Arylsulfatase F Polyclonal Antibody, 100ul Lentiviral Packaging May mediate homophilic as well

May mediate homophilic as well as heterophilic cell-cell interaction and contribute to signal transduction through its intracellular domain

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

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

The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors

Arylsulfatase F Polyclonal Antibody, 100ul Lentiviral Packaging May mediate homophilic as wellARSF 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.