Nest-type fluorescence PCR detection primers, probe composition and kit for donkey and pig-sourced ingredients in colla corii asini and detection method and application
A technology for detecting primers and porcine origin, applied in biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., can solve problems such as easy contamination, linear genomic DNA fragmentation, and difficulty in successfully amplifying large fragments. Achieve the effect of improving detection sensitivity, high degree of DNA damage, and improving amplification efficiency
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Embodiment 1
[0079] 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. Determination of OD 260 / OD 280 The values are all 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. .
[0080] 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...
Embodiment 2
[0085] Example 2 Kit Specificity Verification
[0086]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 3. Only donkey and pig genomic DNA were detected, and the rest of the animal-derived DNA was not detected, indicating that the detection method of this kit has good specificity.
[0087] Table 3 specificity verification
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Embodiment 3
[0090] Embodiment 3 Sensitivity experiment
[0091] Quantify donkey and pig genomic DNA to 5×10 -2 ng / μl, 5pg / μl and 0.5pg / μl, 0.05pg / μl, 0.005pg / μl were added to each PCR reaction with different concentrations of donkey and pig DNA as templates, and the amount added was 2μl, that is, the DNA content was 0.1ng , 0.01ng, 1pg, 0.1pg, 0.01pg, amplified according to the above PCR system and detection method, the results are shown in Figure 4 and Figure 5 , 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 other detection sensitivities.
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