http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002034559-A1

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-245
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P21-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-245
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02
filingDate 2001-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_498699a0e95cf13649a722df01edbc83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52113723b1fa1d930fe49df7f151cc0a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20eced650e7164854db7990f90243f1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccb4ebd8107c0bda5116abe95fb7b6e5
publicationDate 2002-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002034559-A1
titleOfInvention E. coli extract for protein synthesis
abstract There is now a market for kits containing the necessary components for performing protein synthesis reactions using template DNA of the experimenter. One category of existing system for performing protein synthesis reactions is based on an S-30 extract from the bacteria E. coli. It is disclosed here that a simple fractionation process can dramatically improve the performance of an S-30 prokaryotic protein synthesis reaction mixture. In one embodiment, the fractionation is a simple freezing and thawing of an S-30 extract combined with a supplemental mix, followed by centrifugation. The resulting fractionated S-30 reaction mixture yields more full-length target protein and less non-full length or non-target protein than possible using prior art S-30 systems.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7399620-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007218538-A1
priorityDate 2000-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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