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, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NAGLU-20-RE | 20 (40 μL) | 200 μL |  |
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| NAGLU-20-OR | 20 (40 μL) | 200 μL |  |
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| NAGLU-20-GO | 20 (40 μL) | 200 μL |  |
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| NAGLU-20-GR | 20 (40 μL) | 200 μL |  |
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| NAGLU-20-AQ | 20 (40 μL) | 200 μL |  |
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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, Jul 2008]
Gene Symbol : NAGLU
Gene Name : N-acetyl-alpha-glucosaminidase
Chromosome : CHR 17: 425,359,32-425,444,48
Locus : 17q21.2
Alt. Genes : LRPPRC
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