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ALG3 encodes a member of the ALG3 family. De plus, nous expédions Asparagine-Linked Glycosylation 3, alpha-1,3 Mannosyltransferase Homolog (S. Cerevisiae) Anticorps (2) et beaucoup plus de produits pour cette protéine.
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Silencing ALG3 or HSF2 inhibited the proliferation, migration, and invasion abilities of MCF-7 cells.
ALG3-CDG is due to an autosomal recessive defect in the ER mannosyl-transferase VI, which is involved in protein N (Montrer NP Protéines)-glycosylation. The enzyme is encoded by the ALG3 gene
a mutation in ALG3 affects splicing and may have a role in development of congenital disorder of glycosylation type Id [case report]
This gene encodes a member of the ALG3 family. The encoded protein 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. Multiple transcript variants encoding different isoforms have been found for this gene.
, asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)
, asparagine-linked glycosylation 3 homolog (yeast, 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
, dol-P-Man dependent alpha(1-3)-mannosyltransferase
, dol-P-Man dependent alpha-1,3- mannosyltransferase
, dol-P-Man-dependent alpha(1-3)-mannosyltransferase
, dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase
, dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase
, dolichyl-phosphate-mannose--glycolipid alpha-mannosyltransferase
, alpha-1,3-mannosyltransferase ALG3
, not56-like protein