Multiple-PCR primer system for quickly testing animal origin ingredients of pigs, sheep and cows and testing method
A technology of animal-derived components and detection methods, applied in the field of molecular biology, can solve the problems of single qualitative detection of animal-derived meat and meat products, incompetent detection technology, non-specific amplification, etc., and shorten the detection time. , shorten the experimental time, the effect of specific detection and analysis
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Embodiment 1
[0048] Embodiment 1 carries out PCR amplification with the primer pair I of pig 12SrRNA gene as primer
[0049] Taking the total DNA samples of each species as the total DNA template, the agarose gel electrophoresis pattern of the total DNA template is as follows: figure 1 shown. Depend on figure 1 It can be seen that the genomic DNA fragments extracted from various animal samples are uniform and the bands are clear, which provides a good template for the PCR reaction based on the nucleic acid level.
[0050] 1) Treatment of the total DNA samples of each species: the total DNA samples of 8 kinds of animals were diluted to 50 ng / μl as the total DNA template, and the primers were diluted to 10 μmol / L.
[0051] 2) Preparation of the reaction system: add the following reaction components into the PCR tube, the reaction system is 50 μl / tube. 36 μl of double distilled water, 5 μl of 10*PCR reaction buffer, 4 μl of 2.5 mM dNTPs, 2 μl of 2.5 U / μl Taq enzyme, 1 μl of total DNA templ...
Embodiment 2
[0055] Example 2 Carrying out PCR amplification with the primer pair II of sheep cytochromecoxidase subunit III gene as primers
[0056] 1) Treatment of the total DNA samples of each species: the total DNA samples of 8 kinds of animals were diluted to 50 ng / μl as the total DNA template, and the primers were diluted to 10 μmol / L.
[0057] 2) Preparation of the reaction system: add the following reaction components into the PCR tube, the reaction system is 50 μl / tube. Double distilled water 36 μl, 10*PCR reaction buffer 5 μl, 2.5 mM dNTPs 4 μl, 2.5 U / μl Taq enzyme 2 μl, total DNA template 1 μl, 10 μM forward primer of primer pair III 1 μl and 10 μM reverse primer of primer pair III 1 μl, where the Taq enzyme is a conventional Taq enzyme (refer to Tiangen Company’s Taq enzyme instructions).
[0058] 3) The formulation of the PCR reaction program: pre-denaturation at 95°C for 10min, denaturation at 94°C for 30s, annealing at 52°C for 45s, extension at 72°C for 90s, 35 cycles, ext...
Embodiment 3
[0061] Embodiment 3 carries out PCR amplification with the primer pair III of bovine TNFRSF10A gene as primer
[0062] 1) Treatment of the total DNA samples of each species: the total DNA samples of 8 kinds of animals were diluted to 50 ng / μl as the total DNA template, and the primers were diluted to 10 μmol / L.
[0063] 2) Preparation of the reaction system: add the following reaction components into the PCR tube, the reaction system is 50 μl / tube. Double distilled water 36 μl, 10*PCR reaction buffer 5 μl, 2.5 mM dNTPs 4 μl, 2.5 U / μl Taq enzyme 2 μl, total DNA template 1 μl, 10 μM forward primer of primer pair III 1 μl and 10 μM reverse primer of primer pair III 1 μl, where the Taq enzyme is a conventional Taq enzyme (refer to Tiangen Company’s Taq enzyme instructions).
[0064] 3) The formulation of the PCR reaction program: pre-denaturation at 95°C for 10min, denaturation at 94°C for 30s, annealing at 52°C for 45s, extension at 72°C for 90s, 35 cycles, extension at 72°C for...
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