http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104892734-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2770-32151 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2770-32134 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-09 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-09 |
| filingDate | 2015-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104892734-B |
| titleOfInvention | The method of hydrophobic interaction chromatography purification aftosa inactivation of viruses antigen |
| abstract | The method that the present invention relates to a kind of to purify aftosa inactivation of viruses antigen from cell culture fluid.The interaction between the hydrophobic grouping on hydrophobic grouping and hydrophobic interaction chromatography filler that this method passes through foot and mouth disease virus surface, by aftosa inactivation of viruses Antigen adsorption on chromatographic column, to be separated with the impurity in solution.The aftosa inactivation of viruses antigen being adsorbed on chromatographic column can be eluted using mild elution requirement, achieve the purpose that purification.This method speed is fast, and operating procedure is few, process stabilizing, aftosa inactivation of viruses antigen high income, and is easy to amplification and industrial-scale production, has biggish practical application value. |
| priorityDate | 2015-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.