Degenerate reverse transcription-polymerase chain reaction (RT-PCR) detection reagent and kit for hantavirus group
A RT-PCR and hantavirus technology, applied in the field of hantavirus detection, can solve the problems of inevitable introduction, public reports, and inability to detect other viruses of hantavirus, so as to improve specificity and high sensitivity , good effect of specificity
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Embodiment 1
[0013] Embodiment 1, RT-PCR detection reagent and kit detect Hantaan virus
[0014] 1. Total RNA extraction: Vero cells were cultured with 5% inactivated calf serum DMEM at 37°C, routinely digested and subcultured into a monolayer, and then inoculated with Hantavirus 76-118 strains (Hantan type, courtesy of Zhejiang Center for Disease Control and Prevention) ), after 2 hours of adsorption, use 0.5% calf serum DMEM (purchased from Hyclone) to maintain the solution and place it at 37°C, CO 2 Cultured in an incubator. After 7-10 days of positive IFA detection, the cells were harvested and the total RNA of the cells was extracted with an RNA extraction kit (purchased from Qiagen) as positive RNA (the specific extraction method was in accordance with the instructions). Use a micro-spectrophotometer to measure the RNA concentration and purity, OD260 / 280≥1.9, indicating that the RNA is of high purity without DNA and protein contamination, take 50ng for RT-PCR reaction;
[0015] 2. ...
Embodiment 2
[0020] The actual detection of embodiment 2, RT-PCR detection reagent and kit to mouse Hantavirus
[0021] 253 mice collected in Daxie Port Area from 2008 to 2009 were killed by cervical dislocation after ether anesthesia, and 10-25 mg of lung tissue was collected, homogenized and extracted with RNA extraction kit for total RNA from lung tissue (specific extraction method According to the instructions), measure the RNA concentration and purity with a micro-spectrophotometer, OD260 / 280≥1.9, indicating that the RNA purity is high, without DNA and protein contamination, take 50ng for RT-PCR reaction; then proceed according to step 2 of Example 1 RNA reverse transcription, step 3 for PCR reaction, and step 4 for agarose gel electrophoresis, the results showed that 253 mouse lung samples were detected, and 2 of them were amplified to obtain bands of 478bp fragments. The test results were consistent with the results of the "National Detection Program for Hemorrhagic Fever with Renal...
Embodiment 3
[0022] Embodiment 3, RT-PCR detection reagent and kit detection detect Seoul type virus
[0023] It is basically the same as steps 1-4 of Example 1, except that the Hantavirus 80-39 strain virus (Seoul type, gifted by Zhejiang Center for Disease Control and Prevention) was inoculated, and the Hantavirus 80-39 strain Vero cells were detected A band with a size of 478 bp appeared in the culture, and the sequence of the sequencing result is shown in SEQ ID NO:5.
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