User Guide for hygiena models including: MON810, MON810 GMO Maize Detection Kit, GMO Maize Detection Kit, Maize Detection Kit, Detection Kit, Kit
Identificación de OMG | Hygiena
Dec 15, 2023 — Verify results of positive (Control Template) and negative (H2O) controls, before interpreting the sample results. Always compare samples to positive and ...
GMO MON810 Maize Detection Kit | Hygiena
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DocumentDocumentfoodproof® SL GMO MON810 Maize Detection Kit Ready Reference Guide Product No. KIT230205 Revision A, December 2023 PCR kit for the qualitative detection of MON810 DNA using real-time PCR instruments. Before starting, it is strongly recommended to read the entire product manual available on our website. PROGRAM SETUP Program your real-time PCR instrument before setting up the PCR reactions. Select the following channels: u FAM (MON810) and VIC/HEX (Internal Control). 95 °C 60 °C 50 °C 2 min | 10 min 1 cycle 15 sec | 60 sec* 45 cycles Pre-incubation: 1 cycle Step 1: 50 °C for 2 min Step 2: 95 °C for 10 min Amplification: 45 cycles Step 1 : 95 °C for 15 sec Step 2*: 60 °C for 60 sec * Fluorescence detection DATA INTERPRETATION Verify results of positive (Control Template) and negative (H2O) controls, before interpreting the sample results. Always compare samples to positive and negative controls. Review data from each channel and interpret results as described in the table. FAM + - VIC/HEX + or + - Result Interpretation Positive for MON810 Negative for MON810 Invalid RR-KIT230205-RevA foodproof® is a registered trademark of Hygiena. The above mentioned real-time PCR instruments are registered trademarks of their respective holders. PREPARATION OF THE PCR MIX Take appropriate precautions to prevent contamination, e.g., by using filter tips and wearing gloves. Thaw reagents, mix (do not vortex!) and briefly spin vials before opening. +12.5 µL + 4 µL + 3.5 µL 1. PREPARE PCR MIX Add 12.5 µL Master Mix (2XM), 4.0 µL Primer/Probe Mix (P) and 3.5 µL PCR-grade H2O (not included) for each reaction to a suitable tube. (n samples + 2 controls + at least one additional reaction to cover pipetting loss). Mix carefully but thoroughly by pipetting up and down. +20 µL 2. ADD PCR MIX Pipette 20 µL of prepared PCR mix into each strip or plate well. +5 µL 3. ADD SAMPLES AND CONTROLS Pipette 5 µL of samples, negative control (PCR-grade H2O) or Control Template (C) into respective wells. 4. SEAL Carefully seal strips/plate. 5. CENTRIFUGE Briefly spin strips/plate in a suitable centrifuge. 6. START REAL-TIME PCR RUN Cycle samples as described above. foodproof® SL GMO MON810 Maize Detection Kit KIT230205 For food testing purposes Kit for 50 reactions FOR IN VITRO USE ONLY Store kit at -15 to -25 °C Hygiena® | Camarillo, CA 93012 USA | diagnostics.support@hygiena.com | www.hygiena.com