OSB11 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification different colors are provided for

different colors are provided for identification

Several transcript variants have been observed for this gene

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

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

Mutations in these genes have been associated with White Sponge Nevus

OSB11 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification different colors are provided forThis 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.