Method for analyzing corn borer population genetic diversity by ISSR system
A genetic diversity and corn borer technology, applied in the field of molecular biology, can solve the problem of less research on the genetic diversity of corn borer populations, and achieve the effects of high polymorphism, stable PCR amplification reaction, and clear amplification fragments
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specific Embodiment approach 1
[0040] Specific embodiment one: a kind of ISSR molecular marker primer that is used for the genetic diversity analysis of corn borer population of the present embodiment, described primer sequence comprises:
[0041] Primer 807: its nucleotide sequence is shown in the sequence table Seq ID No: 1;
[0042] Primer 810: its nucleotide sequence is shown in the sequence table Seq ID No: 2;
[0043] Primer 818: its nucleotide sequence is shown in the sequence table Seq ID No: 3;
[0044] Primer 825: its nucleotide sequence is shown in the sequence table Seq ID No: 4;
[0045] Primer 826: its nucleotide sequence is shown in the sequence table Seq ID No: 5;
[0046] Primer 835: its nucleotide sequence is shown in the sequence table Seq ID No: 6;
[0047] Primer 836: its nucleotide sequence is shown in the sequence table Seq ID No: 7;
[0048]Primer 847: its nucleotide sequence is shown in the sequence table Seq ID No: 8;
[0049] Primer 848: its nucleotide sequence is shown in th...
specific Embodiment approach 2
[0055] Embodiment 2: An ISSR-PCR reaction system for analyzing the genetic diversity of corn borer populations in this embodiment, each 25 μL reaction system contains 1 μL of template, 0.125 μL of Taq enzyme, 2.5 μL of Buffer, 2 μL of dNTP, and 1 μL of primer , ddH 2 O18.375 μL; Amplify the above reaction system according to the following procedure: pre-denaturation at 94°C for 5 minutes, denaturation at 94°C for 45 seconds, annealing at 40-61°C for 1.5 minutes, extension at 72°C for 1.5 minutes, a total of 40 cycles, and finally extension at 72°C for 10 minutes , stored at 4°C.
specific Embodiment approach 3
[0056] Embodiment 3: This embodiment is different from Embodiment 2 in that the primer is selected from any one of Seq ID Nos: 1-14 described in Embodiment 1.
[0057] Others are the same as in the second embodiment.
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