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A genome-wide high-throughput siRNA screen revealed that KIR2DL4 (zeige KIR2DL4 Proteine) recognition of cell-surface ligand(s) is directly regulated by heparan sulfate glucosamine 3-O-sulfotransferase 3B1 (HS3ST3B1).
Genetic variants of HS3ST3A1 (zeige HS3ST3A1 Proteine) and HS3ST3B1 are associated with Plasmodium falciparum parasitaemia.
the results from this study unveiled a distinct function for 3-OST (zeige HS3ST1 Proteine)-3B1 as an Epithelial-mesenchymal transition inducer in cancer and provided a link between histone modification and Epithelial-mesenchymal transition modulation.
HS3ST3B1 showed potent inhibitory effect on HBV replication.
findings indicate that HS3ST3B1 gene behaves as a primary response gene, suggesting that it may play an important role in making 3-O-sulfated (zeige SULF1 Proteine) HS with specific functions in the regulation of inflammatory and immune responses.
Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. The enzyme encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. It is a type II integral membrane protein and possesses heparan sulfate glucosaminyl 3-O-sulfotransferase activity. The sulfotransferase domain of this enzyme is highly similar to the same domain of heparan sulfate D-glucosaminyl 3-O-sulfotransferase 3A1, and these two enzymes sulfate an identical disaccharide. This gene is widely expressed, with the most abundant expression in liver and placenta.
, heparan sulfate 3-O-sulfotransferase 3B1
, heparan sulfate D-glucosaminyl 3-O-sulfotransferase 3B1
, heparan sulfate glucosamine 3-O-sulfotransferase 3B1
, D-glycosaminyl 3-O-sulfotransferase-3B