OSB11 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Defects in this gene are

Defects in this gene are a cause of long QT syndrome type 10 (LQT10)

and library packaging

different colors are provided for identification

Mutations in these genes have been associated with White Sponge Nevus

The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea

OSB11 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Defects in this gene areThis gene encodes a member of the oxysterol binding protein (OSBP) family a group of intracellular lipid receptors. Like most members the encoded protein contains an N terminal pleckstrin homology domain and a highly conserved C terminal OSBP like sterol binding domain.