One-step pipetting and assembly of encoded chemical-laden microparticles for high-throughput multiplexed bioassays
DC Field | Value | Language |
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dc.contributor.author | Su Eun Chung | - |
dc.contributor.author | Jiyun Kim | - |
dc.contributor.author | Dong Yoon Oh | - |
dc.contributor.author | Younghoon Song | - |
dc.contributor.author | Lee S.H. | - |
dc.contributor.author | Min S. | - |
dc.contributor.author | Sunghoon Kwon | - |
dc.date.available | 2015-04-20T06:09:10Z | - |
dc.date.created | 2014-09-12 | ko |
dc.date.issued | 2014-03 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/1094 | - |
dc.description.abstract | One quantitative liquid handling method in conventional assay processes is pipetting, which delivers a precise volume of one sample at a time. As this process becomes laborious and time-consuming as the number of samples increases, researchers in individual laboratories need a way to conduct large-scale assays in a reasonable amount of time and at an affordable cost. Here we report a novel handling technique of chemical substances termed 'partipetting', which allows the one-step pipetting of various chemical-laden hydrogels. We pipette and assemble various types of encoded chemical-laden microparticles in microwell arrays in parallel. The combination of this heterogeneous particle chip and a cell chip induces the release of the chemicals from the hydrogels and, eventually, the chemicals treat the targets. Based on bioassay applications using partipetting, we show its capability in large-scale bioassays, without the need for high-throughput bioassay resources, owing to a reduction in the assay costs and time. © 2014 Macmillan Publishers Limited. All rights reserved. | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | NATURE PUBLISHING GROUP | - |
dc.subject | antineoplastic agent | - |
dc.subject | auranofin | - |
dc.subject | camptothecin | - |
dc.subject | chemical compound | - |
dc.subject | paclitaxel | - |
dc.subject | pkf 118 310 | - |
dc.subject | salicylate sodium | - |
dc.subject | unclassified drug | - |
dc.subject | bioassay | - |
dc.subject | chemical substance | - |
dc.subject | gel | - |
dc.subject | particle size | - |
dc.subject | quantitative analysis | - |
dc.subject | research work | - |
dc.subject | technological development | - |
dc.subject | analytic method | - |
dc.subject | apoptosis | - |
dc.subject | article | - |
dc.subject | bioassay | - |
dc.subject | cell assay | - |
dc.subject | controlled study | - |
dc.subject | cytotoxicity assay | - |
dc.subject | drug cytotoxicity | - |
dc.subject | encoded chemical laden microparticle | - |
dc.subject | high throughput screening | - |
dc.subject | human | - |
dc.subject | human cell | - |
dc.subject | hydrogel | - |
dc.subject | membrane microparticle | - |
dc.subject | osteosarcoma cell | - |
dc.subject | partipetting | - |
dc.subject | reduction | - |
dc.title | One-step pipetting and assembly of encoded chemical-laden microparticles for high-throughput multiplexed bioassays | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000334300400051 | - |
dc.identifier.scopusid | 2-s2.0-84896532822 | - |
dc.identifier.rimsid | 53699 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Su Eun Chung | - |
dc.contributor.affiliatedAuthor | Jiyun Kim | - |
dc.contributor.affiliatedAuthor | Dong Yoon Oh | - |
dc.contributor.affiliatedAuthor | Younghoon Song | - |
dc.contributor.affiliatedAuthor | Sunghoon Kwon | - |
dc.identifier.doi | 10.1038/ncomms4468 | - |
dc.identifier.bibliographicCitation | NATURE COMMUNICATIONS, v.5, pp.3468 | - |
dc.citation.title | NATURE COMMUNICATIONS | - |
dc.citation.volume | 5 | - |
dc.citation.startPage | 3468 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 20 | - |
dc.description.scptc | 23 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |