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抗人 ST6GALNAC5 抗体对
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抗人 ST6GALNAC5 抗体对

01AB01359

ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 (ST6GALNAC5) is a Golgi type II transmembrane glycosyltransferase enzyme consisting of 316 amino acids with a molecular mass of approximately 36.4 kDa. It catalyzes the transfer of sialic acid to cell surface proteins and is specifically involved in the biosynthesis of ganglioside GD1α from GM1b, predominantly expressed in brain tissue. ST6GALNAC5 modulates cell-cell interactions and influences receptor tyrosine kinases via membrane microdomain formation. Functionally, it plays a role in cell junction regulation, differentiation, and metastasis, particularly in prostate and breast cancers. Overexpression of ST6GALNAC5 promotes cancer cell invasion and proliferation by activating pathways such as MAPK/ERK1/2. Notably, it facilitates breast cancer brain metastasis by enabling cancer cells to cross the blood-brain barrier, while its role may vary depending on cancer context, sometimes inhibiting glioma invasiveness.

Human
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技术参数

靶点基因名
ST6GALNAC5
基因别名
SIAT7E
蛋白别名
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5; ST6GALNAC5
UniProt
Q9BVH7
物种
Human

产品详情

靶点名称
ST6GALNAC5
蛋白名称
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5
蛋白别名
Alpha-N-acetylgalactosaminide alpha-2; 6-sialyltransferase 5; GD1 alpha synthase; GalNAc alpha-2; 6-sialyltransferase V; ST6GalNAc V; ST6GalNAcV; Sialyltransferase 7E; SIAT7-E
靶点基因名
ST6GALNAC5
基因别名
SIAT7E
UniProt
Q9BVH7
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 (ST6GALNAC5) is a Golgi type II transmembrane glycosyltransferase enzyme consisting of 316 amino acids with a molecular mass of approximately 36.4 kDa. It catalyzes the transfer of sialic acid to cell surface proteins and is specifically involved in the biosynthesis of ganglioside GD1α from GM1b, predominantly expressed in brain tissue. ST6GALNAC5 modulates cell-cell interactions and influences receptor tyrosine kinases via membrane microdomain formation. Functionally, it plays a role in cell junction regulation, differentiation, and metastasis, particularly in prostate and breast cancers. Overexpression of ST6GALNAC5 promotes cancer cell invasion and proliferation by activating pathways such as MAPK/ERK1/2. Notably, it facilitates breast cancer brain metastasis by enabling cancer cells to cross the blood-brain barrier, while its role may vary depending on cancer context, sometimes inhibiting glioma invasiveness.