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Fully automated platelet isolation on a centrifugal microfluidic device for molecular diagnostics

DC Field Value Language
dc.contributor.authorChi-Ju Kim-
dc.contributor.authorDong Yeob Ki-
dc.contributor.authorJuhee Park-
dc.contributor.authorVijaya Sunkara-
dc.contributor.authorTae-Hyeong Kim-
dc.contributor.authorYooHong Min-
dc.contributor.authorYoon-Kyoung Cho-
dc.date.accessioned2021-01-07T02:50:05Z-
dc.date.accessioned2021-01-07T02:50:05Z-
dc.date.available2021-01-07T02:50:05Z-
dc.date.available2021-01-07T02:50:05Z-
dc.date.created2020-04-20-
dc.date.issued2020-03-
dc.identifier.issn1473-0197-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/9005-
dc.description.abstractPlatelets play crucial roles in hemostasis and immunity. Over the last decades, clinical evidence has revealed the significance of platelets as complementary biomarkers for the detection and treatment of various diseases, including cancer. Due to a lack of well standardized convenient isolation methods for platelets, pre-analytical factors such as complex handling procedures negatively impact the quality of the platelet samples, including overactivation, low purity, and poor reproducibility. This may lead to biased interpretation of various downstream analyses, such as proteomic and genomic analyses. Herein, we describe a fully automated lab-on-a-disc-based method of platelet isolation from a small volume of blood (<1 mL). This method provides higher yields (>4 folds) and purity (>99%) and lower platelet activation than the conventional method. Moreover, it was also superior in the detection of platelet-related RNAs CD41, PF4, and P2Y12 due to lower contamination with white blood cells-
dc.description.uri1-
dc.language영어-
dc.publisherRoyal Society of Chemistry-
dc.titleFully automated platelet isolation on a centrifugal microfluidic device for molecular diagnostics-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000519210000004-
dc.identifier.scopusid2-s2.0-85081135283-
dc.identifier.rimsid71642-
dc.contributor.affiliatedAuthorChi-Ju Kim-
dc.contributor.affiliatedAuthorDong Yeob Ki-
dc.contributor.affiliatedAuthorJuhee Park-
dc.contributor.affiliatedAuthorVijaya Sunkara-
dc.contributor.affiliatedAuthorTae-Hyeong Kim-
dc.contributor.affiliatedAuthorYooHong Min-
dc.contributor.affiliatedAuthorYoon-Kyoung Cho-
dc.identifier.doi10.1039/c9lc01140d-
dc.identifier.bibliographicCitationLab on a Chip, v.20, no.5, pp.949 - 957-
dc.citation.titleLab on a Chip-
dc.citation.volume20-
dc.citation.number5-
dc.citation.startPage949-
dc.citation.endPage957-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthorTUMOR-EDUCATED PLATELETS-
dc.subject.keywordAuthorCELL LUNG-CANCER-
dc.subject.keywordAuthorWHOLE-BLOOD-
dc.subject.keywordAuthorEXTRACELLULAR VESICLES-
dc.subject.keywordAuthorACTIVATED PLATELETS-
dc.subject.keywordAuthorSEPARATION-
dc.subject.keywordAuthorRNA-
Appears in Collections:
Center for Soft and Living Matter(첨단연성물질 연구단) > 1. Journal Papers (저널논문)
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