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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01K2227-105
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01K2267-0331
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2509-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N5-0693
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01K67-027
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filingDate 2020-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-112481215-B
titleOfInvention A stable and efficient PDX tumor model modeling method
abstract The invention discloses a stable and efficient PDX tumor model modeling method, which is characterized in that it comprises: preparing a balanced salt solution, and collecting tumor tissue, and the collected tumor tissue is stored in the balanced salt solution; The balanced salt solution comprises: HBSS, DMEM/F12 with a volume fraction of 10%, and penicillin and streptomycin with a mass fraction of 1%; the components and final concentrations of the HBSS are: NaCl, 140mM; KCl, 5mM; CaCl 2 , 1 mM; MgSO 4 ·7H 2 O, 0.4 mM; MgCl 2 ·6H 2 O, 0.5 mM; Na 2 HPO 4 , 0.3 mM; KH 2 PO 4 , 0.3 mM; both glucose and NaHCO 3 4 mM; 10% fetal bovine serum. The PDX tumor model modeling method of the present invention is stable and efficient, and has a high success rate.
priorityDate 2020-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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