NAGLU antibody [N3C1], Internal

GeneTex

NAGLU antibody [N3C1], Internal

9

Research Use Only

1 mg/ml

IgG

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. [provided by RefSeq]

2°C to 8°C,-20°C

12352203