IRF6 is 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.
The function of IRF6 is related to the formation of connective tissue, for example that of the palate.
This gene encodes a member of the interferon regulatory transcription factor (IRF) family.
A mutation of the IRF6 gene can lead to van der Woude syndrome or the related popliteal pterygium syndrome.
These disorders are caused by mutations in the IRF6 gene and some of the phenotypic heterogeneity is due to different types of IRF6 mutations.One explanation for this phenotypic variation between syndromes is based on a differential impact on the structure of the dimerized mutant proteins.
Applications:Suitable for use in ELISA, Western Blot, Immunohistochemistry, Immunocytochemistry.
Other applications not tested.
Recommended Dilution:ELISA: 1:100-5000Western Blot: 1:50-400 Immunohistochemistry (frozen): 1:50-500 Immunohistochemistry (paraffin): 1:10-100Immunocytochemistry: 1:50-500 Optimal dilutions to be determined by the researcher.