A rapid dual PCR method for genotype identification of duck circovirus
A duck circovirus and genotype technology, applied in biochemical equipment and methods, recombinant DNA technology, and microbial determination/inspection, etc., can solve the problem of inability to distinguish between two genotypes of DuCV mixed infection and so on
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[0023] 1 Primer design
[0024] By comparing the published sequences of DuCV-1 and DuCV-2 on the reference GenBank, select the conserved regions of DuCV-1 and DuCV-2 to design a pair of general specific primers SEQ1 / SEQ2, 1 for DuCV respectively The type duck circovirus specific primer SEQ3 and the type 2 duck circovirus specific primer SEQ4 were used to amplify the two virus samples by conventional methods.
[0025] SEQ1: 5'-CGGGAAATGACGTAGTCGTCATG-3',
[0026] SEQ2: 5'-GG(A / C)(C / T)T(G / A)AACATGAGATGGGC-3',
[0027] SEQ3: 5'-GTTCACTCC(G / T)GTTGTGTTGTC(C / T)GG-3',
[0028] SEQ4: 5'-GATAATGCGAC(C / T)GGCGACG-3';
[0029] DuCV's universal primers SEQ1 / SEQ2 amplified fragment size is 1032bp, DuCV-1 specific primers SEQ2 / SEQ3 amplified fragment size is 446bp, DuCV-2 specific primers SEQ1 / SEQ4 amplified fragment size is 599bp. All primers were sterile ddH 2 O (Rnasefree) was prepared at a concentration of 25 pmol / μl for use.
[0030] 2DNA extraction
[0031] The total DNA of vari...
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