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  4. A molecular fraction collecting tool for the ABI 310 automated sequencer
 
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A molecular fraction collecting tool for the ABI 310 automated sequencer

Journal
Journal of Molecular Diagnostics
Journal Volume
9
Journal Issue
5
Pages
598-603
Date Issued
2007
Author(s)
Lin M.-T.
Rich R.G.
Shipley R.F.
Hafez M.J.
LI-HUI TSENG  
Murphy K.M.
Gocke C.D.
Eshleman J.R.
DOI
10.2353/jmoldx.2007.070022
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-36349015373&doi=10.2353%2fjmoldx.2007.070022&partnerID=40&md5=f486b94257e89b833cb1b3fa898b2b1e
https://scholars.lib.ntu.edu.tw/handle/123456789/597130
Abstract
Several methods exist to retrieve and purify DNA fragments after agarose or polyacrylamide gel electrophoresis for subsequent analyses. However, molecules present in low concentration and molecules similar in size to their neighbors are difficult to purify. Capillary electrophoresis has become popular in molecular diagnostic laboratories because of its automation, excellent resolution, and high sensitivity. In the current study, the ABI Prism 310 Genetic Analyzer was reconfigured into a fraction collector by adapting the standard gel block to accommodate a collection tube at the distal end of capillary. The time to collect the desired peaks was estimated by extrapolating from standard capillary electrophoresis using the original gel block. Fraction collection from a mixture of DNA fragments amplified from wild type and several internal tandem duplication mutations of the FMS-like tyrosine kinase 3 (Flt3) gene yielded highly purified DNA fragments containing internal tandem duplication mutations and predictable electrokinetics using the reconstructed gel block. The reconfigured instrument could successfully isolate DNA amplicons from extremely low-amplitude peaks (110 relative fluorescent units), which were undetectable using polyacrylamide gel electrophoresis. In addition, we successfully isolated bands that were only three bases apart that comigrated on polyacrylamide gel electrophoresis. DNA sequencing was used to confirm that the correct peaks were recovered at sufficient purity.
Publisher
Association of Molecular Pathology
Type
journal article

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