Nucleic acid composition and kit for detecting S gene of novel coronavirus and production method of kit
A nucleic acid composition and coronavirus technology, applied in the field of in vitro nucleic acid detection of viruses, can solve the problems of missed detection, hidden dangers of epidemic prevention and control, false negatives of nucleic acid detection kits, etc., and achieve the effect of improving accuracy and reducing the probability of occurrence
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preparation example 1
[0051] A novel coronavirus S gene detection nucleic acid composition:
[0052] Through the Global Influenza Sequence Database (GISAID) (www.gisaid.org), obtain the published whole genome sequence of the new coronavirus and the whole genome sequence of other 6 coronaviruses, and online (http: / / www.ebi.ac) .uk / ) Perform sequence comparison analysis on the gene sequence of 2 new coronaviruses and 6 other coronaviruses, and find the specific conservative sequence S gene on the whole genome sequence of the new coronavirus. The base sequence of this gene fragment is shown in the sequence table. As shown in SEQ ID NO. 4, S gene is used as the indicator gene, and a conservative sequence is selected as the target gene to be amplified on the S gene sequence. The base sequence of the conservative sequence is as SEQ ID NO. 5 in the sequence table. As shown, using real-time TaqMan fluorescent quantitative PCR design software BeaconDesigner7.0, for the target gene on the S gene, design a forwa...
preparation example 2
[0058] Positive control substance:
[0059] The recombinant plasmid DNA of pUC57-T containing the target gene SEQ ID NO.5 was constructed, and the recombinant plasmid DNA was used to transform E. coli DH5α competent cells, which were purchased from Beijing Soleibao Technology Co., Ltd. After the proliferation of Escherichia coli DH5α, the DNA was extracted by alkaline lysis, purified by DNA purification kit, and the A of the extracted DNA was measured with a spectrophotometer. 260 , A 280 And the concentration, the pseudovirus particles were obtained as a positive control.
Embodiment 1
[0061] A novel coronavirus S gene detection kit, which contains liquid forward primers, reverse primers, probes, DNA polymerase, reverse transcriptase, Tris-HCl, cations, dNTPs, RNase inhibitors and positive controls The forward primer, reverse primer and probe are prepared in Preparation Example 1, and the positive control product is prepared in Preparation Example 2. Forward primers, reverse primers, probes and positive controls are packaged separately.
[0062] The DNA polymerase is a hot-start Taq enzyme, and the reverse transcriptase is selected from one of c-MMLV reverse transcriptase or AMV reverse transcriptase, preferably c-MMLV reverse transcriptase. The RNase inhibitor is RNasin. The hot-start Taq enzyme, c-MMLV reverse transcriptase and RNasin can be packaged separately or at least two types can be mixed. In this embodiment, the hot-start Taq enzyme, c-MMLV reverse transcriptase and RNasin are in accordance with the table The final concentration in 2 is mixed as a pa...
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