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Invitrogen™ IRF6 Recombinant Rabbit Monoclonal Antibody (23GB6550), Invitrogen™
Description
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.
Specifications
Specifications
| Antigen | IRF6 |
| Applications | Flow Cytometry, Western Blot, Immunocytochemistry |
| Classification | Recombinant Monoclonal |
| Clone | 23GB6550 |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 |
| Gene | Irf6 |
| Gene Accession No. | O14896, P97431 |
| Gene Alias | AI876454; E230028I05Rik; interferon regulatory factor 6; IRF6; IRF-6; irf6 protein; IRF-6; transcription factor; LPS; mirf6; OFC6; PIT; PPS; PPS1; transcriptional factor; VWS; VWS1; zgc:63500 |
| Gene Symbols | Irf6 |
| Show More |
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