IRF6
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.
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- Derivation: Camelid
- Species Reactivity: Human
- Type: Camelid VHH
- Application: ELISA
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- Derivation: Phage display library screening
- Species Reactivity: Mouse, Rat, Human
- Type: IgG
- Application: WB, IHC-P, ICC/IF
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: WB, IF, IHC
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- Derivation: Camelid
- Species Reactivity: Human
- Type: Camelid VHH
- Application: ELISA
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- Derivation: Camelid
- Species Reactivity: Human
- Type: Camelid VHH
- Application: ELISA
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- Species Reactivity: Human
- Type: Mouse IgG2b
- Application: IHC-P
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- Species Reactivity: Human
- Type: IgG
- Application: IP, IF
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: WB, ICC, IF, IHC
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- Species Reactivity: Human
- Type: Llama VHH
- Application: ELISA, Neut, ICC, FC
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For Research Use Only. Not For Clinical Use.