Total DNA extraction method for Eremochloa ophiuroides (Munro.) Hack.
An extraction method, the technology of the pseudo-threshold grass, which is applied in the field of molecular biology and can solve the problems of not being able to be applied well
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Embodiment 1
[0037] Select 2 parts of the current year's leaves (in mid-June) and 2 samples stored at -70°C for one month, a total of 4 genotypes, and use the method of the present invention to perform the following extractions:
[0038] A method for extracting the total DNA of Pseudomonas chinensis, characterized in that: the specific steps are as follows:
[0039] (1) Weigh 0.2g of Herba Cauliflower, grind it in a liquid nitrogen grinder, and transfer the finely ground Herba Cauliflower to a 2mL centrifuge tube;
[0040] (2) Add 0.7mL of CTAB extraction buffer and 14μL of β-mercaptoethanol to a 2ml centrifuge tube, cover the centrifuge tube, mix well, warm bath in 65°C water for 30min, during which time mix well by inversion 5-6 times; among them, The composition of CTAB extraction buffer is: 2%CTAB, 10mM Tris-HCl, 8mM EDTA, 1.4M NaCl, 5%PVP, pH 8.0;
[0041] (3) Take out the sample after the warm bath, cool it to room temperature, add 0.7mL of a mixture containing chloroform and isoamy...
Embodiment 2
[0056] Select 2 parts of the current year's leaves (in mid-June) and 2 samples stored at -70°C for one month, a total of 4 genotypes, and use the method of the present invention to perform the following extractions:
[0057] A method for extracting the total DNA of Pseudomonas chinensis, characterized in that: the specific steps are as follows:
[0058] (1) Weigh 0.2g of Herba Cauliflower, grind it in a liquid nitrogen grinder, and transfer the finely ground Herba Cauliflower to a 2mL centrifuge tube;
[0059] (2) Add 0.7mL of CTAB extraction buffer and 14μL of β-mercaptoethanol to a 2ml centrifuge tube, cover the centrifuge tube, mix well, warm bath in 65°C water for 30min, during which time mix well by inversion 5-6 times; among them, The composition of CTAB extraction buffer is: 2%CTAB, 10mM Tris-HCl, 8mM EDTA, 1.4M NaCl, 5%PVP, pH 8.0;
[0060] (3) Take out the sample after the warm bath, cool it to room temperature, add 0.7mL of a mixture containing chloroform and isoamy...
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