NR2C1 Polyclonal Antibody, 20ul Stepper The human genome contains five

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

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

Multiple alternatively spliced transcript variants of CDC25C have been described

Two specifications are available: 145 mm and 230 mm

q12) with the pleiomorphic adenoma gene 1

NR2C1 Polyclonal Antibody, 20ul Stepper The human genome contains fiveThis 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.