SRA1 Rabbit Polyclonal Antibody, 50ul Transporters Mutations in this gene cause

Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD)

The products encoded by these genes function in signal transduction pathways

PCR inhibitor-free

In addition to its inhibitory role against most of the known MMPs

The encoded kinase plays a role in cell cycle checkpoint arrest in response to stalled replication forks by phosphorylating Claspin

SRA1 Rabbit Polyclonal Antibody, 50ul Transporters Mutations in this gene causeBoth long non coding and protein coding RNAs are transcribed from this gene and they represent alternatively spliced transcript variants. This gene was initially defined as a non coding RNA which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer. It has now been found that this gene is involved in the regulation of many NR and non NR activities including metabolism adipogenesis and chromatin organization. The