MCM9 Polyclonal Antibody, 20ul Rotator P2RY8 is moderately expressed in

P2RY8 is moderately expressed in undifferentiated HL60 cells

thymus and fetal liver

Transcripts for CD44 undergo complex alternative splicing that results in many functionally distinct isoforms

Mutations in this gene are associated with Mitchell-Riley syndrome| which is characterized by neonatal diabetes with pancreatic hypoplasia| duodenal and jejunal atresia| and gall bladder agenesis

Alternatively spliced transcript variants encoding different isoforms have been found for this CDK1

MCM9 Polyclonal Antibody, 20ul Rotator P2RY8 is moderately expressed inThe protein encoded by this gene is a member of the mini chromosome maintenance (MCM) protein family that are essential for the initiation of eukaryotic genome replication. Binding of this protein to chromatin has been shown to be a pre requisite for recruiting the MCM2 7 helicase to DNA replication origins. This protein also binds, and is a positive regulator of, the chromatin licensing and DNA replication factor 1, CDT1.