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10) Prepare the appropriate number of strip tubes by transferring 10 µL of reconstituted
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assay to reaction tubes. Pipette 10 µL of extracted sample DNA into each sample
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strip tube and mix by pipetting up and down 2-3 times.
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5
11) Prepare the positive control tube by pipetting 10 µL of the Positive Control DNA
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into a strip tube containing 10 µL of reconstituted assay. Prepare the negative
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control by pipetting 10 µL of RNase-free water into a strip tube with 10 µL of
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reconstituted assay.
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12) Seal the strip tubes with the strip tube caps.
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13) Load sample tubes into the 72-well rotor and load into the Rotor-Gene-Q and
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initiate analysis immediately.
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(b)
Automated QIAsymphony
®
DNA Extraction Method
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1)
Ensure the “Waste” drawer is prepared properly, and perform an inventory scan of
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the “Waste” drawer, including the tip chute and liquid waste. Replace the tip
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disposal bag, if necessary.
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2)
Load an elution microtube rack (EMTR) into the “Eluate” drawer and perform an
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inventory scan of the “Eluate” drawer.
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3)
Load the QIAsymphony
mericon
Bacteria Kit and consumables into the “Reagents
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and Consumables” drawer. Select the “R+C” button in the touchscreen to open the
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screen that shows the consumables status (“Consumables/8-RodCovers/Tubes/
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Filter-Tips/Reagent Cartridges”). Select the “Scan Bottle” button to scan the bar
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code of the TopElute bottle with the handheld bar code scanner. Select the “OK”
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button.
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4)
Perform an inventory scan of the “Reagents and Consumables” drawer.
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5)
Transfer 500 µL of the enriched sample into a 2 mL screw cap tube. Place the
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samples into the appropriate tube carrier and load them into the “Sample” drawer.
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6)
Using the touch screen, enter the required information for each batch of samples to
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be processed.
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7)
Choose elution volumes according to Table B.
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OMAMAN-36 A : Collaborative Study Manuscript
For ERP Use Only
January 2017
AOAC Research Institute
Expert Review Panel Use Only