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. The encoded protein may be a transcriptional activator. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. Mutations in this gene are also associated with non-syndromic orofacial cleft type 6. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2011]
Inmunógeno
A synthetic peptide corresponding to a sequence within amino acids 368-467 of human IRF6 (O14896).
PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3.
Aplicación
WB, IF/ICC, IP
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 1
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Certificados de análisis (COA)
Lot/Batch Number
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