http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113444772-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6806
filingDate 2021-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_576314bb0cf611fa93d59ee526d72073
publicationDate 2021-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113444772-A
titleOfInvention virus preservation solution
abstract The invention relates to the technical field of virus preservation, and discloses a virus preservation solution, including an inactivated type and a non-inactivated type. The main component of the inactivated type is guanidine isothiocyanate, and the main component of the non-inactivated type is Hank's balanced salt. Type also includes Triton 100, balanced salts, and EDTA chelating agent, wherein the quantity of guanidine isothiocyanate is 10-15 parts, the quantity of Triton 100 is 8-10 parts, and the quantity of balanced salts is 7-8 parts, The quantity of EDTA chelating agent is 5-8 parts, and the virus preservation solution is prepared by the above-mentioned components. The inactivated type preservation solution can directly lyse the virus to release single-stranded RNA and eliminate nucleic acid decomposition enzymes, so that the inactivated type can be used when it is used. The complete inactivation of the virus greatly improves the safety of scientific researchers in virus research, and at the same time, the preparation method of the inactivated preservation solution is simple, which is convenient for mass production and manufacture.
priorityDate 2021-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 30.