ALG1 产品
(Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))
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Latest Publications for our ALG1 Products
: "A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).Synonyms and alternative names related to ALG1
ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase (ALG1), asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase) (Alg1), ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase (alg1), ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase (Alg1), Beta-mannosyltransferase (ALG1), ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog (alg1.L), alg1, CDG1K, hMat-1, HMAT1, hmat1, HMT-1, HMT1, hmt1, Mat-1, MT-1, wu:fi34b12, zgc:66221Protein level used designations for ALG1
- GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase
- GDP-mannose-dolichol diphosphochitobiose mannosyltransferase
- asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase)
- asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog
- asparagine-linked glycosylation protein 1 homolog
- beta-1,4 mannosyltransferase
- beta-1,4-mannosyltransferase
- chitobiosyldiphosphodolichol beta-mannosyltransferase
- mannosyltransferase-1
- asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase)
- hypothetical protein
- ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog