http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2708561-T3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
filingDate 2014-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4bdeef1bc5ee28674a960b14e8dfabda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9e0695144ca7567391bfa4eb7328d58
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publicationDate 2019-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2708561-T3
titleOfInvention Methods for the purification of messenger RNA
abstract A method of purification of messenger RNA (mRNA), comprising (a) synthesizing mRNA by In Vitro transcription using the following reagents: (i) a linear or circular DNA template containing a promoter; (ii) a set of ribonucleoside triphosphates; (iii) a buffer system that optionally includes DTT and magnesium ions; and (iv) an RNA polymerase; and optionally (v) a DNase I, a pyrophosphatase and / or an RNAse inhibitor; (b) adding a protein denaturing agent to the preparation of step (a), which comprises the In Vitro synthesized mRNA, wherein the protein denaturing agent is a chaotropic agent or a high salt concentration; and (c) purifying the mRNA from the preparation of step (b) by tangential flow filtration, wherein the tangential flow filtration comprises: (i) a transmembrane pressure between 1 and 30 pounds per square inch; (ii) a feed rate between 50 and 500 mL / minute; (iii) a flow rate between 10 and 100 mL / minute; and (iv) a filter having a nominal molecular weight limit of between 200 kDa and 700 kDa, wherein the purified mRNA of step (c) contains undetectable levels of prematurely aborted RNA sequences and enzymatic reagents used in In Vitro synthesis as determined by agarose gel electrophoresis or chromatographic methods.
priorityDate 2013-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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