Jung, Seungwon Kim, Bong Kyun Lee, Sangjoon Yoon, Seungmin Im, Heh-In Kim, Sang Kyung 2024-01-19T22:32:26Z 2024-01-19T22:32:26Z 2021-09-03 2018-06-01 0925-4005 https://pubs.kist.re.kr/handle/201004/121269 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. English ELSEVIER SCIENCE SA GENE-EXPRESSION MEASUREMENTS SYSTEM CDNA Multiplexed on-chip real-time PCR using hydrogel spot array for microRNA profiling of minimal tissue samples Article 10.1016/j.snb.2018.01.228 1 SENSORS AND ACTUATORS B-CHEMICAL, v.262, pp.118 - 124 SENSORS AND ACTUATORS B-CHEMICAL 262 118 124 scie scopus 000427460600016 2-s2.0-85042945239 Chemistry, Analytical Electrochemistry Instruments & Instrumentation Chemistry Electrochemistry Instruments & Instrumentation Article GENE-EXPRESSION MEASUREMENTS SYSTEM CDNA MicroRNA Real-time PCR Hydrogel Polyethylene glycol Primer-immobilized network Medial habenula