RT-LAMP detection primers for Cyprinid Nidovirus HL39 (CyNV-HL39) and application thereof
A RT-LAMP, coronavirus technology, applied in the determination/inspection of microorganisms, DNA/RNA fragments, recombinant DNA technology, etc., can solve the problem of no detection method, and achieve simple result judgment, good sensitivity and good specificity Effect
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Embodiment 1
[0017] A carp coronavirus HL39, its isolation process is as follows:
[0018] 1) Take out and grind the virus-carrying carp liver, brain, spleen, kidney and other tissues, dilute the medium 100 times, centrifuge at 2000rpm, take the supernatant and filter, inoculate into grass carp ovary cell line (GCO) Monolayer, cultivated at 25°C for 7 days, resulting in cytopathic effect (CPE), it can be seen that GCO cells shrink and become round, the refractive index increases, some cells begin to fall off, and the cell monolayer begins to rupture. Medium: M199, 10% fetal bovine serum, pH 7.0~7.2;
[0019] 2) Collect diseased cells and conduct morphological identification using transmission electron microscopy: Morphological characteristics of carp coronavirus HL39: the virus is rod-shaped, with obvious coronal-shaped spine structures around it, which is consistent with the typical morphology of coronaviruses.
[0020] 3) The virus is collected, and its whole genome is sequenced, and th...
Embodiment 2
[0023] The RT-LAMP detection primers designed based on the difference between the full sequence of carp coronavirus HL39 (shown in SEQ ID NO.1) and the full sequence of other viruses are:
[0024] F3: 5'-TGCCCACCAAGACGACTA-3';
[0025] B3: 5'-TTTGCGCTAGCGCGATTC-3';
[0026] FIP: 5'-CGTTCCAAACGTCTTGGGTCAAGAGTGACGTAACTGCTACTG-3';
[0027] BIP: 5'-ACTCACTTCTGCTCCTTGCGACGCAGAGTGTAAGAGGTTTTTCCA-3'.
Embodiment 3
[0029] Utilize the RT-LAMP primer of carp coronavirus HL39 to detect CyNV-HL39, the method steps are as follows:
[0030] 1), the acquisition of viral RNA:
[0031] use or Total RNA was extracted by LS reagent or column adsorption and elution method.
[0032] 2), RT-LAMP amplification:
[0033] Use 25 μL reaction system: internal primers FIP and BIP each 0.8 μM, external primers F3 and B3 each 0.1 μM, dNTPs1 mM, Betaine0.5M, MgSO 4 5mM, Bst DNA polymerase 8U, AMV reverse transcriptase 5U, template RNA 5μL, 10×ThermoPolReaction Buffer 2.5μL, choose RT-LAMP reaction at 64℃ and 60min, then inactivate at 80℃ for 2min.
[0034] 3) To judge the test results, one of the following three methods is adopted:
[0035] A. When the amplification reaction occurs, the pyrophosphate ions precipitated from the dNTPs and the magnesium ions in the reaction solution form a white magnesium pyrophosphate precipitate. Judging by the naked eye: if the detection tube is obviously turbid, it is...
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