http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002253270-A

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02
filingDate 2001-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a276f4aa9bdaf9b440424eea42f6e8e6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8038469391b9a585b8255f6835545bd9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36acfc4bf3791da221a54713a8c09098
publicationDate 2002-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002253270-A
titleOfInvention Method for producing recombinant protein
abstract (57) [Problem] To provide a method for efficiently producing a recombinant protein from which an N-terminal methionine has been removed. SOLUTION: In culturing a host transformed with an expression vector for expressing a recombinant protein, the concentration of dissolved oxygen in the culture solution is controlled to about 1 ppm or less. [Effect] By controlling the concentration of dissolved oxygen in the culture solution to be low, the expression ratio of the recombinant protein to which the N-terminal methionine is not added is increased as compared with the case where such control is not performed.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006129751-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2004058959-A1
priorityDate 2000-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 500.