This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate.
Alpha-N-acetylglucosaminidase; Alpha-N-acetylglucosaminidase 77 kDa form; Alpha-N-acetylglucosaminidase 82 kDa form; alpha-N-acetylglucosaminidase, lysosomal; MPS-IIIB MPS3B NAG UFHSD N-acetyl-alpha-glucosaminidase alpha-N-acetylglucosaminidase; N-acetyl-alpha-glucosaminidase; N-acetyl-glucosaminidase; N-acetylglucosaminidase, alpha; NAG; testicular tissue protein Li 18
Cat # 15716431
100 µL
Cat # 13444637
100 µL
Cat # 16121645
50 uL
Cat # 13402377
100 µL
Cat # 16131645
100 ug
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