ALG11 产品
(Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
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Latest Publications for our ALG11 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).: "Large-scale mapping of human protein-protein interactions by mass spectrometry. ..." in: Molecular systems biology, Vol. 3, pp. 89, (2007) (PubMed).
Synonyms and alternative names related to ALG11
asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase (alg11), ALG11, alpha-1,2-mannosyltransferase (ALG11), ALG11, alpha-1,2-mannosyltransferase L homeolog (alg11.L), ALG11, alpha-1,2-mannosyltransferase (Alg11), asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase) (Alg11), asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase) (alg11), AI849156, AW492253, B230397C21, CDG1P, GT8, RGD1564725, si:dkey-1h24.5, UTP14C, wu:fj04e04Protein level used designations for ALG11
- Asparagine-linked glycosylation protein 11 homolog
- GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
- asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog
- asparagine-linked glycosylation protein 11 homolog
- glycolipid 2-alpha-mannosyltransferase
- GDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase
- asparagine-linked glycosylation 11 homolog (S. cerevisiae, alpha-1,2-mannosyltransferase)
- asparagine-linked glycosylation 11 homolog (yeast, alpha-1,2-mannosyltransferase)
- fj04e04