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This antibody is predicted to react with non-human primate based on sequence homology.
This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Cerebroside sulfate activator protein; Ganglioside GM2 activator; GM2-AP; SAP-3; shingolipid activator protein 3; Sphingolipid activator protein 3
Gene Aliases: AA408702; AW215435; GM2-AP; GM2A; SAP-3
UniProt ID: (Human) P17900, (Mouse) Q60648
Entrez Gene ID: (Human) 2760, (Mouse) 14667
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