Primer and prober for detecting carrot component in foods and beverages
A carrot and probe technology, applied in the field of rapid detection of plant-derived components, can solve problems such as unidentification, discrepancies between product real attributes and labels, and reduction of raw material consumption
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Embodiment 1
[0033] Follow the procedure below for testing:
[0034] (1) Extraction of DNA from carrot noodle samples to be tested
[0035]A. Weigh 0.1g of carrot noodles, cut into pieces, and transfer to a 1.5mL centrifuge tube. Add 600 μL of preheated lysis buffer, mix gently, and keep warm in a water bath at 65°C for 10 minutes;
[0036] B. Add an equal volume of 600 μL of phenol / chloroform into the tube, mix well by inverting up and down, and extract for 2 minutes;
[0037] C. Centrifuge at 12000g for 5min, draw the supernatant into a new centrifuge tube, add the same volume of sedimentation solution as the supernatant, mix well, leave at room temperature for 10min, centrifuge at 12000g for 5min, remove the supernatant, and keep the precipitate;
[0038] D. Add 60 μL of RNase to the precipitate, place it at 37°C for 2 minutes, mix it well with a pipette tip, dissolve the precipitate at 37°C, add 300 μL of buffer solution after 5 minutes, and mix up and down 10 times;
[0039] E. Tak...
Embodiment 2
[0054] Follow the procedure below for testing:
[0055] (1) Extraction of the DNA of the tomato rice flour sample to be tested
[0056] A. Weigh 0.1g of tomato rice flour and transfer it to a 1.5mL centrifuge tube. Add 600 μL of preheated lysis buffer, mix gently, and keep warm in a water bath at 65°C for 10 minutes;
[0057] B. Add an equal volume of 600 μL of phenol / chloroform into the tube, mix well by inverting up and down, and extract for 2 minutes;
[0058] C. Centrifuge at 12000g for 5min, draw the supernatant into a new centrifuge tube, add the same volume of sedimentation solution as the supernatant, mix well, leave at room temperature for 10min, centrifuge at 12000g for 5min, remove the supernatant, and keep the precipitate;
[0059] D. Add 60 μL of RNase to the precipitate, place it at 37°C for 2 minutes, mix it well with a pipette tip, dissolve the precipitate at 37°C, add 300 μL of buffer solution after 5 minutes, and mix up and down 10 times;
[0060] E. Take ...
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