Title
The Implications of Fragmented Genomic DNA Size Range on the Hybridization Efficiency in NanoGene Assay.
Abstract
DNA hybridization-based assays are well known for their ability to detect and quantify specific bacteria. Assays that employ DNA hybridization include a NanoGene assay, fluorescence in situ hybridization, and microarrays. Involved in DNA hybridization, fragmentation of genomic DNA (gDNA) is necessary to increase the accessibility of the probe DNA to the target gDNA. However, there has been no thorough and systematic characterization of different fragmented gDNA sizes and their effects on hybridization efficiency. An optimum fragmented size range of gDNA for the NanoGene assay is hypothesized in this study. Bacterial gDNA is fragmented via sonication into different size ranges prior to the NanoGene assay. The optimum size range of gDNA is determined via the comparison of respective hybridization efficiencies (in the form of quantification capabilities). Different incubation durations are also investigated. Finally, the quantification capability of the fragmented (at optimum size range) and unfragmented gDNA is compared.
Year
DOI
Venue
2018
10.3390/s18082646
SENSORS
Keywords
Field
DocType
DNA fragmentation,optimum size,quantification capability,hybridization efficiency,magnetic beads,quantum dots
Analytical chemistry,DNA fragmentation,Engineering,Computational biology,Quantum dot,genomic DNA
Journal
Volume
Issue
Citations 
18
8.0
0
PageRank 
References 
Authors
0.34
1
3
Name
Order
Citations
PageRank
Xiaofang Wang1367.83
Beelee Chua200.34
Ahjeong Son300.34