http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110791474-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-077
filingDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8c87e62901512b3bab440c0792d1719
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publicationDate 2020-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110791474-A
titleOfInvention A kind of isolation and in vitro culture method of nucleus pulposus cells
abstract The invention discloses a method for separating and culturing nucleus pulposus cells in vitro. When the nucleus pulposus cells are separated, blood stains and cartilage tissue should be cleaned up to obtain nucleus pulposus tissue, so as to prevent miscellaneous cells from affecting the adherence of nucleus pulposus cells and subsequent culture, and the digestive juice With collagenase I, the digestion process is milder, the cells and tissues after digestion are more active, and they are easy to adhere to the wall. The digestion is terminated with a mixture containing 20% fetal bovine serum and DPBS, and the obtained cells are not easy to adhere. The bottle is more uniform, and the reagents used are added with 1% penicillin/streptomycin to prevent the contamination of the sample itself or during collection and transportation; in vitro culture, add the placental mesenchymal stem cell culture supernatant lyophilized powder solution, the addition amount is 10-40 %, make up for the lack of growth factors in the medium, and promote the growth of nucleus pulposus cells; the cultured cells have a high survival rate, are easy to adhere to, and have good cell morphology and high and stable quality.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112061600-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113025567-A
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priorityDate 2019-11-22-04:00^^<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: 27.