Roche Diagnostics Cobas™ Liat CT/NG/MG RT-PCR Assay Kit

Catalog No.	Quantity
21-200-310	20 tests per kit

Catalog No. 21-200-310 Supplier Roche Diagnostics Supplier No. 09449604190

Description

The Cobas™ liat CT/NG/MG test is an automated, qualitative in vitro nucleic acid diagnostic using real-time PCR for the detection of CT, NG, and MG in male urine and vaginal swabs.

The cobas™ liat CT/NG/MG nucleic acid test is an automated, qualitative in vitro nucleic acid diagnostic test that utilizes real- time polymerase chain reaction (PCR) for the direct detection of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), and Mycoplasma genitalium (MG) nucleic acid in male urine and vaginal swabs, all in cobas™ PCR Media (Roche Molecular Systems, Inc.). This test is intended as an aid in the diagnosis of urogenital infections in both symptomatic and asymptomatic patients.

Specifications

• Content And Storage: 20 tests per kit; store at 2° to 8 °C
• Clia Complexity: Waived
• Detectable Analytes: Chlamydia trachomatis, N. gonorrhoeae, Mycoplasma IgG
• Sensitivity: Chlamydia: male urine (97.3%); vaginal swab (98.2%). Gonorrhea: male urine (100.0%); vaginal swab (97.7%). Mycoplasma Genitalium: male urine (97.1%); vaginal swab (95.2%)
• Type: PCR test
• For Use With (Application): The cobas™ liat CT/NG/MG test is an automated, qualitative in vitro nucleic acid diagnostic using real-time PCR for the detection of CT, NG, and MG in male urine and vaginal swabs. For use with the cobas liat system.
• Includes: 20 tests per kit; pipettes
• Quantity: 20 tests per kit
• Specificity: Chlamydia: male urine (99.9%); vaginal swab (99.8%). Gonorrhea: male urine (99.9%); vaginal swab (99.8%). Mycoplasma Genitalium: male urine (99.2%); vaginal swab (97.8%)
• Analysis Time: 20 minutes
• Dimensions (L x W x H): 10.7 x 6.5 x 5.7 in.
• Weight (English): 2.4 lb.
• Form: Ready-to-Use (RTU)
• Operating Temperature Range: 2°C to 8°C