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JunB antibody

GTX79258
GeneTex
TargetJunb
Product group Antibodies
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Overview

  • Supplier
    GeneTex
  • Product Name
    JunB antibody - Orthogonal Validated
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 10 microg/ml. ICC/IF: 2microg/ml. FACS: 3-5 microg/106 cells. ChIP assay: 1-3 microl. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Formulation
    Liquid
  • Gene ID16477
  • Target name
    Junb
  • Target description
    jun B proto-oncogene
  • Target synonyms
    Jun-B oncogene; myD21; transcription factor jun-B
  • Protein IDP09450
  • Protein Name
    Transcription factor jun-B
  • Scientific Description
    Cellular oncogenes, or proto-oncogenes, play pivotal roles in cellular communication pathways that regulate normal growth, development and differentiation. The cellular oncogene families fos and jun encode nuclear proteins that can function as transcription factors. The fos family of nuclear oncogenes encode cFos, FosB, (fos-related antigen) Fra1, and Fra2. Fos and Jun dimerize to form Activator Protein-1 (AP-1), a transcriptional factor that binds to the 12-O-tetradecanoylphorbol 13-acetate (TPA) response element (TRE) of several cellular and viral genes including human collagenase, metallothionein IIa, stromelysin, interleukin 2, SV40 and polyoma. Fos and Jun contain the leucine-zipper motif that allows for dimerization and an adjacent basic domain required for biological activity. The functionally active form of Fos is in a heterodimer with a member of the Jun family. While Jun family members can form functional homodimers, studies indicate that Fos family members do not self-associate and therefore do not bind DNA on their own. The various dimers differ in their ability to transactivate AP-1 dependent genes.
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Enhanced JunD/RSK3 signalling due to loss of BRD4/FOXD3/miR-548d-3p axis determines BET inhibition resistance. Tai F et al., 2020 Jan 14, Nat Commun
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