Method for rapid identification of aldrichina grahami
A technology of alblefly and giant tail, which is applied in the field of molecular biological identification, can solve the problems that non-insect professionals are difficult to identify the morphological species, the exact identification of necrophagous flies, the difficulty of classification and identification, etc., to achieve shortened Forensic identification period, overcoming the difficulty of morphological identification, and high sensitivity
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[0026] S1, 8 species of necrophagic flies were collected from the site and DNA samples were extracted respectively. The obtained DNA samples were samples to be identified and marked as 1-8 respectively;
[0027] Among them, the residual limbs of flies were washed with deionized water, blotted dry with absorbent paper, placed in a centrifuge tube, cut into pieces with ophthalmic scissors, and DNA samples of fly tissues were extracted by the conventional Chelex-100-proteinase K method, and stored at 4°C.
[0028] S2, designing specific primers and performing PCR amplification on the sample to be identified;
[0029] Wherein, the specific primer sequence is:
[0030] 5'-aatggggctggaacaggatg-3', as shown in SEQ ID NO.1;
[0031] 5'-aagctcgtgtgtctacgtct-3', as shown in SEQ ID NO.2;
[0032] The PCR amplification system is: 5ul of 2×Premix Taq solution, 0.4ul of each of the two primer sequence solutions, the concentrations of the primer sequence solutions are both 10umol / L, 1.2ul ...
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