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filingDate 2001-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_528124feb036d4ebd7e93b70d3edfe05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8096eb718df4cad70d1894bdf7d975e8
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publicationDate 2003-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2003070465-A
titleOfInvention Schwann cell culture method
abstract [PROBLEMS] To provide a Schwann cell culture method capable of efficiently obtaining a large amount of Schwann cells. SOLUTION: 5-15% of peripheral nerve pieces treated with an enzyme After culturing in FCS-containing BS medium for 0-60 hours, culturing in serum-free BS medium for 12-60 hours to induce migration of Schwann cells under inhibition of fibroblast proliferation, then 1-10% FCS The cells are cultured in the BS medium for 7 days or longer, and Schwann cells are grown under the growth control of fibroblasts. In addition, after culturing in the above serum-free BS medium, peripheral nerve pieces taken out of the system were treated with serum-free BS medium and FCS. Schwann cells can also be grown by sequentially culturing in the BS medium containing. Furthermore, when Schwann cells are cultured on a bioabsorbable sheet, a cultured Schwann cell regeneration material is obtained.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101066472-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011013806-A1
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type http://data.epo.org/linked-data/def/patent/Publication

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