http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008148625-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_aac831a6be8de686431c615fcce2d8ae |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-877 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-0735 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-07 |
| filingDate | 2006-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d3fd83590270e2db6b2dd137e8d5f92a |
| publicationDate | 2008-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2008148625-A |
| titleOfInvention | Clone ES cell production method |
| abstract | [PROBLEMS] To provide a human ES cell production technology capable of clearing ethical problems and a technology related to the production technology. A nucleus derived from a somatic cell is transplanted to an enucleated unfertilized egg to form a cloned embryo, and the cloned embryo is developed to a split embryo. After that, for example, the blastomere cells of the divided embryos generated up to the 8-cell stage are co-cultured with separately prepared ES cells of the same animal species, so that the cloned ES cells derived from the divided embryos, that is, the blastomere cell-derived clone ES cells. To produce. Thereafter, the clone ES cell is selected and cultured to establish a clone ES cell line. [Selection] Figure 1 |
| priorityDate | 2006-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 16.