Multiplexed on-chip real-time PCR using hydrogel spot array for microRNA profiling of minimal tissue samples

Authors
Jung, SeungwonKim, Bong KyunLee, SangjoonYoon, SeungminIm, Heh-InKim, Sang Kyung
Issue Date
2018-06-01
Publisher
ELSEVIER SCIENCE SA
Citation
SENSORS AND ACTUATORS B-CHEMICAL, v.262, pp.118 - 124
Abstract
Since microRNAs (miRNAs) have been considered as regulators of messenger RNA ( mRNA) translation, the development of the simple, multiplex, and quantitatively precise miRNA profiling techniques becomes more significant. Here, an on-chip multiplex real-time quantitative polymerase chain reaction (qPCR) for miRNA profiling is demonstrated with a primer-immobilized network (PIN) array, which consists of hundreds of hydrogel spots. The array renders highly dense reaction cells of 20 x 20 in 1 cm(2). Uniform performance of the 400 real-time PCR reservoirs was achieved through our fabrication process. The amplicons and their fluorescent signals were isolated in each hydrogel spot, whose detection limit was measured to 16 aM, covering a seven-log concentration range. With the PIN spots of different primers, multiple miRNAs could be quantified in a single reaction out of very limited amount of RNA. For proof of concept, ten different miRNAs from the medial habenula of a mouse which is small region of the brain were successfully analyzed. (C) 2018 Elsevier B.V. All rights reserved.
Keywords
GENE-EXPRESSION MEASUREMENTS; SYSTEM; CDNA; GENE-EXPRESSION MEASUREMENTS; SYSTEM; CDNA; MicroRNA; Real-time PCR; Hydrogel; Polyethylene glycol; Primer-immobilized network; Medial habenula
ISSN
0925-4005
URI
https://pubs.kist.re.kr/handle/201004/121269
DOI
10.1016/j.snb.2018.01.228
Appears in Collections:
KIST Article > 2018
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