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WB analysis of COLO cell lysates using GTX86994 RNF144A antibody. The lane on the right is blocked with the synthesized peptide.
WB analysis of COLO cell lysates using GTX86994 RNF144A antibody. The lane on the right is blocked with the synthesized peptide.
WB analysis of COLO cell lysates using GTX86994 RNF144A antibody. The lane on the right is blocked with the synthesized peptide.

RNF144A antibody

GTX86994
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse
TargetRNF144A
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Overview

  • Supplier
    GeneTex
  • Product Name
    RNF144A antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500~1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID9781
  • Target name
    RNF144A
  • Target description
    ring finger protein 144A
  • Target synonyms
    RNF144, UBCE7IP4, UIP4, hUIP4, E3 ubiquitin-protein ligase RNF144A, UbcM4-interacting protein 4, probable E3 ubiquitin-protein ligase RNF144A, ring finger protein 144, ubiquitin conjugating enzyme 7 interacting protein 4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP50876
  • Protein Name
    E3 ubiquitin-protein ligase RNF144A
  • Scientific Description
    The protein encoded by this protein contains a RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. The mouse counterpart of this protein has been shown to interact with Ube2l3/UbcM4, which is an ubiquitin-conjugating enzyme involved in embryonic development. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Wu YH, Hong CW, Wang YC, et al. A novel histone deacetylase inhibitor TMU-35435 enhances etoposide cytotoxicity through the proteasomal degradation of DNA-PKcs in triple-negative breast cancer. Cancer Lett. 2017,400:79-88. doi: 10.1016/j.canlet.2017.04.023
    Read this paper