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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a3dd4e2ea4af5781c0702795ef3ee0e1
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61L2202-21
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61L2-0088
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filingDate 2019-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8709701ee67d093eeba9e8dd2acf8693
publicationDate 2020-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-112121206-A
titleOfInvention A kind of virus inactivation method of human placenta extract
abstract The invention discloses a virus inactivation method for a human placenta extract, including the following steps: 1) using Trizol RNA extraction reagent to extract total RNA of bovine pancreas; 2) RT-PCR amplification of the total RNA of bovine pancreas 3) Cloning to prepare the expression bacteria of bovine ribonuclease A; 4) immobilization of bovine ribonuclease A; 5) enzymatic inactivation of virus in placenta extract. The method of the invention adopts genetic engineering technology, clones and expresses RNase efficiently, and immobilizes the RNase, so that the placenta extract is passed through the immobilized RNase, so that the nucleic acid of the virus particles in the placenta extract is specifically enzymatically hydrolyzed and lost. The method of the invention has the advantages of high efficiency, high selectivity, mild catalytic reaction conditions, no pollution, low cost, easy operation, the enzyme can be reused repeatedly, and the product is single.
priorityDate 2019-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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