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MOGS encodes the first enzyme in the N-linked oligosaccharide processing pathway. Additionally we are shipping Mannosyl-Oligosaccharide Glucosidase Antibodies (66) and many more products for this protein.
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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