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WB analysis of THP-1 (THP) and HeLa (HL) whole cell lysates using GTX31253 IRAK1 antibody. Working concentration : 1 microg/ml
WB analysis of THP-1 (THP) and HeLa (HL) whole cell lysates using GTX31253 IRAK1 antibody. Working concentration : 1 microg/ml
WB analysis of THP-1 (THP) and HeLa (HL) whole cell lysates using GTX31253 IRAK1 antibody. Working concentration : 1 microg/ml

IRAK1 antibody

GTX31253
GeneTex
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ELISA, ImmunoCytoChemistry
Product group Antibodies
TargetIRAK1
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Overview

  • Supplier
    GeneTex
  • Product Name
    IRAK1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 microg/mL. ICC/IF: 10 microg/mL. IP: 2 - 4 microg. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ELISA, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3654
  • Target name
    IRAK1
  • Target description
    interleukin 1 receptor associated kinase 1
  • Target synonyms
    interleukin-1 receptor-associated kinase 1; IRAK; IRAK-1; pelle; Pelle homolog
  • Host
    Rabbit
  • Isotype
    IgG
  • Scientific Description
    This gene encodes the interleukin-1 receptor-associated kinase 1, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. This gene is partially responsible for IL1-induced upregulation of the transcription factor NF-kappa B. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • MicroRNA-146b-5p Suppresses Pro-Inflammatory Mediator Synthesis via Targeting TRAF6, IRAK1, and RELA in Lipopolysaccharide-Stimulated Human Dental Pulp Cells.
    Read more

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