Reagent Kit for Detection and Identification of Ureaplasma urealyticum and Ureaplasma parvum by Polymerase Chain Reaction with Real-Time Detection, DIPLEX Uu+Up for In Vitro Diagnostics according to TU 21.20.23-515-17253567-2017

Reagent Kit for Detection and Identification of Ureaplasma urealyticum and Ureaplasma parvum by Polymerase Chain Reaction with Real-Time Detection, DIPLEX Uu+Up for In Vitro Diagnostics according to TU 21.20.23-515-17253567-2017

The reagent kit for detecting and identifying Ureaplasma urealyticum and Ureaplasma parvum using the polymerase chain reaction (PCR) method with real-time detection, DIPLEX Uu+Up, is intended for in vitro diagnostics.

Reagent Kit Options:

1. DIPLEX Uu+UP-РВ-120

• Reaction mixture RV, 960 µl - 1 vial
• Taq polymerase, 50 µl - 1 vial
• Diluent, 2 ml - 2 vials
• PCR Internal Positive Control (IPC), 200 µl - 1 vial

2. DIPLEX Uu+UP-OneStep-PB-60

• Amplification mixture PB-OS, 28 µl - 60 vials
• Diluent, 1 ml - 1 vial
• PCR Internal Positive Control (IPC), 100 µl - 1 vial

3. DIPLEX Uu+UP-OneStep-PB-96

• Amplification mixture PB-OS, 28 µl - 96 vials
• Diluent, 1 ml - 1 vial
• PCR Internal Positive Control (IPC), 100 µl - 1 vial

4. DIPLEX Uu+UP-TwoStep-PB-60

• Reaction mixture PB-TS, 21 µl - 60 vials
• Taq polymerase solution, 500 µl - 1 vial
• Diluent, 1 ml - 1 vial
• PCR Internal Positive Control (IPC), 100 µl - 1 vial

5. DIPLEX Uu+UP-TwoStep-PB-96

• Reaction mixture PB-TS, 21 µl - 96 vials
• Taq polymerase solution, 800 µl - 1 vial
• Diluent, 1 ml - 1 vial
• PCR Internal Positive Control (IPC), 100 µl - 1 vial

III. Usage Instructions

The kit includes brief instructions for the use of the reagents in performing the polymerase chain reaction.

IV. Information Leaflet

The information leaflet provides detailed information on the use and purpose of the PCR Internal Positive Control (IPC).

V. Product Passport

The documentation includes a product passport specifying the characteristics and technical data of the reagent kit.

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The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.