LAMP primer composition, kit and detection method for detecting pythium ultimum
The technology of primer composition and detection method is applied in biochemical equipment and methods, recombinant DNA technology, determination/inspection of microorganisms, etc. High accuracy and the effect of improving the reaction rate
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Embodiment 1
[0027] Embodiment 1: Utilize LAMP method to detect Pythium ultima
[0028] LAMP primer composition for detecting Pythium ultima: the forward inner primer FIP is shown in SEQ ID NO.1, the reverse inner primer BIP is shown in SEQ ID NO.2, and the forward outer primer F3 is shown in SEQ ID NO. 3, the reverse outer primer B3 is shown in SEQ ID NO.4, and the forward loop primer LF is shown in SEQ ID NO.5.
[0029] The concentration of each reagent in the LAMP kit for detecting Pythium ultima is: 1.6 μM forward inner primer FIP, 1.6 μM reverse inner primer BIP, 0.2 μM forward outer primer F3, 0.2 μM reverse outer primer B3, 0.8 μM forward Loop primer LF, 0.8M betaine, 1.4mM dNTPs, 20mM Tris-HCl, 10mM KCl, 10mM (NH 4 ) 2 SO 4 , 8mM MgSO 4 , 0.1% Triton X-100, Bst DNA polymerase 320U / ml, 2.4mM Hydroxynapthol Blue (HNB), and use ultrapure water to prepare 1mL detection solution.
[0030] LAMP detection method: extract the DNA of the microorganism to be tested, take 2 μL of the DNA...
Embodiment 2
[0032] Embodiment 2: the sensitivity test of Pythium ultima LAMP reaction
[0033] In order to determine the sensitivity of the LAMP detection method, the DNA concentration of the extracted Pythium ultima was measured with a spectrophotometer and then diluted 10 times. The DNA concentration range was set at 100ng-10fg, and 2 μL of the diluted DNA dilutions of each concentration were taken as Template, add 23 μL kit solution to carry out LAMP reaction, the reaction program is: 64 ° C reaction amplification for 60 min. HNB chromogenic reaction shows: when the DNA concentration of ultimate Pythium reaches 100pg, the solution in the reaction tube just can turn sky blue, further obtains the result consistent with HNB chromogenic reaction by agarose gel electrophoresis ( figure 2 ).
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