ZHX3 Polyclonal Antibody, 20ul Cell Function Analysis Alterations in this region have

Alterations in this region have been associated with the Beckwith-Wiedemann syndrome

™ Human IL-6 One-Step ELISA Kit-96 Tests

Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

It is an important effector controlling blood pressure and volume in the cardiovascular system

ZHX3 Polyclonal Antibody, 20ul Cell Function Analysis Alterations in this region haveThis gene encodes a member of the zinc fingers and homeoboxes (ZHX) gene family. The encoded protein contains two C2H2 type zinc fingers and five homeodomains and forms a dimer with itself or with zinc fingers and homeoboxes family member 1. In the nucleus, the dimerized protein interacts with the A subunit of the ubiquitous transcription factor nuclear factor Y and may function as a transcriptional repressor.