http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103290126-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6a92abd1ab31a1ccd759e3b4d41153ee |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01H1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 |
| filingDate | 2013-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31f217a49f08a84d355ad7da720353fa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f596cb3d891a611644df0e9eaf367105 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4417b0130d36e5e61e5b4effa3ea224d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9a38854fd1b7f4cd52902fe88ece394 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6b8691177514b7aa3f69359f404fa86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4a51143563fd1e5189983ef59509cd7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b179d40ec30f028c1677c40009eed1da http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f94483cc0b4fa29b9468d9ffcd4e2e56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70af3074cf910177e5baccc26f653818 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58f99517735e6ae73816bf00bbcacc3d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4629ee1c774e83e37d13a3af3f3d2636 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7498d9ad2bc2dc37f8aad42bd6867f3d |
| publicationDate | 2014-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103290126-B |
| titleOfInvention | Molecular marker for distinguishing cabbage eIF (iso) 4G gene wild type and mutant and application thereof |
| abstract | The invention discloses a site-specific dominant ASM marker for distinguishing cabbage eIF (iso) 4G wild type and a mutant, the marker which is related to wild type site detection is named as ASM-I4E. G, the fragment size is 1526bp, and the marker is as shown in SEQ (sequence) ID (identity) No. 1. Primers for identifying the specific dominant molecular marker are as follows: the forward primer PF1 is as follows: 5'-TTTTTTGGTTGTTGGAGATTTTG-3'; the reverse primer PR1 is as follows: 5'-GGTACTTCAGCTTTGACGAGGAC-3'; and the primers are as shown in SEQ ID No. 2 and SEQ ID No. 3. The marker can be applied to cabbage species resource identification and breeding assisted selection: a pair of primers of the ASM marker can be utilized for performing PCR (polymerase chain reaction) amplification on DNA (deoxyribonucleic acid) of a genome of an individual to be tested so as to detect whether an amplification fragment exists or not, if a ribbon can be amplified, the individual is of a homozygous wild type or a heterozygote, and if the ribbon can not be amplified, the individual is of a mutant type. According to the application disclosed by the invention, the screening means can be greatly simplified, the transferring years can be shortened, and the blindness in selection of a conventional breeding method can be avoided. |
| priorityDate | 2013-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 85.