GALK2 Antikörper (AA 141-240) (Cy5)

Produktnummer ABIN1704910

Produktdetails anti-GALK2 Antikörper (Cy5)

Target: GALK2 (Galactokinase 2 (GALK2))

Bindungsspezifität: AA 141-240

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GALK2 Antikörper ist konjugiert mit Cy5

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

Kreuzreaktivität: Ratte

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GALK2/Galactokinase 2

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 GALK2

Target: GALK2 (Galactokinase 2 (GALK2))

Andere Bezeichnung: GALK2/Galactokinase 2 (GALK2 Produkte)

Synonyme: GK2 antikoerper, 2810017M24Rik antikoerper, AI327030 antikoerper, Gk2 antikoerper, galk2 antikoerper, MGC52969 antikoerper, MGC89048 antikoerper, GALK2 antikoerper, wu:fb43h07 antikoerper, zgc:101686 antikoerper, galactokinase 2 antikoerper, galactokinase 2 L homeolog antikoerper, GALK2 antikoerper, Galk2 antikoerper, galk2.L antikoerper, galk2 antikoerper

Hintergrund:

Synonyms: GaINAc Kinase, Galactokinase 2, GALK2, GK2, MGC1745, N-acetylgalactosamine kinase, GALK2_HUMAN.

Background: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.

Gen-ID: 2585