Arylsulfatase L Antibody / ARSL

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.

P51690

Rabbit

Amino acids FYQVMERVQQAVWEHQR from the human protein were used as the immunogen for the Arylsulfatase L antibody.

Polyclonal

IgG

WB

Antigen affinity purified

0.5mg/ml if reconstituted with 0.2ml sterile DI water

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.

This Arylsulfatase L antibody is available for research use only.

Primary antibody

https://www.nsjbio.com/tds/arylsulfatase-l-antibody-rq5795