Primer and probe for real-time fluorescence PCR (polymerase chain reaction) detection of goose down component
A real-time fluorescence and probe technology, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., can solve the problems of high subjectivity, high requirements for inspectors, and easy misjudgment, and achieve Easy operation, high sensitivity and strong specificity
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[0036] 1. Take samples from unused parts of down jackets or other down products, and take a total of about 1g of samples. Cut the sample into pieces with scissors, disperse and mix them with an analytical grinder, then cut them into pieces with scissors as much as possible to less than 2mm, and mix them with an analytical grinder again.
[0037] 2. Weigh about 5 mg of sample from the mixed sample, put it into a 2mL centrifuge tube, extract 2 tubes in parallel for each sample, add 180 μL of buffer GL (Buffer GL), 20 μL of proteinase K (Proteinase K) and 10 μL of ribonuclease A (RNase A, 10 mg / mL), warmed in a 56°C water bath until the tissue was completely lysed for 3 hours. If the remaining fibrous tissue cannot be completely lysed, centrifuge at 12,000 rpm for 2 minutes after lysing to remove impurities before performing subsequent operations. Add 200 μL of Buffer GB (Buffer GB) and 200 μL of 100% ethanol to the lysate, and mix well by pipetting. During the warm bath, the s...
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