http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109507429-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6848
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filingDate 2018-02-14^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d646f88fee0448ce62c2787ea5dc0a65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2e9b09b92a47181bf6fcd32edea6e69
publicationDate 2019-03-22^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109507429-A
titleOfInvention A method for the identification and analysis of site-specific interacting proteins based on CRISPR/cas9 and peroxidase APEX2 systems
abstract The invention belongs to the field of biotechnology, and relates to a method for identifying and analyzing specific site-interacting proteins based on CRISPR/cas9 and peroxidase APEX2 systems, including steps, transformation of plasmids; Biotin labeling; detection and analysis of biotin-labeled protein complexes and enriched proteins using streptomycin magnetic beads. The experimental analysis results show that this method is suitable for the research and analysis of proteins at any given chromosomal location; at the same time, the idea of combining the CRISPR gene editing system with APEX2 for site-specific protein analysis is also applicable to other genome editing methods ( such as TALEN) binding to APEX2. The method is simple in operation, high in sensitivity, high in specificity, and good in reproducibility, and is suitable for studying chromatin local interacting proteins at any given chromosomal location.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110702916-A
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priorityDate 2018-02-14^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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