http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010158256-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ee1c19da359446fb5c4f0458a57b783d
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
filingDate 2010-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8401dfc55e43cffb49981913685442c0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_711d90023e925a32b51c23969b0c3345
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b54cc780718c172351b956f3c88f643f
publicationDate 2010-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010158256-A
titleOfInvention Yeast transformation method
abstract The present invention provides a yeast transformation method that does not require adjustment of competent cells and can easily and easily treat a large number of strains. SOLUTION: It consists of a buffer solution containing DNA for transformation, carrier DNA, polyethylene glycol and lithium salt, 0.5 to 10 μg of DNA for transformation per 100 μL, and 20 times mass of carrier DNA relative to the DNA for transformation. 1 × 10 7 or more yeast cells cultured on SD solid medium are added to the treatment solution containing the above, and incubated at 25 to 35 ° C. for 30 minutes or more. A method for producing a transformant by transforming with a DNA for transformation. [Selection] Figure 1
priorityDate 2010-04-23-04:00^^<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: 24.