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Antibody detects endogenous levels of total CHST5.
The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD).
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5; Carbohydrate sulfotransferase 5; Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-alpha; GlcNAc6ST-3; GST4-alpha; I-GlcNAc6ST; intestinal GlcNAc-6-sulfotransferase; Intestinal N-acetylglucosamine-6-O-sulfotransferase; MCDC1; N-acetylglucosamine 6-O-sulfotransferase 3
基因别名: CHST5; glcNAc6ST-3; gn6st-3; hIGn6ST; I-GlcNAc-6-ST; I-GlcNAc6ST
UniProt ID: (Human) Q9GZS9
Entrez Gene ID: (Human) 23563