http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104611457-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6806 |
| filingDate | 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2019-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104611457-B |
| titleOfInvention | Arm-PCR primer design method for multiple target point gene magnification |
| abstract | The invention discloses a kind of Arm-PCR primer design methods for multiple target point gene magnification, through the following steps that realize: a, the primer that icubate2.0 online software design small fragment target gene is replaced with LAMP software；B, the cyclic primer sequence before inner primer that LAMP software design goes out is changed the universal linker sequence of Arm-PCR primer into；C, the preparation of Arm-PCR reaction system；D, the setting and operation of Arm-PCR reaction condition；E, the capillary electrophoresis detection of Arm-PCR product.The present invention is more using the primer sets that LAMP software design goes out, be conducive to the screening of multi-primers group, the present invention is used for the Arm-PCR primer design method of multiple target point gene magnification, it can enable the Arm-PCR primer successful design of small fragment target gene, and then Arm-PCR multiple reaction is made to become simple possible. |
| priorityDate | 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 19.