- Tel: 858.663.9055
Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene. It is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.
Optimal dilution of the Arylsulfatase L antibody should be determined by the researcher.
Amino acids FYQVMERVQQAVWEHQR from the human protein were used as the immunogen for the Arylsulfatase L antibody.
After reconstitution, the Arylsulfatase L 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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