NR1D2 Polyclonal Antibody, 50ul In vitro Assessment interaction with cofactor C then

interaction with cofactor C then causes the release of tubulin polypeptides that are committed to the native state

that is involved in transcription initiation and DNA repair

Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease

Activated by phosphorylation on Thr-211 by STK11 in complex with STE20-related adapter-alpha (STRAD alpha) pseudo kinase and CAB39

This member is BCL7B

NR1D2 Polyclonal Antibody, 50ul In vitro Assessment interaction with cofactor C thenThis gene encodes a member of the nuclear hormone receptor family, specifically the NR1 subfamily of receptors. The encoded protein functions as a transcriptional repressor and may play a role in circadian rhythms and carbohydrate and lipid metabolism. Alternatively spliced transcript variants have been described.