Primer group and probe for building specific quantitative PCR (polymerase chain reaction) precise detection by transgenic maize MON88017 and method thereof
A technology of genetically modified corn and detection methods, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc., to achieve the effects of high amplification efficiency, scientific and reasonable detection methods, and protection of the right to know and the right to choose
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Embodiment 1
[0032] The quantitative detection in this embodiment adopts the 7500 fluorescent quantitative PCR instrument produced by ABI Company.
[0033] The construction of a specific quantitative PCR accurate detection method for transgenic maize MON88017 includes the following steps:
[0034] Step 1: Synthesize upstream primers, downstream primers and fluorescent probes used in conjunction with the primers,
[0035] Upstream primer sequence: Construct MON88017-Forward:
[0036] 5'-GGGCTTAGATGAGAAACTTCACGAT-3';
[0037] Downstream primer sequence: Construct MON88017-Reverse:
[0038] 5'-CCGACTCTCTTCTCAAGCATATGA-3';
[0039] Fluorescent probe sequence: Construct MON88017-Probe:
[0040] 5'-FAM-CGCGCCAAAGCTTACTCGAGGTCA-TAMARA-3'.
[0041] Wherein, the synthetic concentration of upstream primer, downstream primer and fluorescent probe is 10 μmol / l.
[0042] The nucleotide sequences of the above upstream primers, downstream primers and fluorescent probes are designed for a specific s...
Embodiment 2
[0050] Amplification efficiency experiment
[0051] The method data of this embodiment was continuously repeated to make 29 parallel samples, and the 29 samples were detected, and the detection data are shown in Table 1.
[0052] Table 1
[0053]
[0054]
[0055] The invention can accurately detect the specific DNA fragment and its content constructed by MON88017 in transgenic corn, obtain the slope of the standard curve, which is between -3.6 and -3.1, the correlation coefficient is greater than 0.99, and the amplification efficiency is 102.102%, which is 90% to 110%. In the range. The quantitative test result (1.6%) of the sample to be tested is very close to the true value (1.5%), the relative deviation (6.7%) of the test result is less than 25% internationally recognized, and the uncertainty of the test result is less than 10%.
[0056] The above results show that the present invention has good amplification efficiency.
Embodiment 3
[0058] Specific detection
[0059] Materials used to build specificity:
[0060] Transgenic corn: T25, MON810, Bt11, Bt176, GA21, TC1507, 59122, MON89788, NK603, MON863, BvLa;
[0061] Transgenic rice: KF6, KMD, TT51-1, TA2-1;
[0062] Genetically modified tobacco: TMV;
[0063] Transgenic sugar beet: H7-1;
[0064] Genetically modified soybean: GTS40-3-2;
[0065] Transgenic cotton: MON15985, LLC25, MON1531, MON88913, GHB614, MON1445;
[0066] Transgenic rapeseed: GT73, T45, MS8, RF1, RF2, RF3.MS1, MS8
[0067] The DNA of the above-mentioned samples was analyzed using the primer set and probe of the present invention.
[0068] The result is as figure 1 As shown, using the primer set and probe of the present invention to detect transgenic corn non-MON88017 varieties, transgenic rice, transgenic soybean, transgenic rape and non-transgenic corn, rice, rape, soybean (horizontal curve in the figure) and transgenic corn MON88017 strain test materials, Only the material of tra...
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