Quadruple PCR detection kit for diagnosis FAdV/MDV/ALV/REV
A technology for detecting kits and viruses, applied in the field of molecular biology diagnosis of animal diseases in animal medicine, can solve problems such as unreported
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Embodiment 1
[0053] (1) Design and preparation of primers
[0054] With reference to the genome sequences of group I avian adenovirus, Marek's disease virus, chicken lymphocytic leukemia virus and avian reticuloendothelial hyperplasia virus published in GenBank, combined with the related virus gene sequences determined by our group for several years, DNAStar biological The software comprehensively analyzed and compared, and designed 8 primers for the above 4 virus genes. The sequences of the primers are as follows:
[0055] FADV-F upstream primer: 5'-ATGACTGCGCTTACTCCCGA-3';
[0056] FADV-R downstream primer: 5'-ACCCAGATAGTTGGTACC-3';
[0057] MDV-F upstream primer: 5'-CAGCTGCGTATTTTCCCCG-3';
[0058] MDV-R downstream primer: 5'-AATTACTTGGTCTTTAACC-3';
[0059] ALV-F upstream primer: 5'-TGTAGTGTTTATGCAATACTC-3';
[0060] ALV-R downstream primer: 5'-GGGTATGTTGGCTCCCTGCA-3';
[0061] REV-F upstream primer: 5'-AATGTGGGAGGGAGCTCCGG-3';
[0062] REV-R downstream primer: 5'-ACATTTTCCCTCATT...
Embodiment 2
[0072] (1) Design and preparation of primers
[0073] Same as Example 1.
[0074] (2) Treatment of tissue samples and extraction of DNA solution
[0075] 1) Take 3-5 g of tissue materials of suspected cases, such as enlarged liver and spleen, cut into paste, add 5 times sterile PBS, fully grind with a tissue grinder, collect the suspension, 4 ℃, 12 000 r / min Centrifuge for 10 min, aspirate the supernatant, and set aside.
[0076] 2) Pipette 100 μL of the supernatant of the suspected case tissue disease material into a 1.5 mL sterile EP tube, add 800 μL of lysis solution, invert and mix, let stand for lysis for 10 minutes, add 600 μL of ice-cold absolute ethanol, invert and mix, and let stand Precipitate for 10 min, centrifuge at 4°C, 12000 r / min for 10 min, discard the supernatant, wash once with 75% ethanol, discard the ethanol, invert the EP tube to air dry naturally, use 40 μL of 8 mmol·L -1 The NaOH solution was dissolved to obtain the DNA solution of the suspected case...
Embodiment 3
[0083] (1) Design and preparation of primers
[0084] Same as Example 1.
[0085] (2) Treatment of serum samples and extraction of DNA solution
[0086] 1) Collect blood from the fin vein of the chickens of the suspected case, coagulate naturally, and separate the serum after the serum is separated out for use.
[0087] 2) Pipette 100 μL of the serum to be tested and put it into a 1.5 mL sterile EP tube, add 800 μL of lysis solution, invert and mix, let stand for lysis for 10 min, add 600 μL of ice-cold absolute ethanol, invert and mix, let stand for 10 min, and settle at 4°C , Centrifuge at 12000 r / min for 10 min, discard the supernatant, wash once with 75% ethanol, discard the ethanol, invert the EP tube to air dry naturally, use 40 μL of 8 mmol·L -1 The NaOH solution was dissolved to obtain the DNA solution of the separated serum to be tested, which was used for later use.
[0088] 3) Simultaneously carry out the treatment of the negative control sample solution: draw 10...
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