Fluorescent quantitative PCR (polymerase chain reaction) kit for quickly detecting gonococcus
A fluorescent quantitative, gonococcal technology, applied in the rapid detection of gonococcus fluorescent quantitative PCR detection method and its kit, the field of qualitative and quantitative detection of gonococcus, can solve the problems of poor specificity, time-consuming and laborious, and inability to accurately quantify
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Embodiment 1
[0040] Embodiment 1: kit composition and preparation
[0041] a. DNA extraction reagent
[0042] DNA lysate composition:
[0043] Lysis solution I: prepare 0.01M PBS (28.94g Na 2 HPO 4 12H 2 O, 2.6 g KH 2 PO 4 2H 2 O add 1000ml ultra-clean water and mix well, adjust the pH to 7.4).
[0044]Lysis Solution II: In pH7.4 Tris-EDTA buffer (pH7.610mM Tris.HCL, pH8.01mMEDTA), add NP-40 according to the ratio of 1:100 and mix well to complete the preparation. Divide the extract II into 5ml cryopreservation tubes (transparent tubes with lids). The filling volume is 5ml / tube.
[0045] b. Composition of fluorescent PCR 10×Buffer:
[0046] 500mM KCl, 100mM Tris-HCl (PH9.025°C), 1.0% Triton X-100;
[0047] c. Fluorescent quantitative PCR reaction solution: PCR 10×buffer 5.0 μl, 10 μmol / L forward primer and reverse primer 1.5 μl each, 5 μmol / L fluorescent probe 1.5 μl, 25 mmol / L MgCl 2 12.5μl, 10mmol / L dNTPs 1.0μl, 2.5U / μl Taq DNA polymerase 1.0μl, sterile double distilled water...
Embodiment 2
[0050] Example 2: Rapid detection of Neisseria gonorrhoeae using a kit
[0051] a. DNA extraction process:
[0052] ① Transfer 500μl of the liquid in the centrifuge tube to a 1.5ml centrifuge tube, and centrifuge at 12000rpm for 5min;
[0053] ②Discard the supernatant, add 500μl extract solution I, and centrifuge at 12000rpm for 5min;
[0054] ③Discard the supernatant, add 200μl extract solution I, and centrifuge at 12000rpm for 5min;
[0055] ④ Discard the supernatant and add 50 μl of extraction solution II;
[0056] ⑤ Oscillating and mixing, 100 ℃ constant temperature treatment for 10 minutes;
[0057] ⑥ Centrifuge at 12,000 rpm for 5 minutes, and take 5 μl of the supernatant for PCR amplification.
[0058] b. Serially dilute the positive standard template (reagent d) to 10 8 copies / ml, 10 7 copies / ml, 10 6 copies / ml, 10 5 copies / ml, 10 4 copies / ml, 10 3 copy / ml.
[0059] c. Take 45 μl each of the fluorescent quantitative PCR reaction solution (reagent c), 5 μl ea...
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