Quantification of cDNA on GMR biosensor array towards point-of-care gene expression analysis.

Biosens Bioelectron

Department of Materials Science and Engineering, Stanford University, Stanford, CA 93405, USA; Department of Electrical Engineering, Stanford University, Stanford, CA 93405, USA. Electronic address:

Published: April 2019

Gene expression analysis at the point-of-care is important for rapid disease diagnosis, but traditional techniques are limited by multiplexing capabilities, bulky equipment, and cost. We present a gene expression analysis platform using a giant magnetoresistive (GMR) biosensor array, which allows multiplexed transcript detection and quantification through cost-effective magnetic detection. In this work, we have characterized the sensitivity, dynamic range, and quantification accuracy of Polymerase chain reaction (PCR)-amplified complementary DNA (cDNA) on the GMR for the reference gene GAPDH. A synthetic GAPDH single-stranded DNA (ssDNA) standard was used to calibrate the detection, and ssDNA dilutions were qPCR-amplified to obtain a standard curve. We demonstrate that the GMR platform provides a dynamic range of 4 orders of magnitude and a limit of detection of 1 pM and 0.1 pM respectively for 15 and 18-cycle amplified synthetic GAPDH PCR products. The quantitative results of GMR analysis of cell-line RNA were confirmed by qPCR.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391206PMC
http://dx.doi.org/10.1016/j.bios.2018.09.050DOI Listing

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