SMAL1 Rabbit Polyclonal Antibody, 100ul Serum Caveolin 1 and caveolin 2

Caveolin 1 and caveolin 2 are located next to each other on chromosome 7 and express colocalizing proteins that form a stable hetero-oligomeric complex

Defects in this gene cause X-linked Opitz-Kaveggia syndrome

The multi-pass membrane protein encoded by this gene belongs to the G-protein coupled receptor 3 family and GABA-B receptor subfamily

Beare-Stevenson cutis gyrata syndrome

The primary function of the encoded transmembrane protein is the induction of apoptosis triggered by binding to FAS

SMAL1 Rabbit Polyclonal Antibody, 100ul Serum Caveolin 1 and caveolin 2The protein encoded by this gene is a member of the SWI SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD) an autosomal recessive