http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20220073327-A

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filingDate 2020-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2022-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20220073327-A
titleOfInvention Primer set for multiplex loop-mediated isothermal amplification reaction for detection and identification of Candida albicans, Candida auris and Candida glabrata using fluorescent probe
abstract The present invention relates to a real-time multiplex LAMP primer set for differential detection of Candida albicans , Candida auris , and Candida glabrata , , since it was produced based on the 18s-28s rRNA gene sequence including the ITS2 region, the electrophoresis process is unnecessary compared to conventional PCR and real time PCR-based detection, and there is no temperature change required for the test, so Candida detection time This short, economical and lightweight device has the advantage of being available. In addition, the present invention maintains the accuracy of diagnosis in that it can detect and simultaneously detect Candida albican, Candida auris, and Candida glabrata in one tube using an additional fluorescent probe and a quencher of a complementary sequence. Since it is advantageous in terms of time and cost, it is expected to be used as a molecular diagnostic test method replacing the existing fungal detection method.
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