Arylsulfatase F Polyclonal Antibody, 100ul Lentiviral Packaging Certain single-nucleotide polymorphism haplotypes of

Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy

Three different versions of extraskeletal myxoid chondrosarcomas (EMCs) are the result of reciprocal translocations between this gene and other genes

is located on Chromosome 15 and is an inhibitor of calcineurin activity and has a genetic phenotype associated with Parkinson's Disease (OMIM:606988)

Mutations in this gene are a cause of branchiootorenal syndrome type 2

The encoded protein has been shown to interact with neurotrophin receptor

Arylsulfatase F Polyclonal Antibody, 100ul Lentiviral Packaging Certain single-nucleotide polymorphism haplotypes ofARSF is a member of the sulfatase family, and more specifically, the arylsulfatase subfamily. Members of the subfamily share similarity in sequence and splice sites, and are clustered together on chromosome X, suggesting that they are derived from recent gene duplication events. Sulfatases are essential for the correct composition of bone and cartilage matrix. The activity of this protein, unlike that of arylsulfatase E, is not inhibited by warfarin.