Rhodopsin Polyclonal Antibody, 100ul[BT-AP07833] Electronic Pipette The frame handle supports aseptic

The frame handle supports aseptic operation

This protein is proposed to be involved in specific calcium-dependent signal transduction pathways and its regulatory effect on cytoskeletal components may modulate various neutrophil activities

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

Hypomethylation at this gene may be associated with lung cancer in human patients

Rhodopsin Polyclonal Antibody, 100ul[BT-AP07833] Electronic Pipette The frame handle supports asepticRetinitis 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