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- Tel: 858.663.9055
- Email: info@nsjbio.com
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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
Optimal dilution of the Arylsulfatase B antibody should be determined by the researcher.
Amino acids KTLWLFDINQDPEERHD from the mouse protein were used as the immunogen for the Arylsulfatase B antibody.
After reconstitution, the Arylsulfatase B antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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