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ICAM1 / CD54 antibody [84H10]

GTX76273
GeneTex
ApplicationsFlow Cytometry, ImmunoPrecipitation, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
Product group Antibodies
ReactivityCanine, Human
TargetICAM1
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Overview

  • Supplier
    GeneTex
  • Product Name
    ICAM1 / CD54 antibody [84H10]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody detects an antigen of human CD54 antibody, clone 84H10 has been reported to block ICAM1 mediated cellular adhesion and block binding of LFA-1 and P. falciparum to ICAM-1.
  • Application Supplier Note
    IHC-Fr: 1/20-1/50. FACS: Neat-1/10. IP: 5microg / 107 cells. Neutralizing/Inhibition: . *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoPrecipitation, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    84H10
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3383
  • Target name
    ICAM1
  • Target description
    intercellular adhesion molecule 1
  • Target synonyms
    BB2; CD54; cell surface glycoprotein P3.58; epididymis secretory sperm binding protein; ICAM-1; intercellular adhesion molecule 1; intercellular adhesion molecule 1 (CD54), human rhinovirus receptor; major group rhinovirus receptor; P3.58
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP05362
  • Protein Name
    Intercellular adhesion molecule 1
  • Scientific Description
    This gene encodes a cell surface glycoprotein which is typically expressed on endothelial cells and cells of the immune system. It binds to integrins of type CD11a / CD18, or CD11b / CD18 and is also exploited by Rhinovirus as a receptor. [provided by RefSeq, Jul 2008]
  • Reactivity
    Canine, Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Novel method to repair articular cartilage by direct reprograming of prechondrogenic mesenchymal stem cells. Chang CY et al., 2021 Nov 15, Eur J Pharmacol
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