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Iodogen pre coated tubes

Manufactured by PerkinElmer

Iodogen pre-coated tubes are a type of laboratory equipment used for the iodination of proteins. The tubes are pre-coated with a reagent called Iodogen, which facilitates the covalent labeling of proteins with radioactive iodine isotopes. This process is commonly employed in various research applications, such as the study of protein-protein interactions and the preparation of labeled proteins for immunoassays.

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6 protocols using iodogen pre coated tubes

1

Monoclonal Anti-ICAM-1 Binding Assay

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Monoclonal mouse anti-human ICAM-1 (anti-ICAM) was clone R6.5 (American Type Culture Collection; Manassas, VA). Non-specific mouse IgG and secondary goat anti-mouse IgG were from Jackson Immunoresearch (West Grove, PA). Dextranase (Dxase) from Penicillium janthinellum was from Sigma Aldrich (St. Louis, MO). Fluoresbrite® polystyrene latex particles were from Polysciences (Warrington, PA). 125Iodine (125I) and Iodogen pre-coated tubes were purchased from PerkinElmer (Waltham, MA) and Thermo Fisher Scientific (Waltham, MA), respectively. Cell culture media and supplements were from Cellgro (Manassas, VA), Gibco BRL (Grand Island, NY), or Sigma Aldrich (St. Louis, MO). Unless otherwise noted, all other reagents were from Sigma Aldrich (St. Louis, MO).
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2

Cell Culture Reagents and Standards

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Dulbecco’s modified Eagle’s medium (DMEM), fetal calf serum (FCS), and other cell culture reagents were purchased from Invitrogen (Thermo Fischer Scientific, Erembodegem, Belgium). Na125I and Iodogen® pre-coated tubes were from PerkinElmer Life Sciences and Pierce, respectively (both distributed by Thermo Fisher Scientific). Chloroquine was obtained from Sigma-Aldrich (Bornem, Belgium). Kaleidoscope SDS-PAGE molecular weight standards were from Bio-Rad Laboratories (Nazareth Eke, Belgium) and Himark prestained high-molecular-weight protein standard from Invitrogen. Pronase®, a mixture of proteinases isolated from the extracellular fluid of Streptomyces griseus, was from Roche Applied Science (Sigma-Aldrich).
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3

Quantifying Leukocyte-Endothelial Interactions

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Monoclonal mouse anti‐human ICAM‐1 (clone R6.5) was from ATCC (Manassas, VA) and phycoerythrin‐labeled monoclonal mouse anti‐human ICAM‐1 (clone LB‐2) was from Santa Cruz Biotechnology (Dallas, TX). Alexa Fluor 350‐labeled goat anti‐mouse IgG was from Invitrogen (Carlsbad, CA). Nonspecific mouse IgG was from Jackson ImmunoResearch (West Grove, PA). Green Fluoresbrite® polystyrene particles (100 nm in diameter) were from Polysciences (Warrington, PA). Porous transwell inserts (1.0 µm‐pore size) were from Thermo Fisher Scientific (Waltham, MA). Human sICAM‐1 ELISA kits were from Invitrogen (Carlsbad, CA). 125Iodine (125I) and Iodogen pre‐coated tubes were from PerkinElmer (Waltham, MA) and Thermo Fisher Scientific (Waltham, MA), respectively. MMP‐9 Inhibitor I and MMP‐2 Inhibitor I were from EMD Millipore (Billerica, MA). Unless specified, all other reagents were from Sigma‐Aldrich (St. Louis, MO).
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4

Quantifying ICAM-1 Expression in Endothelial Cells

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Mouse monoclonal anti-human ICAM-1 (clone R6.5) and rat monoclonal anti-mouse ICAM-1 (clone YN1) were obtained from hybridomas from American Type Culture Collection (Manassas, VA). Non-specific mouse IgG was from Jackson ImmunoResearch (West Grove, PA) and monoclonal anti-VE-cadherin was from Thermo Fisher Scientific (Waltham, MA). Texas Red-labeled secondary antibodies, Texas Red-labeled dextran (10,000 MW; lysine fixable), and Alexa Fluor 350-labeled secondary antibodies were from Invitrogen (Carlsbad, CA). Recombinant human acid sphingomyelinase (ASM) was provided by Dr. Edward Schuchman (Department of Genetics and Genomics Sciences, Mount Sinai School of Medicine, New York, NY). Fluoresbrite™ 100 nm diameter polystyrene beads were from Polysciences (Warrington, PA). Cell culture reagents were from Gibco-BRL (Grand Island, NY) or Cellgro (Manassas, VA). Porous transwell inserts (1.0 μm-diameter pore) were from Thermo Fisher Scientific (Waltham, MA). 125I and Iodogen pre-coated tubes were from Perkin Elmer (Waltham, MA) and Thermo Fisher Scientific (Waltham, MA), respectively. MMP-9 and MMP-2 inhibitors were from EMD Millipore (Billerica, MA). Recombinant human MMP-9 (67 kDa) and MMP-2 (62 kDa) were from EMD Millipore (Billerica, MA) and Sigma-Aldrich (St. Louis, MO), respectively.
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5

ICAM-1 Immunolabeling Protocol

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Monoclonal mouse anti-human ICAM-1 (clone R6.5) was from ATCC (Manassas, VA) and phycoerythrin-labeled monoclonal mouse anti-human ICAM-1 (clone LB-2) was from Santa Cruz Biotechnology (Dallas, TX). Alexa Fluor 350-labeled goat anti-mouse IgG was from Invitrogen (Carlsbad, CA). Non-specific mouse IgG was from Jackson ImmunoResearch (West Grove, PA). Green Fluoresbrite® polystyrene particles (100 nm in diameter) were from Polysciences (Warrington, PA). Porous transwell inserts (1.0 µm-pore size) were from Thermo Fisher Scientific (Waltham, MA). Human sICAM-1 ELISA kits were from Invitrogen (Carlsbad, CA). 125Iodine (125I) and Iodogen pre-coated tubes were from PerkinElmer (Waltham, MA) and Thermo Fisher Scientific (Waltham, MA), respectively. MMP-9 Inhibitor I and MMP-2 Inhibitor I were from EMD Millipore (Billerica, MA). Unless specified, all other reagents were from Sigma-Aldrich (St. Louis, MO).
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6

Monoclonal Anti-ICAM-1 Binding Assay

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Monoclonal mouse anti-human ICAM-1 (anti-ICAM) was clone R6.5 (ATCC; Manassas, VA). Non-specific mouse IgG and secondary goat anti-mouse IgG were from Jackson Immunoresearch (West Grove, PA). Fluoresbrite® polystyrene latex particles (not functionalized) were from Polysciences (Warrington, PA). 125Iodine (125I) and Iodogen pre-coated tubes were purchased from PerkinElmer (Waltham, MA) and Thermo Fisher Scientific (Waltham, MA), respectively. Unless otherwise noted all other reagents were from Sigma Aldrich (St. Louis, MO).
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