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BK Virus DNA


                   Quantitative, Real-Time PCR, Plasma 11274 CPT Code(s): 87799 Preferred

                   Specimen(s) 0.7 mL plasma collected in an EDTA (lavender-top) tube or ACD
                   (yellow-top) tube or 0.7 mL serum collected in a Serum Separator Tube (SST®)

                   or 0.7 mL whole blood collected in an EDTA (lavender-top) tube or ACD

                   (yellow-top) tube Minimum Volume 0.3 mL Instructions For CSF order test
                   code 18901-BK Virus DNA, Quantitative Real-Time PCR, CSF and for urine

                   order test code 16581-BK Virus DNA, Quantitative Real-Time PCR, Urine.
                   Plasma: Collect blood in sterile tubes containing EDTA as an anticoagulant, or

                   in plasma preparation tube (PPT). Collect whole blood at room temperature

                   and separate plasma from cells within 2 hours of collection. Transfer plasma to
                   sterile, transport aliquot tubes. Freeze and ship frozen. Serum: Collect blood in

                   sterile tubes with no anticoagulants; Serum Separator Tubes (SST®) are
                   recommended. Allow blood to clot at room temperature and separate serum

                   within 1 hour of collection. Transfer serum to sterile, transport aliquot tubes.
                   Freeze and ship frozen. Whole Blood: Collect using standard procedures.

                   Store samples refrigerated following collection. Do not freeze whole blood.

                   Transport Container Tranport tube Transport Temperature Plasma or serum:
                   Frozen Whole blood: Refrigerated (cold packs) Specimen Stability Plasma and

                   serum Room temperature: 48 hours Refrigerated: 7 days Frozen: 30 days
                   Whole blood Room temperature: 48 hours Refrigerated: 8 days Frozen:

                   Unacceptable Reject Criteria Frozen whole blood • Samples collected in

                   heparin • Unspun PPT tube • Serum collected in a no additive (red-top) tube
                   Methodology Real-Time Polymerase Chain Reaction (RT-PCR) This test was

                   developed and its analytical performance characteristics have been
                   determined by Quest Diagnostics. It has not been cleared or approved by the

                   U.S. Food and Drug Administration. This assay has been validated pursuant to

                   the CLIA regulations and is used for clinical purposes. Performing Laboratory
                   Quest Diagnostics Infectious Disease, Inc. 33608 Ortega Highway, Bldg

                   B-West Wing San Juan Capistrano, CA 92675-2042 Setup Schedule Set up:
                   Daily; Report available: 1 day Reference Range(s)







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