ALG3 Antibody

Asparagine-linked glycosylation protein 3 (ALG3) is member of the ALG3 family. ALG3 catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation [taken from NCBI Entrez Gene (Gene ID: 10195)].
ALG3
ALG3, alpha-1,3- mannosyltransferase
Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase
:  asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase) asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog asparagine-linked glycosylation protein 3 homolog carbohydrate deficient glycoprotein syndrome type IV CDG1D CDGS4 CDGS6 D16Ertd36e dolichyl-phosphate-mannose--glycolipid alpha-mannosyltransferase dol-P-Man dependent alpha(1-3)-mannosyltransferase dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase not Not56 NOT56L Not56-like protein More... Less...
Product
Specifications
Ordering Information
Human
WB
between 1 and 50
$229
$99