Method for extracting mitochondrial DNA of cotton
A technology for mitochondria and cotton, applied in the field of mitochondrial DNA extraction from cotton, can solve the problems of extremely complex influencing factors, influencing experiments, and high cost
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Embodiment 1
[0037] Embodiment 1, the extraction of cotton mitochondrial DNA
[0038] 1. Solution preparation
[0039] Buffer A was prepared as follows: Dilute 0.05 mol Tris-HCl, 1.2 mol NaCl, 2 mmol EDTA, 8 g polyvinylpyrrolidone (PVP), 4 mmol β-mercaptoethanol and 0.5 g bovine serum albumin (BSA) to 1 L with water , adjust the pH value to 8.0.
[0040] The preparation method of buffer B is as follows: 0.05mol Tris-HCl, 0.3mol sucrose, 0.03mol MgCl 2 and 3 g of polyvinylpyrrolidone (PVP) were adjusted to 1 liter with water, and the pH value was adjusted to 8.0.
[0041] The preparation method of buffer C is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 0.3mol sucrose with water to make up to 1 liter, adjust the pH value to 7.5.
[0042] The preparation method of buffer D is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 0.6mol sucrose with water to make up to 1 liter, and adjust the pH value to 8.0.
[0043] The preparation method of lysate is as follows: 0.01mol ...
Embodiment 2
[0058] Embodiment 2, the extraction of cotton mitochondrial DNA
[0059] 1. Solution preparation
[0060] The preparation method of buffer A is as follows: dilute 0.05mol Tris-HCl, 1.2mol NaCl, 2mmol EDTA, 6g polyvinylpyrrolidone (PVP), 2mmolβ-mercaptoethanol and 0.1g BSA to 1 liter with water, adjust the pH value to 7.5.
[0061] The preparation method of buffer B is as follows: 0.05mol Tris-HCl, 0.1mol sucrose, 0.01mol MgCl 2 and 1 g of polyvinylpyrrolidone (PVP) were adjusted to 1 liter with water, and the pH value was adjusted to 7.5.
[0062] The preparation method of buffer C is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 0.1mol sucrose with water to make up to 1 liter, adjust the pH value to 7.5.
[0063] The preparation method of buffer D is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 0.2mol sucrose with water to make up to 1 liter, and adjust the pH value to 7.5.
[0064] The preparation method of lysate is as follows: 0.01mol Tris-HCl, 0...
Embodiment 3
[0079] Embodiment 3, the extraction of cotton mitochondrial DNA
[0080] 1. Solution preparation
[0081] The preparation method of buffer A is as follows: dilute 0.05mol Tris-HCl, 1.2mol NaCl, 2mmol EDTA, 10g polyvinylpyrrolidone (PVP), 5mmolβ-mercaptoethanol and 0.8g BSA to 1 liter with water, adjust the pH value to 8.5.
[0082]The preparation method of buffer B is as follows: 0.05mol Tris-HCl, 0.5mol sucrose, 0.05mol MgCl 2 and 5 g of polyvinylpyrrolidone (PVP) were adjusted to 1 liter with water, and the pH value was adjusted to 8.5.
[0083] The preparation method of buffer C is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 0.5mol sucrose with water to make up to 1 liter, adjust the pH value to 7.5.
[0084] The preparation method of buffer D is as follows: mix 0.05mol Tris-HCl, 0.02mol EDTA-Na 2 and 1.0mol sucrose with water to make up to 1 liter, and adjust the pH value to 8.5.
[0085] The preparation method of lysate is as follows: 0.01mol Tris-HCl, 0...
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