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Products:Immunology >> Innate Immunity >> Cytokines >> Interferons
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ab23204 |
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Read our guarantee »Anti-IRF6 antibody
See all IRF6 products (8) ...
Goat polyclonal to IRF6
ELISA, WBmore details
Reacts with
Human
Synthetic peptide: C-TPSMQLPPALPPQ, corresponding to C terminal amino acids 455-467 of Human IRF6(Peptide available as ab232 04.)
C-TPSMQLPPALPPQ
Human Ovary lysate.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 0.5% BSA, Tris-saline. pH 7.3
Concentration information loading...
Immunogen affinity purified
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> Transcription >> Transcription Factors
Stem Cells >> Embryonic Stem Cells >> Cytokines
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> HLH / Leucine Zipper >> Helix-Turn-Helix
Immunology >> Innate Immunity >> Cytokines >> Interferons
Our Abpromise guarantee covers the use of ab10925 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: 1/32000.
WB: Use at a concentration of 0.2 - 1 µg/ml. Detects a band of approximately 60 kDa (predicted molecular weight: 58 kDa) in Human Ovary lysate.
Not tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Probable DNA-binding transcriptional activator. Key determinant of the keratinocyte proliferation-differentiation switch involved in appropriate epidermal development (By similarity). Plays a role in regulating mammary epithelial cell proliferation.
Expressed in normal mammary epithelial cells. Expression is reduced or absent in breast carcinomas.
Defects in IRF6 are a cause of van der Woude syndrome (VWS) [MIM:119300]; also known as lip-pit syndrome (LPS). It is an autosomal dominant developmental disorder characterized by lower lip pits, cleft lip and/or cleft palate. Penetrance is incomplete. Van der Woude and popliteal pterygium syndrome are allelic disorders.
Defects in IRF6 are the cause of popliteal pterygium syndrome (PPS) [MIM:119500]. PPS is an autosomal dominant developmental disorder characterized by cleft lip and/or cleft palate, and skin and genital anomalies. Penetrance is incomplete and expressivity is variable. It shows orofacial phenotypic similarities with van der Woude syndrome. Van der Woude and popliteal pterygium syndrome are allelic disorders.
Genetic variation in IRF6 is associated with non-syndromic orofacial cleft type 6 (OFC6) [MIM:608864]; also called non-syndromic cleft lip with or without cleft palate 6. Non-syndromic orofacial cleft is a common birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum.
Belongs to the IRF family.
Contains 1 IRF tryptophan pentad repeat DNA-binding domain.
Phosphorylated. Phosphorylation status depends on the cell cycle and is a signal for ubiquitination and proteasome-mediated degradation.
Nucleus. Cytoplasm. Translocates to nucleus in response to an activating signal.
Target information above from: UniProt accessionO14896
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ab10925 has not yet been referenced specifically in any publications.
Publishing research using ab10925? Please let us know so that we can cite the reference in this datasheet
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