http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02242681-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44763f812307e730e61c30845b38c38f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-37
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-37
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
filingDate 1989-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b3dd64849ae12f7df3e9c50c987ed52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_262e886927da824004ceecd2d9eb2010
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publicationDate 1990-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02242681-A
titleOfInvention Aleuria aurantia lectin cdna and recombinant vector containing thereof
abstract PURPOSE: To efficiently produce fucose-specific lectin (Aleuria aurantia lectin, AAL) by transforming host cell with using recombinant vector coding Aleuria aurantia lectin or simulant of said lectin. n CONSTITUTION: Recombinant vector coding Aleuria aurantia lectin or simulant of said lectin and having manifestable region in host cell is used to transforma tion of host cell such as colibacillus. Next, said transformed colibacillus strain is cultured to mass produce fucose-specific AAL or simulant of said AAL. Produced AAL or simulant of said AAL is able to be purified by ammonium sulfate precipitation method or fucose.starch gel column chromatography, etc. Colibacillus Y 1090 strain is preferable as colibacillus as host cell. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017203762-A
priorityDate 1989-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 21.