S5A1 Polyclonal Antibody, 100ul Serum cap-free design offers flexibility for

cap-free design offers flexibility for your boldest lab experiments

Mutations in FKRP have been associated with congenital muscular dystrophy

Among its related pathways are Endocytosis and Notch Signaling Pathways

Defects in this gene are a cause of mental retardation autosomal dominant type 5 (MRD5)

PTAFR (platelet activating factor receptor) encodes a seven-transmembrane G-protein-coupled receptor for platelet-activating factor (PAF) that localizes to lipid rafts and/or caveolae in the cell membrane

S5A1 Polyclonal Antibody, 100ul Serum cap-free design offers flexibility forSteroid 5 alpha reductase (EC 1. 3. 99. 5) catalyzes the conversion of testosterone into the more potent androgen, dihydrotestosterone (DHT). Also see SRD5A2 (MIM 607306).