Cobas taqman manual

The COBAS AmpliPrep/COBAS TaqMan HCV Test is a nucleic acid amplification test for the quantitation of HCV RNA in human serum or plasma. Specimen preparation is automated using the COBAS AmpliPrep Instrument with amplification and detection automated using the COBAS TaqMan Analyzer or the COBAS TaqMan 48 Analyzer. On , the FDA approved the COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 Test. From the FDA website: “The COBAS AmpliPrep/COBAS TaqMan HIV-1 is an in vitro nucleic acid amplification test for the quantitation of Human Immunodeficiency Virus (HIV-1) nucleic acid in human plasma. The COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 Test, version (v) is an in vitro nucleic acid amplification test for the quantitation of Human Immunodeficiency Virus Type 1 (HIV-1) RNA in human EDTA plasma or from a cobas® Plasma Separation Card (PSC) dried.

Running the COBAS Ampliprep/COBAS TaqMan HIV-1 Qualitative Test 1. Go to Tasks – Assays on the menu bar or click the Assays () button on the LDMS toolbar. 2. Click the plus sign (+) next to the DNA PCR category. 3. Click COBAS TaqMan HIV-1 Qual.. (See Figure 1.). Figure 1: Assays. 4. Click Select Assay. (See Figure 2.) Figure 2: Assay. The COBAS® TaqMan® 48 Analyzer calculates the HCV RNA titer in the test samples by comparing the HCV signal to the HCV Quantitation Standard signal for each sample and control. COBAS® TaqMan® HBV Test For Use With The High Pure System FOR IN VITRO DIAGNOSTIC USE. COBAS' TaqMatCOBAS' TaqMatn" [HV Test Fier Use With Thie High Pite Syste, is atr 1t'renu¢/eicacid.

Since , studies on the diagnostic accuracy of COBAS TaqMan MTB (CTM) Higgins, J. P. Green, S. Cochrane handbook for systematic. The COBAS® TaqMan® MTB Test is based on two major processes: (1) manual specimen preparation to obtain MTB DNA; (2) simultaneous PCR amplification of target. 6 COBAS TaqMan Analyzers Common Features and Benefits Kinetic PCR Integrated Quantification Standard requires no external standard curves Closed Tube Format.