Metamycoplasma hominis, Molecular Detection, PCR, Plasma
Use
Rapid, sensitive, and specific identification of Metamycoplasma hominis from plasma. This test is not intended for medicolegal use.
Special Instructions
The specimen is not intended for medicolegal use. The high sensitivity of amplification by PCR requires the specimen to be processed in an environment in which contamination by M. hominis DNA is unlikely. NY State approval: Yes.
Limitations
A negative PCR does not rule out infection because false-negative results may occur due to PCR inhibition, sequence variability affecting primers and probes, or quantities below limit of detection. This test does not detect other species of Metamycoplasma or Ureaplasma.
New York Approved
Methodology
PCR-based (PCR)
Biomarkers
LOINC Codes
- 68546-1
- 68546-1
- 31208-2
Result Turnaround Time
3-4 days
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
1 mL
Minimum Volume
0.5 mL
Container
Lavender top (EDTA); acceptable: Royal blue top (EDTA), pink top (EDTA); submission: screw-capped, sterile container
Collection Instructions
Centrifuge and aliquot plasma into a sterile vial within 24 hours of collection.
Storage Instructions
Ship specimen refrigerated.
Causes for Rejection
All specimens will be evaluated for test suitability.
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 7 days |
| Frozen | 7 days |