Harmonia axyridis specific COI primer of harmonia axyridis, kit containing primer and detection method for harmonia axyridis
The technology of a heterochromia and detection method, applied in the field of molecular biology, can solve the problems that the specific detection method of heterochromia has not been established, and cannot accurately evaluate the predation effect of ladybugs in the ladybug group, and achieve high practical value , high accuracy and simple operation
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Embodiment 1
[0023] Example 1 The amplification effect of primer HaF3 / HaR3 on the heterochromia
[0024] 1. Preparation of Heterochromia genome
[0025] Put a single Heterochromia in a 1.5mL centrifuge tube and grind it, and use TIANamp Genomic DNA Kit blood / cell / tissue genomic DNA extraction kit (spin column type) (Tiangen Biological Co., Ltd., Beijing) to extract single The head ladybug genome. The DNA solution was stored at -20°C for later use, and 1 μL of the solution was taken as a DNA template during PCR amplification.
[0026] 2. Synthesis of specific COI primers for the detection of Heterochromia
[0027] The specific COI primer sequences are as follows:
[0028] HaF3: 5'-AATTGTTACAGCTCATGCT-3' (SEQ ID No. 1)
[0029] HaR3: 5'-CCCCTATTTCTACGATTG-3' (SEQ ID No. 2)
[0030] 3. PCR amplification
[0031] The reaction system is 20 μL, including: 10×EasyTaq buffer 2.0 μL, dNTP (2.5 mM) 0.4 μL, EasyTaq DNA polymerase (5U / μL) 0.2 μL, forward and reverse primers (10 μM) each 0.4 μL, ...
Embodiment 2
[0040] Example 2 Primer HaF3 / HaR3 Determination of the Minimum Detection Amount of Heterochromia
[0041] 1. Preparation of Heterochromia template DNA
[0042] According to Example 1, the single Heterochromia genomic DNA was extracted, and then the original template solution (the concentration of the DNA solution was 3ng / μL) was diluted by 2 times until no bands were detected, and 1 μL was used as the template for PCR amplification. Add directly to the PCR reaction system, and the reaction system is the same as that described in Example 1.
[0043] Using the primers HaF3 / HaR3 to determine the minimum detection amount, PCR amplification was carried out with different dilutions of the heterochromia genome DNA as a template, and the detection limit of the DNA concentration was 0.01171875ng / μL ( figure 2 ).
[0044] 2. Preparation of Heterochromia plasmid
[0045] According to the implementation example 1, the genomic DNA of the ladybug heterochromia was amplified, and after t...
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