Nested fluorescent PCR detection primer, probe, kit and detection method of donkey-origin, horse-origin, swine-origin and bovine-origin in donkey-hide gelatin, and applications thereof
A technology for detecting primers and porcine origin, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc., and can solve problems such as DNA damage, linear genomic DNA fragmentation, inaccuracy
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Embodiment 1
[0089] DNA extraction based on donkey-hide gelatin samples: using the method disclosed in the patent 201410317118.7 (a kit for quickly extracting DNA from donkey-hide gelatin and its extraction method), the steps will not be repeated, and the purity of the extracted genomic DNA is determined by ultraviolet spectrophotometer and concentration. The measured OD260 / OD280 values are both about 1.8-1.9, and the concentration is above 10ng / μl, indicating that the DNA is of high purity and moderate concentration, which meets the requirements of PCR amplification.
[0090]1. Selection of target genes and design of primers: Compared with the genome, the copy number of mitochondria in tissues is higher, and the degree of damage of donkey-hide gelatin after deep processing is relatively small, so the mitochondrial 16SrDNA gene is preferred. The external primers and internal primers are designed for donkeys and pigs, and the amplified fragments are small, making it easier for the primers...
Embodiment 2
[0095] Example 2 Kit specificity verification
[0096] Using the detection kit provided by the present invention, the genomic DNA is extracted from animal skins or fresh tissues such as cattle, pigs, horses, donkeys, camels, yaks, goats, sheep, rabbits, fish, chickens, ducks, minks and foxes as templates, Perform multiple nested real-time fluorescent PCR detection according to the above method to verify the specificity of this kit. The test results are shown in Table 5. Only the genomic DNA of donkey, pig, horse and cow was detected, and the rest of the animal-derived DNA was not detected, indicating that the detection method of this kit has good specificity.
[0097] Table 3 Specificity Verification
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[0099]
Embodiment 3
[0100] Embodiment 3 Sensitivity experiment
[0101] Quantify donkey, pig, horse and bovine genomic DNA to 5×10 -2 ng / μl, 5pg / μl and 0.5pg / μl, 0.05pg / μl, 0.005pg / μl Each PCR reaction was added with different concentrations of donkey, horse, cow and pig DNA as a template, and the amount added was 2μl, that is, the DNA content 0.1ng, 0.01ng, 1pg, 0.1pg, 0.01pg respectively, amplified according to the above PCR system and detection method, the results are shown in Figure 8 to Figure 11 , as can be seen from the figure, the detection limit of the present invention is 0.1pg, and the detection sensitivity reaches the picogram level, which is 1000 times higher than that of ordinary nested PCR amplification.
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