Rice Magnaporthe grisea DNA fingerprint belt-type encoding system classifying and analyzing method
A technology of DNA fingerprinting and analysis method, which is applied in the research and analysis of the variability of rice pathogens and the field of research and analysis of genetic traits of rice pathogen variability. It can solve problems such as different calculation formulas and standard naming pedigrees of band patterns, so as to avoid repeated research. , easy to interpret, and easy to compare with each other
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Embodiment 1
[0028] The rice blast fungus DNA fingerprint spectrum band type coding program classification and analysis method of the present embodiment is carried out specifically for the rice blast fungus in the japonica rice planting areas in Jiangsu and northern China, and its detailed process is as follows:
[0029] 1. Sampling
[0030] The rep-PCR band type and pedigree research The test materials come from panicle blast samples, which are collected from rice at the panicle stage in the five major rice regions of Jiangsu Province. The samples were isolated from single spores and used for genomic DNA extraction. The sample strains were cultured, sporulated and dried at low temperature and stored on rice straw and filter paper discs. The total number of samples analyzed by rep-PCR band pattern was 296.
[0031] 2. Genomic DNA extraction of Magnaporthe grisea
[0032] 2.1 Extract mycelium
[0033] Use the CTAB / NaCl micro-method to prepare the genomic DNA of Magnaporthe grisea. The m...
Embodiment 2
[0060] The method for classification and analysis of the rice pathogen DNA fingerprint spectrum band type coding program of the present embodiment is carried out specifically for the rice blast fungus in the southern rice region of China, and its detailed process is as follows:
[0061] 1. Sampling—collect 105 test strains from Zhejiang and North China, and isolate and cultivate the strains.
[0062] 1.1 Single spore isolation: Select 2-3 branches of panicle necks with typical symptoms from the standard sample collected, rinse the surface with clean water, soak in a small test tube for 6-8 hours until the standard sample is completely wet, and keep it moist for 24 hours at 26°C. About 1 hour (generally based on the sporulation of lesion spot), put the standard sample on the glass slide of the modified microscope, observe the sporulation situation under the microscope, pick out single spores with a needle fixed on the stage, and place them on the PDA. culture medium (potato, su...
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