http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1074139-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fdba90cf2180038389fe54d9614d0934 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_240c46550441bc0479a24ed73d829c8d |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-1007 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-22 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-00 |
| filingDate | 1982-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1984-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e850380cca965d11b962dd89fa087bd9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b26671c10b138f6d26968e9fb2c3b2b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_903e513d9e0d36d76a464d43cf3f204a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1f24de43b1c1f779987a7d88ca01e02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e37129b54ac6d02b818ab086749ed897 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc9d0e9a3e3c45a0a97787e610a8069b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6552023c4eaeb8187f40993fe2d3d465 |
| publicationDate | 1984-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SU-1074139-A1 |
| titleOfInvention | Method of constructing recombined plasma desoxyribonucleic acid and strain as producer of restriction endonuclease |
| abstract | 1. A method for constructing a recombinant DNA gshazmidnoy pIL RV8, comprising the steps that include Escherichia coli clones VKM B-1450 D PILRV7 with plasmid DNA clones containing truncated 500-600 bp pILRV7 A plasmid DNA having restriction and modification genes Eco -RV and having a unique restriction endonuclease site, then the plasmid PILRV7 DNA to the Phage c 1 875 DNA is treated with the Bg II restriction endonuclease, the fragments are stitched with the DNA ligase of phage T4, and transformed with the mixture of recombinant DNA molecules cells of Escherichia coll JC 5183 and from clones resistant to ampicillin and having immunitev including phage X vdel dissolved target recombinant plasmid DNA. . 2. Escherichia coli strain VKM B -1455 D (All-collection of Microorganisms with IBPM of the Academy of Sciences of the USSR) 8th producer of the endonuclease restriction ECORV. four; JI; o |
| priorityDate | 1982-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 60.