Compound pcr detection and identification kit for wheat stripe rust and leaf rust
A technology of wheat stripe rust and kit, which is applied in the field of biotechnology, crop disease control and plant quarantine, can solve the problem of no detection and differentiation of wheat stripe rust and leaf rust by PCR, etc., and achieves strong specificity and simple experimental operation , Easy and fast operation
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Embodiment 1
[0045] Example 1 Multiplex PCR detection of susceptible wheat leaves and urediospores of rust fungus and its specificity analysis.
[0046] ①In the artificial climate chamber, wheat leaf rust 07-24-17 and stripe rust S23 were used to inoculate Mingxian 169 wheat seedlings alone or mixed, and the diseased leaves were collected 7 days later to extract genomic DNA; culturing and collecting wheat leaf rust (07- 24-17, 07-18-7, 07-24-3), stripe rust (S23, 07-6-3-11), uredospores of stem rust, and gibberella, powdery mildew, sheath blight, leaf blight Genomic DNA was extracted from the mycelia of , root rot, light fishy, and dwarf bacterium, and prepared as a 20ng / μl amplification reaction template.
[0047] ② Establish PCR reaction system
[0048] Take out the PCR-SMART reaction solution, melt at room temperature, mix well, add 7.5 μl to each PCR thin-walled reaction tube; then add 0.5 μl Taq enzyme, 16 μl ddH 2O. 1 μl template DNA (20ng / μl), and cover the PCR thin-walled react...
Embodiment 2
[0053] Example 2 Determination of Sensitivity of Detection of Wheat Rust Composite PCR
[0054] ① Gradually dilute the ureterospore DNA of Phyllostachys 07-24-3 and P. uL and 50.00ng / uL; Equal amounts of urediospore DNA of leaf rust 07-24-3 and stripe rust S23 were mixed and serially diluted to the final concentrations of 5.00pg / uL, 50.00pg / uL, 1.00ng / uL, 10.00ng / uL, 20.00ng / uL and 50.00ng / uL.
[0055] ② Establish PCR reaction system
[0056] Take out the PCR-SMART reaction solution, melt at room temperature, mix well, add 7.5 μl to each PCR thin-walled reaction tube; then add 0.5 μl Taq enzyme, 16 μl ddH 2 O. 1 μl of template DNA, and cover the PCR thin-walled reaction tube.
[0057] ③PCR amplification
[0058] Place the PCR thin-walled reaction tube in the PCR machine, and set the PCR reaction program: 94°C pre-denaturation for 5 minutes, 1 cycle; 94°C denaturation for 30S, 55°C annealing for 30S, 72°C extension for 40S, 35 cycles; 72°C extension 5min 1 cycle.
[0059]...
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