Use of SARS coronary virus ORF8 region
A coronavirus, ORF8 technology, applied in the field of virology and molecular epidemiology
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Embodiment 1
[0061] Preparation of SARS coronavirus genome typing detection kit
[0062] A kit is prepared which contains:
[0063] Name Sequence (5′→3′) Number Concentration
[0064] Forward primer atgaatgagc tcactttaat SEQ ID NO: 3 dry powder 2OD
[0065] Reverse primer ttaatttgtt cgtttatta SEQ ID NO: 4 dry powder 2OD
[0066] PCR reaction solution containing Taq enzyme dNTP magnesium ion PCR reaction buffer
Embodiment 2
[0068] Detection of infectivity and genome typing of SARS coronavirus
[0069] With the test kit in embodiment 1, three kinds of SARS coronavirus strains (blind method) to be tested carry out PCR amplification (please describe the detection process in a little detail), then sequence determination is carried out to the amplified product. The infectivity was determined according to whether the ORF8 region was missing.
[0070] The test results are consistent with the actual infectivity of the three SARS coronavirus strains (that is, the number of clinically infected people). In addition, the SARS coronavirus genotype determined based on the deletion is completely correct.
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