cobas® ️TV/MG

Protocol tips

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• cobas® TV/MG for use on the cobas® 6800/8800 Systems is an automated, qualitative in vitro diagnostic test, that utilizes real-time polymerase chain reaction (PCR), for the direct detection of Trichomonas vaginalis (TV) and/or Mycoplasma genitalium (MG) DNA

Upstream tips
• cobas® TV/MG for use on the cobas® 6800/8800 Systems is an automated, qualitative in vitro diagnostic test, that utilizes real-time polymerase chain reaction (PCR), for the direct detection of Trichomonas vaginalis (TV) and/or Mycoplasma genitalium (MG) DNA

Publication protocol

The cobas TV/MG assay (Roche Diagnostics, Rotkreuz, Switzerland) performed on the cobas 6800 System (Roche Diagnostics) was used for detection of MG. The cobas TV/MG assay is a CE-marked, Food and Drug Administration–cleared, commercial qualitative nucleic acid test that utilises the real-time polymerase chain reaction for dual detection of Trichomonas vaginalis (TV) and MG. Its reported overall sensitivity and specificity rates were 83.1% and 98.4%, respectively, for MG detection in endocervical swabs from female patients.10 Tests were performed in accordance with the manufacturer’s instructions.

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Manufacturer protocol

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