A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
BK Virus DNA, Quantitative Real-Time PCR, Plasma
MessageEffective 06/08/2024: Test is being replaced by BKVG / LAB17071 Plasma, BK Virus DNA, Quantitative RT PCR performed at Inova Laboratories.
Test Code
Alias/See Also
Epic: LAB1374
CPT Codes
<p>87799</p>
Preferred Specimen
Submit only 1 of the following specimens:
Specimen Type: Whole Blood
Collection Container/Type
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD A or B)
Specimen Volume: 0.7 mL
Collection Instructions:
- Collect using standard procedures. Store samples refrigerated following collection. Do not freeze whole blood.
Specimen Type: Plasma EDTA
Collection Container/Type: Lavender top (EDTA)
Submission Container/Tube: Plastic vial
Specimen Volume: 0.7 mL
Collection Instructions:
- 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, plastic, screw-cap aliquot tubes. Freeze and ship frozen.
Specimen Type: Serum
Collection Container/Type: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.7 m:
Collection Instructions:
- Collect blood in sterile tubes with no anticoagulants; Serum Separator Tubes (SST ®s) are recommended. Allow blood to clot at room temperature and separate serum within 1 hour of collection. Transfer serum to sterile, plastic, screw-cap aliquot tubes. Freeze and ship frozen.
Minimum Volume
0.3 mL
Instructions
Transport Temperature
Specimen Stability
Whole Blood
Room temperature: 48 hours
Refrigerated: 8 days
Frozen: Unacceptable
Plasma or Serum
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Samples collected in heparin • Unspun PPT tube • Frozen whole blood • 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.
Setup Schedule
Report Available
1 day
Reference Range
BK Virus DNA, QN PCR | Not Detected (IU/mL) |
BK Virus DNA, QN PCR | Not Detected (Log IU/mL) |
Clinical Significance
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153
Last Updated: June 3, 2024