Overview
Product nameAREB6 peptideSee all AREB6 proteins and peptides ...
Protein descriptionSynthetic peptide derived from within residues 350 - 450 of Human AREB6.(Note: the amino acid sequence is proprietary)This peptide was used as an immunogen for ab64098 - AREB6 antibody.
Protein length1124 amino acids
Properties
Purity70 - 90% by HPLC
FormLiquid
Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Storage bufferInformation available upon request.
Concentration information loading...
Research Areas
Protein info
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Alternative names
AREB 6BZPDelta crystallin enhancer binding factor 1
DELTA EF1FECD6MGC133261Negative regulator of IL 2Negative regulator of IL2NIL 2 ANIL 2 A zinc finger proteinNIL 2ANIL-2-A zinc finger proteinNIL2APosterior polymorphous corneal dystrophy 3PPCD3Represses interleukin 2 expressionTCF 8TCF-8TCF8Transcription factor 8Transcription factor 8 (represses interleukin 2 expression)ZEBZEB 1ZEB1ZEB1_HUMANZFHEPZFHX 1AZFHX1AZinc finger E box binding homeobox 1Zinc finger E-box-binding homeobox 1Zinc finger homeodomain enhancer binding protein
see all
FunctionInhibits interleukin-2 (IL-2) gene expression. May be responsible for transcriptional repression of the IL-2 gene. Enhances or represses the promoter activity of the ATP1A1 gene depending on the quantity of cDNA and on the cell type. Represses E-cadherin promoter and induces an epithelial-mesenchymal transition (EMT) by recruiting SMARCA4/BRG1. Represses BCL6 transcription in the presence of the corepressor CTBP1. Promotes tumorigenicity by repressing stemness-inhibiting microRNAs.
Tissue specificityColocalizes with SMARCA4/BRG1 in E-cadherin-negative cells from established lines, and stroma of normal colon as well as in de-differentiated epithelial cells at the invasion front of colorectal carcinomas (at protein level). Expressed in heart and skeletal muscle, but not in liver, spleen, or pancreas.
Involvement in diseaseDefects in ZEB1 are the cause of posterior polymorphous corneal dystrophy type 3 (PPCD3) [MIM:609141]. PPCD is a rare disease involving metaplasia and overgrowth of corneal endothelial cells. In patients with PPCD, these cells manifest in an epithelial morphology and gene expression pattern, produce an aberrant basement membrane, and, sometimes, spread over the iris and nearby structures in a way that increases the risk for glaucoma.
Defects in ZEB1 are the cause of corneal dystrophy Fuchs endothelial type 6 (FECD6) [MIM:613270]. It is an ocular disorder caused by loss of endothelium of the central cornea. It is characterized by focal wart-like guttata that arise from Descemet membrane and develop in the central cornea, epithelial blisters, reduced vision and pain. Descemet membrane is thickened by abnormal collagenous deposition.
Sequence similaritiesBelongs to the delta-EF1/ZFH-1 C2H2-type zinc-finger family.
Contains 7 C2H2-type zinc fingers.
Contains 1 homeobox DNA-binding domain.
Cellular localizationNucleus.
References for AREB6 peptide (ab66485)
ab66485
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"