http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103627805-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b564e3ce0542c9d4e7813f6b3d2e4f19 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6851 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2013-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e63fd529a132a5adbf5ce32558f4388 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72f0995abbd1cf42a08374304d01596d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9469dd6ad68a53fb62f6fb097612ba2a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a600edc123b34d0ae80af7bf9bea4a86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25c9f7f0126701733527f98113268db9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30336a3ca2cc06f767c174a7ad60b07a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed08a8710c8e003d15678f1497592c4a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_181c29a94e5eabafa472b02e41be1d8a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ca9d8045260bcde35536a210448a07a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1f9ebfbc2ff6ae8b7edb61de5111eef |
| publicationDate | 2015-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103627805-B |
| titleOfInvention | Method for rapidly detecting industrial saccharomyces pastorianus higher alcohol metabolizing genes |
| abstract | The invention relates to biotechnologies and particularly relates to a method for rapidly detecting industrial saccharomyces pastorianus higher alcohol metabolizing genes. The method comprises the following steps: extracting RNA, preparing a cDNA template through reverse transcription reaction, performing multiple PCR, performing electrophoresis on blood capillaries, analyzing product segments, and metabolizing related genes BAP2-Sc, BAP2-Sb, BAT1-Sc, BAT1-Sb, BAT2-Sc and BAT2-Sb for the industrial saccharomyces pastorianus higher alcohol. According the invention, the GeXP multiple-gene expression quantitative analysis technology is adopted, compared with the conventional gene expression quantitative analysis technology (fluorescent quantitative PCR), the GeXP multiple-gene expression quantitative analysis technology has the characteristics of relatively strong specificity and sensitivity, and high degree of automation, so that the reliability and repeatability of results are ensured, and the experimental period is shortened greatly. The metabolism and content of higher alcohol are controlled during the process of fermentation under such condition that beneficial to different productions, and the typical tastiness and uniformity of beer are improved; product features are highlighted and new products are developed by rapidly regulating tastiness of the higher alcohol in the beer. |
| priorityDate | 2013-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 132.