Synthetic peptide within Human GLB1L aa 122-150 (N terminal) conjugated to Keyhole Limpet Haemocyanin (KLH). The exact sequence is proprietary.Database link: Q6UWU2
GLB1L (galactosidase, beta 1-like) is a protein-coding gene. Diseases associated with GLB1L include gangliosidosis, and leber congenital amaurosis, and among its related super-pathways are Metabolism of carbohydrates and Sphingolipid metabolism. GO annotations related to this gene include cation binding and beta-galactosidase activity. An important paralog of this gene is GLB1L3.
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