http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106749554-B
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2760-16151 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2760-16251 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2710-14021 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N7-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-005 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N7-01 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-18 |
filingDate | 2017-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2021-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2021-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-106749554-B |
titleOfInvention | Purification method of influenza virus hemagglutinin protein |
abstract | The invention relates to a purification method of influenza virus hemagglutinin protein, which comprises the following steps: s1, expression of hemagglutinin protein and collection of cells; s2, cracking cells and collecting lysate; s3, carrying out continuous anion-cation exchange chromatography on the lysate. The purification method of the invention has the advantages of simple operation, rapid production, high product purity, correct protein conformation, short process period, high yield and easy linear amplification to production scale. The purified HA protein HAs high recovery rate, the purity is more than 95 percent, and the biological activity of the HA protein is kept. |
priorityDate | 2017-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 227.