörper ist konjugiert mit FITC

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

Produktdetails anti-GFOD2 Antikörper (FITC)

Bindungsspezifität: AA 301-385

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GFOD2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

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

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu GFOD2

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

Andere Bezeichnung: GFOD2

Hintergrund:

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.

Gen-ID: 81577