Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ARSB-20-RE | 20 (40 μL) | 200 μL |  |
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| ARSB-20-OR | 20 (40 μL) | 200 μL |  |
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| ARSB-20-GO | 20 (40 μL) | 200 μL |  |
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| ARSB-20-GR | 20 (40 μL) | 200 μL |  |
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| ARSB-20-AQ | 20 (40 μL) | 200 μL |  |
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Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2016]
Gene Symbol : ARSB
Gene Name : Arylsulfatase B
Chromosome : CHR 5: 789,865,33-787,772,08
Locus : 5q14.1
Alt. Genes : FEM1B
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