Rhodopsin Polyclonal Antibody, 100ul[BT-AP07833] Electronic Pipette The protein encoded by this

The protein encoded by this gene is localized to the cytoplasmic face of the nuclear pore complex where it is required for proper cell cycle progression and nucleocytoplasmic transport

A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2

the complex also influences the Golgi structural integrity

This gene encodes the E1 beta subunit

Rhodopsin Polyclonal Antibody, 100ul[BT-AP07833] Electronic Pipette The protein encoded by thisRetinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X linked recessive disorder. In the autosomal dominant form, which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor specific protein rhodopsin. This is the transmembrane protein which, when