Detect and quantify BK virus in blood or urine.
Quantitative Real-Time Polymerase Chain Reaction
New York DOH Approval Status
Lavender (EDTA), pink (K2EDTA) or serum separator tube OR urine.
Transport 1 mL whole blood, serum, plasma or urine in a sterile container. (Min: 0.5 mL).
Specimen source required.
Ambient: 24 hours; Refrigerated: 72 hours; Frozen: 1 month
The quantitative range of this assay is 2.6-8.6 log copies/mL (390-390,000,000 copies/mL).
A negative result (less than 2.6 log copies/mL or less than 390 copies/mL) does not rule out the presence of PCR inhibitors in the patient specimen or BK virus DNA concentrations below the level of detection of the assay. Inhibition may also lead to underestimation of viral quantitation.
Caution should be taken when interpreting results generated by different assay methodologies.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Analyte Specific Reagent (ASR)
The limit of quantification for this DNA assay is 2.6 log copies/mL (390 copies/mL). If the assay DID NOT DETECT the virus, the test result will be reported as "< 2.6 log copies/mL (< 390 copies/mL)." If the assay DETECTED the presence of the virus but was not able to accurately quantify the number of copies, the test result will be reported as "Not Quantified."
|Component Test Code*||Component Chart Name||LOINC|
|0090059||BK Virus Quant by PCR (log copy/mL)||43201-3|
|0093241||BK Virus Quant by PCR, Interp||47251-4|
|0096366||BK Virus Quant by PCR, Source||31208-2|
|2002302||BK Virus Quant by PCR (copy/mL)||48309-9|
- BK (Polyoma) Virus
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- BKV DNA
- Viral load monitoring