http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110358812-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_29cbe62865e3313705e84bb43bde1877
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858
filingDate 2019-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3c0eb67d61a001234526c6264fdde8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d806ebac1ed23322051f899cd58e0de6
publicationDate 2019-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110358812-A
titleOfInvention A kind of primer and detection method for detecting positive clones of gene knockout and recombination in λ-Red recombination system
abstract The invention discloses a primer and a detection method for detecting positive clones of gene knockout and recombination in λ-Red recombination system. It belongs to the field of biotechnology engineering. The invention provides a universal detection primer, the design method of which is to design a pair of complementary primers at about 1/3 in the middle of the tetracycline tet RA gene, and use them in combination with the original identification primers for detection of recombination positive, respectively for detection of tet RA. The tetracycline gene tetRA is the 3'-end sequence and 5'-end sequence of the λ-Red recombination system knockout recombination positive clone of the replacement gene. The detection primers are designed in this way, so that there are three options for detecting recombinant positive clones, which can completely avoid the difficulty in judging positive results caused by the small difference between the sequence to be knocked out and the tetracycline tetRA gene. Moreover, the use of universal primers to detect recombination-positive clones can more effectively prove the correctness of the insertion position of the tetracycline tetRA gene.
priorityDate 2019-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005273869-A1
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP04635
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ93MW7
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5HKP6
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456490784
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9VG48
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ55EU1
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419533562
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54675776
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422501675
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO59952
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP61872
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA0A3Q1M1X5
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0C0R4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP61871
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP26504
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0C0R3
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423512670
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ3UT41
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA8WGN9
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP19515
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ20449
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCD4A9L7
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7567
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5U780
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP41773

Total number of triples: 38.