A Rapid Identification Method of Lucilia sericata
A mercerized green fly, fast technology, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc., can solve the difficulty of classification and identification, and it is difficult for non-insect professionals to identify morphological species, long issues of time
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[0026] S1, 8 species of the residual limbs were collected by geldens and extracted DNA samples separately, and the resulting DNA sample was labeled as 1-8, respectively;
[0027] Among them, after cleaning in deionized water, the water absorbing paper was suiled and centrifugally, and the Takara mini Best kit was used to extract DNA, 4 ° C.
[0028] S2, design specific primers and treat samples for PCR amplification;
[0029] Among them, the specific primer sequence is:
[0030] 5'-cttgaccctgcaggaggag-3 ', as shown in SEQ ID NO.1;
[0031] 5'-agctaatatgcataatcatcccct-3 ', as shown in SEQ ID NO.2;
[0032] The PCR amplification system is: 2 × premix TAQ solution 5 ul, two primer sequence solutions 0.6 uul, the primer sequence is 10 umol / L, sample DNA template 1.3 ul, DDH 2 O Adhesive 10UL;
[0033] PCR amplification conditions were: 95 ° C pre-degeneration 1min; 94 ° C for 40 seconds, 68.3 ° C for 45 seconds, 72 ° C for 40 seconds, a total of 32 cycles; 72 ° C extends 8 min, and ...
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