http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0830059-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N3-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N1-02
filingDate 1996-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f60d998d65922b52985747f4bd6e400
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e54610f411dc3f6d026ee6c3cd3af46a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8113dd921a1662c0a28f2c8410434e6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e93756ad78ce6bcc1404859c647f5e07
publicationDate 1998-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0830059-A2
titleOfInvention Cryopreservation of diverse plant cells
abstract The present invention relates to methods for cryopreserving plant cells and to methods for recovering viable plant cells from long or short term cryopreservation. Plant cells to be cryopreserved can be grown in culture and pretreated with a solution containing an cryoprotective agent and, optionally, a stabilizer. Stabilizers are preferably membrane stabilizers such as ethylene inhibitors, oxygen radical scavengers and divalent cations. Cells can also be stabilized by subjecting the culture to a heat shock. Pretreated cells are acclimated to a reduced temperature and loaded with a cryoprotective agent such as DMSO, propylene glycol or polyethylene glycol. Loaded cells are incubated with a vitrification solution which, for example, comprises a solution with a high concentration of the cryoprotective agent. Vitrified cells retain less than about 20% water content and can be frozen at cryopreservation temperatures for long periods of time without significantly altering the genotypic or phenotypic character of the cells. Plant cells may also be cryopreserved by lyophilizing cells prior to exposure to a vitrification solution. The combination of lyophilization and vitrification removes about 80% to about 95% of the plant cell's water. Cells can be successfully cryopreserved for long periods of time and viably recovered. The invention also relates to methods for the recovery of viable plant cells from cryopreservation. Cells are thawed to about room temperature and incubated in medium containing a cryoprotective agent and a stabilizer. The cryoprotective agent is removed and the cells successfully incubated and recovered in liquid or semi-solid growth medium. The invention also relates to the cryopreserved cells and to viable plant cells which have been recovered from long or short term cryopreservation.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8338143-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11350583-B2
priorityDate 1995-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399383
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128555702
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129001657
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID938
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399382
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226405992
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54676860
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15008977
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87143477
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID99806
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1144434

Total number of triples: 308.