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Icam 1 cd54 pe

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ICAM-1 (CD54)-PE is a fluorescently labeled antibody that binds to the Intercellular Adhesion Molecule 1 (ICAM-1) cell surface protein, also known as CD54. ICAM-1 is involved in cell-cell adhesion and plays a role in various immunological processes.

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Lab products found in correlation

Cea cd66 fitc, by BD (2 mentions) Muc1 cd227 fitc, by BD (2 mentions) Facscalibur flow cytometer, by BD (1 mentions) Cellquest software, by BD (1 mentions) Isotype matched controls, by BD (1 mentions) Facscalibur, by BD (1 mentions) Cd44 fitc, by BD (1 mentions) Facsverse, by BD (1 mentions) Cd137l 4 1bbl pe, by BioLegend (1 mentions) Cd252 ox40l pe, by BioLegend (1 mentions) Pd l1 cd274 pe, by BioLegend (1 mentions) Ctla 4 cd152 pe, by BioLegend (1 mentions) Live dead fixable violet dead stain kit, by Thermo Fisher Scientific (1 mentions) Cd24 percp cy5, by BD (1 mentions) Hla abc pe cy7, by BD (1 mentions)

Spelling variants of this product

ICAM-1 (18 citations) CD54-PE (13 citations) ICAM-1 (CD54) (6 citations) Anti-CD54 (ICAM-1)-PE (4 citations) PE-ICAM-1 (2 citations)

2 protocols using icam 1 cd54 pe

1

Characterization of Tumor Cell Surface and Intracellular Antigens

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Cell-surface and intracytoplasmic staining was performed as previously described [47 (link)]. Surface staining of tumor cells was performed using the primary labeled monoclonal antibodies HLA-A2-FITC, ICAM-1 (CD54)-PE, CEA (CD66)-FITC, MUC1 (CD227)-FITC, and the appropriate isotype-matched controls (BD Biosciences). For intracellular analysis of antigen processing machinery (APM) components, mouse IgG1 (MK2-23) isotype control, LMP2 (SY-1)-, LMP7 (HB2)-, TAP-1 (NOB1), calnexin (TO-5)-, β2-microglobulin (L368), and tapasin (TO-3)-specific monoclonal antibodies were developed and characterized as described [48 (link)-50 (link)]. Cellular fluorescence of 3×104 cells was examined on a FACSCalibur flow cytometer using CellQuest software (BD Biosciences). Proteins were scored as markedly upregulated if confirmed statistically and if detection levels and/or mean fluorescence intensity (MFI) increased ≥ 25% following treatment and were not observed in control cells vs. isotype controls.
Gameiro S.R., Malamas A.S., Tsang K.Y., Ferrone S, & Hodge J.W. (2016). Inhibitors of histone deacetylase 1 reverse the immune evasion phenotype to enhance T-cell mediated lysis of prostate and breast carcinoma cells. Oncotarget, 7(7), 7390-7402.
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2

Flow Cytometry Analysis of Irradiated Tumor Cells

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At 96 h post-irradiation, tumor cells were examined by flow cytometry, as previously described [13 (link)]. Cells were examined on FACSCalibur or FACSVerse cytometers, using the monoclonal antibodies targeting HLA-ABC-FITC, HLA-ABC-PE-Cy7, ICAM-1 (CD54)-PE, CEA (CD66)-FITC, MUC-1 (CD227)-FITC, CD24-PerCP-Cy5.5, CD44-FITC, and the appropriate isotype-matched controls (BD Biosciences, San Jose, CA). The monoclonal antibodies targeting CD70-FITC, CD275 (ICOSL)-PE, CD137L (4-1BBL)-PE, CD252 (OX40L)-PE, PD-L1 (CD274)-PE, CTLA-4 (CD152)-PE, and CD227 (MUC-1)-PE were obtained from BioLegend (San Diego, CA). Antibodies targeting CD133-APC (Miltenyi Biotec, San Diego, CA) and calreticulin-PE (R&D Systems, Minneapolis, MN) were also used. Isotype control staining was < 5% for all samples analyzed. Viability was examined using LIVE/DEAD Fixable Violet Dead Stain Kit (Thermo Fisher Scientific, Rockville, MD). Cell surface expression was evaluated on live cells gated by FSC/SSC and LIVE/DEAD staining.
Gameiro S.R., Malamas A.S., Bernstein M.B., Tsang K.Y., Vassantachart A., Sahoo N., Tailor R., Pidikiti R., Guha C.P., Hahn S.M., Krishnan S, & Hodge J.W. (2016). Tumor Cells Surviving Exposure to Proton or Photon Radiation Share a Common Immunogenic Modulation Signature, Rendering Them More Sensitive to T Cell-Mediated Killing. International journal of radiation oncology, biology, physics, 95(1), 120-130.
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