ALG1 Antikörper

Produktnummer ABIN2459287

Produktdetails anti-ALG1 Antikörper

Target: ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALG1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ALG1.

Anwendungsinformationen

Applikationshinweise: ALG1 antibody can be used for detection of ALG1 by ELISA at 1:62500. ALG1 antibody can be used for detection of ALG1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Konzentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: For short periods of storage (days) store at 4 °C. For longer periods of storage, store ALG1 antibody at -20 °C.

Details zu ALG1

Target: ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))

Andere Bezeichnung: ALG1 (ALG1 Produkte)

Synonyme: CDG1K antikoerper, HMAT1 antikoerper, HMT-1 antikoerper, HMT1 antikoerper, MT-1 antikoerper, Mat-1 antikoerper, hMat-1 antikoerper, zgc:66221 antikoerper, wu:fi34b12 antikoerper, alg1 antikoerper, hmat1 antikoerper, hmt1 antikoerper, ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase antikoerper, asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase) antikoerper, Beta-mannosyltransferase antikoerper, ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog antikoerper, ALG1 antikoerper, Alg1 antikoerper, alg1 antikoerper, alg1.L antikoerper

Hintergrund: ALG1 catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K).The biosynthesis of lipid-linked oligosaccharides is highly conserved among eukaryotes and is catalyzed by 14 glycosyltransferases in an ordered stepwise manner. Mannosyltransferase I (MT I) catalyzes the first mannosylation step in this process.

Molekulargewicht: 52 kDa

Gen-ID: 56052

NCBI Accession: NP_061982

UniProt: Q9BT22