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.
Formulation
0.5mg/ml if reconstituted with 0.2ml sterile DI water
Host
Rabbit
Immunogen Region
Amino acids FYQVMERVQQAVWEHQR from the human protein were used as the immunogen for the Arylsulfatase L antibody.
Isotype
IgG
Predicted Reactivity
Human, Monkey
Reactivity
Monkey, Human
Recombinant
No
Antigen
Arylsulfatase L
Uniprot
P51690
Buffer
Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide
Format
Antigen affinity purified
Purification
Affinity purified
Storage
After reconstitution, the Arylsulfatase L antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.