Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Predicted reactivity: Mouse (86%), Bovine (89%).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Alpha-N-acetylglucosaminidase; alpha-N-acetylglucosaminidase, lysosomal; N-acetyl-alpha-glucosaminidase; N-acetyl-glucosaminidase; N-acetylglucosaminidase, alpha; NAG; testicular tissue protein Li 18
Gene Aliases: CMT2V; MPS-IIIB; MPS3B; NAG; NAGLU; RGD1564228; UFHSD; UFHSD1
UniProt ID: (Human) P54802
Entrez Gene ID: (Human) 4669, (Rat) 360630, (Mouse) 27419
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