IRF6 polyclonal, anti-human

Background:
This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. This protein is involved in palate formation.

Other Names:
Interferon regulatory factor 6, IRF-6, IRF6

Antigen Types:
Synthetic Peptide

Gene Name:
IRF6
Gene ID:
3664
Primary Accession: O14896
Other Accession: NP_006138;3664;54139 (mouse);