Rusty Palm Weevil Specific Primers and Rapid Molecular Detection Method
A specific, palm-based technology, applied in the field of PCR identification, which can solve the problems of laborious and time-consuming, achieve high sensitivity, accurate results, and avoid time-consuming effects
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Embodiment 1
[0033] The design of embodiment 1 primer
[0034] 1. The total DNA of 9 species of weevils was extracted using EZgene from BIOMIGA Company TM Insect gDNA Kit (GD2413-02) kit.
[0035] The 9 species of weevils are: 1-Rusty Palm Weevil Rhynchophorus.ferrugineus, 2-Cryptorrhynchus lapathi, 3-Ditch Orbital Elephant Eucryptorrhynchus.chinensis, 4-Ailanthus Eucryptorrhynchus brandti, 5-Mango Fruit Stone Weevil Odoiporus .longicollis, 6-banana corm weevil Cryptorrhynchus.lapathi, 7-mazon pine horn shin like Shirahoshizo patruelis, 8-corn like Sitophilus zeamais, 9-pine knot like Hyposipalus gigas.
[0036] 2. Amplification of weevil COI gene sequence
[0037] According to literature reports, synthetic weevil insect COI gene sequence amplification universal primers:
[0038] C1-J-2183:5'-CAA CAT TTATTT TGATTT TTT GG-3', (SEQ ID NO.5)
[0039] TL-2-N-3014: 5'-TCC ATT GCA CTA TAC TGC CAT ATT A-3' (SEQ ID NO.6)
[0040] PCR amplification reaction using GreenMaster Mix Kit (Promega...
Embodiment 2
[0056] The establishment of the PCR amplification method of embodiment 2 rapid detection rust color palm weevil
[0057] 1. PCR reaction system
[0058] The total DNA of the rust-colored palm weevil was used as a template for PCR reaction. The 25 μL reaction system is shown in Table 1.
[0059] 2. PCR reaction conditions
[0060] The following conditions were set for the reaction: pre-denaturation at 94°C for 2 min; denaturation at 94°C for 30 s, annealing at 53°C for 45 s, extension at 72°C for 2 min, 30 cycles; final extension at 72°C for 10 min.
[0061] 3. After the reaction, the digested product is judged by agarose gel electrophoresis. When PCR amplification is performed with the primers shown in SEQ ID NO.1-2, if the amplified product is 458bp, the insect sample to be tested is positive. Rusty palm weevil;
[0062] When performing PCR amplification with the primers shown in SEQ ID NO.3-4, if the amplified product is 454bp, the insect sample to be tested is positive, ...
Embodiment 3
[0063] The specificity and the sensitivity of embodiment 3 rust color palm weevil PCR method of the present invention
[0064] With the DNA of 9 kinds of weevil class insects commonly seen in China (see embodiment 1) as template, with the rusty color palm weevil DNA as positive control, the rusty color palm weevil SS-COI primer RFSSF1 / Species specificity of RFSSR1 and RFSSF2 / RFSSR2. Amplify with different concentrations of rust-colored palm weevil DNA standard as a template to test the sensitivity of the primers.
[0065] 1. Preparation of standard products
[0066] After the concentration and purity of the DNA of 9 kinds of weevils were determined, they were prepared into a mother solution with a concentration of 10 ng / μl. And the DNA samples of rust-colored palm weevil were diluted into 10ng / μl, 1ng / μl, 100pg / μl, 10pg / μl, 1pg / μl, 100fg / μl standard solution in sequence according to the ratio (1:10). All standard solutions were stored at 4°C for future use.
[0067] 2. Am...
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