POLR2J1 Polyclonal Antibody, 100ul Cell Dissociation CSNB1 is a rare inherited

CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision| myopia| hyperopia| nystagmus and reduced visual acuity

the gene product lacks carbonic anhydrase activity (i

This protein is also thought to have a role during cell cycle progession

Expression of this gene is downregulated by interleukin 3 (IL3)

The use of alternate polyadenylation sites has been found for this gene

POLR2J1 Polyclonal Antibody, 100ul Cell Dissociation CSNB1 is a rare inheritedPOLR2J (RNA polymerase II subunit J) encodes a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of POLR2J exists as a heterodimer with another polymerase subunit; together they form a core subassembly unit of the polymerase. Two similar genes are located nearby on chromosome 7q22 and a pseudogene is found on chromosome 7p13.