http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103229721-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_810a8703d21e88e629b3b6753b1b79fe
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01H4-00
filingDate 2013-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c34de1031a2789e72c3321168804c09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_814bdc1b52f3c23ec2efcdee02067955
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6f1073c4c402ff10c68e050ce232966
publicationDate 2014-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103229721-B
titleOfInvention Tissue culture propagation method of Gynura formosana
abstract The invention provides a tissue culture propagation method of Gynura formosana. The method comprises the following steps of: with the stem of Gynura formosana as an explant, carrying out sterilizing, grafting and inducing operations to form callus; then, forming an integral plant seedling through proliferation of callus, bud induction and root induction; transplanting the integral plant seedling to a culture medium so that the integral plant seedling grows up inti normal Gynura formosana plant, wherein the basic culture medium is based on MS culture medium and assisted with components such as L-proline, 6-benzyladenine, 2, 4-dichlorphenoxyacetic acid, naphthylacetic acid, cane sugar, active carbon and the like. The method provided by the invention overcomes the problem of long culturing period and low propagation coefficient of Gynura formosana by using tissue culture, and industrial quick seedling can be performed, so that the method meets demand on Gynura formosana in market.
priorityDate 2013-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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