http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112226484-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_653c418e41edbb4e1ce8bc5e53e70cec
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-48
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-48
filingDate 2020-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a616f0763ff34c4808bd0cffcce02a42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_720510ba6dc4e8a1c7fe6616965f17d0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c81b783b5fe9704b5388c81d2ebaf34e
publicationDate 2021-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-112226484-A
titleOfInvention Fluorescent biosensor and detection method and application of β-glucotransferase
abstract The invention discloses a β-glucose transferase fluorescent biosensor, a detection method and application, including detection probe, endonuclease, exonuclease, helicase, polymerase, primer DNA and SYBR dye; the detection probe The needle is a hairpin structure formed by single-stranded DNA, the detection probe has a recognition site that can be recognized and cleaved by an endonuclease, the recognition site contains 5-hydroxymethylcytosine, and both ends of the single-stranded DNA are Modified with phosphate ester; after the detection probe is recognized and cut by endonuclease, it can be further cut by exonuclease; the helicase can unwind the stem of the hairpin structure; the primer DNA and the After the single-stranded DNA is complementary, double-stranded DNA is formed under the action of polymerase; the SYBR dye can specifically bind to the double-stranded DNA. The fluorescent biosensor provided by the invention has high sensitivity to β-glucose transferase, good specificity and short detection time.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114062672-A
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priorityDate 2020-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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