http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1648978-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_de155c83138a355d47f1ed44dd90894e |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04 |
| filingDate | 1989-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1991-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a935667b3caae1be1011917f7e1ed11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cbd0b61585489f1a85832e6d834324ca |
| publicationDate | 1991-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SU-1648978-A1 |
| titleOfInvention | Method of detection of escherichia virulence |
| abstract | This invention relates to medical microbiology and concerns the detection of the virulence of Escherichia. The purpose of the invention is to improve the accuracy of the method. The isolated strains of pathogenic Escherichia are seeded in sectors of 6-8 strains per dish with m seppepton agar, incubated in a thermostat at 37 ± 0.2 ° C for 16-20 hours. pipette 4-5 cm of the azureosin solution according to Romanovsky, additionally diluted with V10 distilled water. After 1-2 minutes, the paint is drained and take into account the presence of dark blue or black staining for the growth of virulent strains. The method gives the same results with the methods H1y, CFA, CCP (respectively, hemolysis in the medium with 5% of red blood cells, d-mannose-resistant hemagglutmism, keratoconjunctival sample). 1 tab |
| priorityDate | 1989-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID161658 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419574941 |
Total number of triples: 14.