| Literature DB >> 24831451 |
Simone L Marasso1, Domenico Mombello, Matteo Cocuzza, Davide Casalena, Ivan Ferrante, Alessandro Nesca, Piret Poiklik, Kadri Rekker, Anu Aaspollu, Sergio Ferrero, Candido F Pirri.
Abstract
In this work a polymer lab-on-a-chip (LOC), fabricated through MEMS technology, was employed to execute a genetic protocol for the Single Nucleotide Polymorphisms (SNPs) detection. The LOC was made in Poly (methyl methacrylate) (PMMA) and has two levels: the lower one for the insertion and mixing of the reagents, the upper one for the interfacing with the DNA microarray chip. The hereditary hearing loss was chosen as case of study, since the demand for testing such a particular disorder is high and genetics behind the condition is quite clear. The Arrayed Primer EXtension (APEX) genetic protocol was implemented on the LOC to analyze the SNPs. A low density (for detection of up to 10 mutations) and a high density microarray chips (for detection of 245 mutations in 12 genes), containing the primers for the extension, were employed to carry out the APEX reaction on the LOC. Both the microarray chips provide a signal to noise ratio and efficiency comparable with a detection obtained in a conventional protocol in standard conditions. Moreover, significant reduction of the employed PCR volume (from 30 μL to 10 μL) was obtained using the low density chip.Entities:
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Year: 2014 PMID: 24831451 DOI: 10.1007/s10544-014-9869-x
Source DB: PubMed Journal: Biomed Microdevices ISSN: 1387-2176 Impact factor: 2.838