| Literature DB >> 11233602 |
Y F Leung1, P O Tam, W C Tong, L Baum, K W Choy, D S Lam, C P Pang.
Abstract
High-throughput screening for single nucleotide polymorphisms (SNPs) or mutations can be achieved by inexpensive technologies. We modified the original protocols of conformation-sensitive gel electrophoresis (CSGE) to increase throughput several fold to 1.3 samples/min, which is about five times faster than denaturing high-performance liquid chromatography (DHPLC). The modifications include decreasing the gel thickness, increasing the number of lanes to 96, and increasing the number of samples per lane to seven. This high-throughput CSGE method is fast, robust, and as simple as the original protocols. Together with a two-stage strategy for screening homozygotes and the replacement of ethidium bromide with SYBR Gold DNA dye staining, this protocol is a reliable and cost-effective alternative for laboratories that require high-throughput screening.Entities:
Mesh:
Year: 2001 PMID: 11233602 DOI: 10.2144/01302tt02
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993