Product DetailsRecommended AssayReferencesDescriptionBD TruCOUNT™ Control beads are designed for use with in vitro diagnostic products such as BD TriTEST™ reagents and a suitably equipped flow cytometer for use as a control for certain elements of the absolute counting process. Specifically, a control bead value that is outside the expected range could indicate an error in pipetting or a problem with the value from the Absolute Count Beads. TruCOUNT Control beads are not intended as a substitute for a cellular control. TruCOUNT Controls can be used with the FACS Loader.Resources & ToolsSpectrumViewerDownload MSDSPreparation and StorageTruCOUNT Control beads are sensitive to compensation, specifically in FL2–%FL1. If lyse/no-wash procedures are not employed, care must be taken to ensure FL2 brightness is adequate. Store at 2° to 8°C. Do not use after expiration date on vial.Clinical Applications of Flow Cytometry: Quality Assurance and Immunophenotyping of Peripheral Blood Lymphocytes. Villanova, PA: National Committee for Clinical Laboratory Standards; 1992. NCCLS document H42-T.Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture. Villanova, PA: National Committee for Clinical Laboratory Standards; 1991.Protection of Laboratory Workers from Infectious Disease Transmitted by Blood, Body Fluids, and Tissue: Tentative Guideline. Villanova, PA: National Committee for Clinical Laboratory Standards; 1991. NCCLS document M29-T2.Centers for Disease Control. Update: universal precautions for prevention of transmission of human immunodeficiency virus, hepatitis B virus, and other bloodborne pathogens in healthcare settings. MMWR. 1988;37:377-388.Jackson A, Warner N. Preparation, staining, and analysis by flow cytometry of peripheral blood leukocytes. In: Rose N, Friedman H, Fahey J, ed. Manual of Clinical Laboratory Immunology. 1986:226-235.Nicholson JK, Browning SW, Orloff SL, McDougal JS. Inactivation of HIV-infected H9 cells in whole blood preparations by lysing/fixing reagents used in flow cytometry. J Immunol Methods. 1993;160:215-218.
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