A method for identification of leaf defoliation and non-defoliation strains of Verticillium dahliae in cotton
A technology of cotton verticillium dahliae and its identification method, which is applied in the field of identification of verticillium dahliae, can solve the problems of low accuracy, low detection efficiency, and long detection cycle, etc., so as to improve the detection rate, save consumables, and high identification efficiency Effect
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Embodiment 1
[0033] Embodiment one: the method for identifying the defoliation type and non-defoliation type strains of Verticillium dahliae of cotton
[0034] The present invention provides a method for identifying the defoliation type and non-defoliation type strains of Verticillium dahliae of cotton, the identification method needs to use one specific primer to carry out one PCR reaction, specifically comprising the following steps:
[0035] (1) Extract the genomic DNA of the sample to be tested;
[0036] (2) Utilize specific primers to carry out PCR reaction;
[0037] The PCR reaction system is as follows:
[0038] 2×Tap PCR Green Mix 12.5ul, Template DNA 1.0μL, primer (10uM) 1μL, ddH2O 10.5μL, total 25μL;
[0039] The PCR reaction procedure is as follows:
[0040] Pre-denaturation at 94°C for 4 minutes, enter cycle, denaturation at 94°C for 30 s, annealing at 55°C for 45 s, extension at 72°C for 1 min, 30 cycles, extension at 72°C for 10 min;
[0041] (3) The PCR reaction product ...
Embodiment 2
[0044] Embodiment two: the present invention is verified to the effect of known bacterial strain
[0045] Utilize known bacterial strain to carry out effect verification to the identification method provided by the present invention:
[0046] (1) Prepare sample strains: 4 well-known deciduous strains and 4 non-deciduous strains;
[0047] (2) extract the genomic DNA of the sample to be tested;
[0048] (3) Utilize specific primers to carry out PCR reaction;
[0049] The PCR reaction system is as follows:
[0050] 2×Tap PCR Green Mix 12.5ul, Template DNA 1.0μL, Primer (10uM) 1μL, ddH 2 O 10.5 μL, 25 μL in total;
[0051] The PCR reaction procedure is as follows:
[0052] Pre-denaturation at 94°C for 4 minutes, enter cycle, denaturation at 94°C for 30 s, annealing at 55°C for 45 s, extension at 72°C for 1 min, 30 cycles, extension at 72°C for 10 min;
[0053] (4) The PCR product is detected by 1% agarose gel electrophoresis, and it can stably amplify 5 obvious bands for dec...
Embodiment 3
[0055] Embodiment three: the comparative experiment of the present invention and existing identification method
[0056]1. Prepare 7 well-known and recognized deciduous strains and 2 non-deciduous strains, respectively use the identification method provided by the present invention and the existing molecular detection using deciduous specific primers D1 / D2 and non-deciduous specific primers ND1 / ND2 The method was identified, and the results can be found in the appendix figure 2 .
[0057] attached by figure 2 It can be known that Figure A utilizes the identification method provided by the present invention to detect 7 deciduous bacterial strains and 2 non-deciduous bacterial strains at one time, and the detection rate is 100%; Figure B deciduous specific primer D1 / D2 detects 7 deciduous bacterial strains. There are 2 deciduous bacterial strains, and the non-deciduous specific primers ND1 / ND2 in Figure C detected 2 non-deciduous bacterial strains, and the detection rate was...
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