PCR detection method for quickly detecting large coptotermes formosunus
A detection method and rapid technology, applied in the field of PCR detection, can solve the problems of low reliability, low probability of winged adults, and poor accuracy, and achieve the effects of ensuring public health safety, maintaining ecological balance, and protecting production safety.
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Embodiment 1
[0040] This embodiment designs the specific primers of our termites. In the experiment, we use 6 kinds of termites to carry out PCR specificity to our termites, Coptotermes formosanus, Coptotermes saipang, Coptotermes indo-Burmese, Coptotermes termites and Coptotermes japonica. For testing, the sample numbers and sources are shown in the table below:
[0041]
[0042]
[0043] Such as figure 2 As shown, the designation of the routine PCR upstream primer number is CC-F5, located at the 407bp-427bp position of our termite ITS1, see sequence number NO.1; the downstream primer number is CC-R5, located at the 641bp-661bp position of our termite ITS2 For the position, see SEQ ID NO: 2, the size of the amplified fragment is 254bp.
[0044] The specific detection steps are:
[0045] For the preparation of DNA templates, a termite was taken, rinsed in double distilled water, blotted dry with absorbent paper, and its body surface attachments and abdominal contents were removed ...
Embodiment 2
[0050] This embodiment adopts real-time fluorescent PCR detection, (such as figure 2 Shown) fluorescent primers and probes are designed to be located at ITS2, the upstream and downstream primers and probes are numbered CC-F6, CC-R8 and CC-TZ-6 respectively, and the sequence numbers in the sequence list are NO.3 and NO. 4 and NO.5, the size of the predicted amplified fragment is 155bp, the upstream primer CC-F6 sequence is 5'-AGGCCGCGGGCCCGAAGATGG-3', the downstream primer CC-R8 sequence is 5'-CCGAGATCTCTCTCGTATTTTC-3', the primer probe CC- The sequence of TZ-6 is 5'-FAM-ACGACAGCACTGTCTTAATCTTCG-TAMRA-3'.
[0051] The basic detection steps are the same as in Example 1, the difference lies in the establishment of the PCR reaction system: the total volume is 20 μl, and the components are as follows: 2 μl of 10×PCR buffer, 2 μl of MgCl 2 (25mmol / mL), 1.6μl dNTP mixture (10mmol / mL each), 0.5μl each of upstream and downstream primers (CC-F6, CC-R8, 10μmol / mL), CC-TZ-6 probe (10μmo...
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