NR2C1 Polyclonal Antibody, 20ul Stepper Other possible variants have been

Other possible variants have been detected| but their full-length nature has not been determined

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

The human genome contains five CD1 family genes organized in a cluster on chromosome 1

and may play a role in regulating the actin cytoskeleton

Stimulates uterine epithelial cell proliferation

NR2C1 Polyclonal Antibody, 20ul Stepper Other possible variants have beenThis gene encodes a nuclear hormone receptor characterized by a highly conserved DNA binding domain (DBD), a variable hinge region, and a carboxy terminal ligand binding domain (LBD) that is typical for all members of the steroid thyroid hormone receptor superfamily. This protein also belongs to a large family of ligand inducible transcription factors that regulate gene expression by binding to specific DNA sequences within promoters of target genes.