Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
MOGS encodes the first enzyme in the N-linked oligosaccharide processing pathway. Additionally we are shipping Mannosyl-Oligosaccharide Glucosidase Proteins (4) and many more products for this protein.
Showing 10 out of 61 products:
Human Polyclonal MOGS Primary Antibody for EIA, WB - ABIN357670
Völker, De Praeter, Hardt, Breuer, Kalz-Füller, Van Coster, Bause: Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb). in Glycobiology 2002
Show all 3 references for ABIN357670
Human Polyclonal MOGS Primary Antibody for EIA, WB - ABIN357669
De Praeter CM, Gerwig, Bause, Nuytinck, Vliegenthart, Breuer, Kamerling, Espeel, Martin, De Paepe AM, Chan, Dacremont, Van Coster RN: A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency. in American journal of human genetics 2001
Show all 3 references for ABIN357669
Cow (Bovine) Polyclonal MOGS Primary Antibody for WB - ABIN2782707
Hardt, Kalz-Fuller, Aparicio, Volker, Bause: (Arg)3 within the N-terminal domain of glucosidase I contains ER targeting information but is not required absolutely for ER localization. in Glycobiology 2003
A shortened immunoglobulin half-life was determined to be the mechanism underlying the hypogammaglobulinemia in congenital disorder of glycosylation type IIb (CDG-IIb).
Perturbation of free oligosaccharide trafficking in endoplasmic reticulum glucosidase I-deficient and castanospermine-treated cells.
MafF/NFE2 hetrodimers act as weak transcriptional activators, and, in particular, are able to stimulate activity of the GCS1 promoter.
This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene.
, Mannosyl oligosaccharide glucosidase
, mannosyl oligosaccharide glucosidase
, glycoprotein-processing glucosidase I
, glucosidase I
, processing A-glucosidase I
, glucosidase 1