Detection and identification kit of composite PCR of wheat stripe rust fungus and leaf rust fungus
A wheat stripe rust and kit technology, which is applied in the direction of microbial determination/inspection, biochemical equipment and methods, etc., can solve the problems of PCR and other problems in detecting and distinguishing between wheat stripe rust and leaf rust, and achieves strong specificity, The experimental operation is simple and the operation is simple and fast.
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Embodiment 1
[0042] Example 1 Composite PCR detection of susceptible wheat leaves and urediospores of rust fungus and its specificity analysis.
[0043] ①Mingxian 169 wheat seedlings were inoculated with wheat leaf rust 07-24-17 and stripe rust S23 alone or mixed in the artificial climate chamber, and the diseased leaves were collected 7 days later to extract genomic DNA; cultivate and collect 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.
[0044] ② Establish PCR reaction system
[0045] 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 template DNA (20ng / μl), and cover the PCR thin-walled reaction t...
Embodiment 2
[0050] The mensuration of embodiment 2 wheat rust composite PCR detection sensitivity
[0051] ① Gradually dilute the ureterospore DNA of leaf rust 07-24-3 and stripe rust S23 to the final concentration of 1.00pg / uL, 5.00pg / uL, 50.00pg / uL, 1.00ng / uL, 20.00ng / uL 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 final concentrations of 5.00pg / uL, 50.00pg / uL, 1.00ng / uL, 10.00ng / uL, 20.00ng / uL and 50.00ng / uL.
[0052] ② Establish PCR reaction system
[0053] 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.
[0054] ③PCR amplification
[0055] 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 ann...
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