Primers for loop-mediated isothermal amplification of avian reoviruses, detection kit of avian reoviruses and detection method
An avian reovirus, ring-mediated isothermal technology, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc., to achieve the effects of high specificity and sensitivity, convenient observation and simple operation
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Embodiment 1
[0062] Embodiment 1, the preparation of avian reovirus detection kit
[0063] 1. Synthesis of primers
[0064] Artificially synthesize the following 3 pairs of primers, the outer primer pair:
[0065] Upstream primer F3: 5'- ATGCTGCGTATGCCTCCC-3',
[0066] Downstream primer B3: 5'-CCAGCTCACGATGGAAGAC-3',
[0067] Inner primer pair:
[0068] Upstream primer FIP:
[0069] 5'-ACGTAGCTTGCAAATCACCACCTTTTTGTGTAACGGTGCGACTGCT-3',
[0070] Downstream primer BIP:
[0071] 5'- CATAATTGCATATTGGCCTTATCTTTTTTACGTGCAGCGTCCGCCTT-3',
[0072] Circular primer pair:
[0073] Upstream primer LF: 5'- GCCTGACAATGAACGTTACC-3',
[0074] Downstream primer LB: 5'- AGCGGCGGGTGGTGGTTTC-3',
[0075] 2. Preparation of LAMP reaction solution
[0076] Each 24μL LAMP reaction solution contains the following components: 20mM Tris-HCl, 10mM KCl, 10mM (NH 4 ) 2 SO 4 , 4-16mM MgSO 4 , 0.1% Tween20, 0.05 mM Calcein, 0.6mM MnCl 2 , 0.2U AMV reverse transcriptase, 0.8M betaine, 1.4mM deoxynuc...
Embodiment 2
[0082] Get two chickens, one is diagnosed as a sick chicken infected with avian reovirus, and one is healthy. Two chickens were sampled separately with cloacal swabs. The detection kit prepared in Example 1 was used to detect the samples.
[0083] 1. Extraction of RNA
[0084] Collect the cloacal cotton swabs separately, rinse the cotton swabs repeatedly in a centrifuge tube with 0.2mol / L pH7.4 phosphate buffer solution, take out the cotton swabs, centrifuge at 500Orpm for 1min, and take the supernatant to obtain the test solution of 2 chickens.
[0085] The operation of extracting RNA is an existing technology, and only one of the specific operations is listed as follows, but it is not limited to this kind of operation:
[0086] Add 250 μL of detection solution and 750 μL TRIzol Reagent to a centrifuge tube, shake vigorously, and ice-bath for 5 minutes; add 200 μL of chloroform, and ice-bath for 5 minutes; centrifuge at 12,000 rpm for 10 minutes at 4°C, take the aqueous...
Embodiment 3
[0094] Get two chickens, one is diagnosed as a sick chicken infected with avian reovirus, and one is healthy. Two chickens were sampled separately with cloacal swabs. The detection kit prepared in Example 1 was used to detect the samples.
[0095] 1. Extraction of RNA
[0096] Same as Step 1 of Example 2.
[0097] 2. Loop-mediated isothermal amplification
[0098] Add 1 μL to each of the three reaction tubes containing 24 μL of the LAMP reaction solution to obtain the RNA sample of the diseased chicken in step 1, as the detection group 1; add 1 μL to each of the three reaction tubes containing 24 μL of the LAMP reaction solution. Get the RNA samples of healthy chickens as the detection group 2; add 1 μL positive control to each of the three reaction tubes containing 24 μL of LAMP reaction solution, as the positive control group;
[0099] 1 μL of sterilized double-distilled water was added to each reaction tube as a negative control group.
[0100] At the same time, the r...
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