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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:128,000.
This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.
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: acidic sugar transporter; FLJ22227; FLJ23268; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; hp59; infantile sialic acid storage disorder; membrane glycoprotein HP59; sialic acid storage disease; sodium/sialic acid cotransporter; solute carrier family 17 (acidic sugar transporter), member 5; solute carrier family 17 (anion/sugar transporter), member 5; unnamed protein product; vesicular excitatory amino acid transporter; vesicular H(+)/Aspartate-glutamate cotransporter
基因别名: AST; ISSD; NSD; SD; SIALIN; SIASD; SLD; VEAT
UniProt ID: (Human) Q9NRA2
Entrez Gene ID: (Human) 26503