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SP110 antibody [N1N2], N-term

Research Use Only
GTX114489
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetSP110
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Overview

  • Supplier
    GeneTex
  • Product Name
    SP110 antibody [N1N2], N-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.82 mg/ml
  • Conjugate
    Unconjugated
  • Formulation
    Liquid
  • Gene ID3431
  • Target name
    SP110
  • Target description
    SP110 nuclear body protein
  • Target synonyms
    IFI41; IFI75; interferon-induced protein 41, 30kD; interferon-induced protein 41/75; interferon-induced protein 75, 52kD; IPR1; phosphoprotein 41; phosphoprotein 75; sp110 nuclear body protein; speckled 110 kDa; transcriptional coactivator Sp110; VODI
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9HB58
  • Protein Name
    Sp110 nuclear body protein
  • Scientific Description
    The nuclear body is a multiprotein complex that may have a role in the regulation of gene transcription. This gene is a member of the SP100/SP140 family of nuclear body proteins and encodes a leukocyte-specific nuclear body component. The protein can function as an activator of gene transcription and may serve as a nuclear hormone receptor coactivator. In addition, it has been suggested that the protein may play a role in ribosome biogenesis and in the induction of myeloid cell differentiation. Alternative splicing has been observed for this gene and three transcript variants, encoding distinct isoforms, have been identified. [provided by RefSeq]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Identification of up- and down-regulated proteins in doxorubicin-resistant uterine cancer cells: reticulocalbin-1 plays a key role in the development of doxorubicin-associated resistance. May EW et al., 2014 Dec, Pharmacol Res
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