Literature DB >> 10862086

Higher resolution microplate array diagonal gel electrophoresis: application to a multiallelic minisatellite.

S D O'Dell1, X Chen, I N Day.   

Abstract

The 5' polymorphic region of the insulin (INS, MIM# 176730) gene contains a variable tandem repetition of 14-15 bp (a variable number of tandem repeats (VNTR) locus). After PCR amplification, we achieved precise sizing of class I alleles (range 641 to 843 bp) on 96-well open-face polyacrylamide microplate array diagonal gel electrophoresis (MADGE) gels, obtaining resolution of the 2% mobility difference which represents one tandem repeat. PCR products were run double-stranded, but no additional bands were generated except in the case of differences of three, two, and one repeat between alleles; none compromised allele identification, and in the latter case the heteroduplex was a useful confirmation signal. No end labelling of primers was required, as the sensitive Vistra Green intercalating dye for double strands was used for visualization of bands from diluted samples. Duracryl, a high mechanical-strength polyacrylamide derivative, proved to have good resolution properties for electrophoresis. A co-run ladder ensured precise binning without inter-lane variability. Simultaneous electrophoresis of gels in a thermostatically controlled tank allowed up to 1,000 samples to be run in 90 min. Gels were analyzed using a FluorImager 595 fluorescent scanning system, and alleles identified using a combination of Phoretix software for band migration measurement and Microsoft Excel to compute allele sizes. Unlike other systems for minisatellite allele sizing, throughput was not limited (in time or cost) by electrophoresis. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10862086     DOI: 10.1002/1098-1004(200006)15:6<565::AID-HUMU8>3.0.CO;2-7

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  4 in total

1.  Manual 768 or 384 well microplate gel 'dry' electrophoresis for PCR checking and SNP genotyping.

Authors:  Tom R Gaunt; Lesley J Hinks; Hamid Rassoulian; Ian N M Day
Journal:  Nucleic Acids Res       Date:  2003-05-01       Impact factor: 16.971

2.  In vitro repair of complex unligatable oxidatively induced DNA double-strand breaks by human cell extracts.

Authors:  E Pastwa; R D Neumann; T A Winters
Journal:  Nucleic Acids Res       Date:  2001-08-15       Impact factor: 16.971

3.  MeltMADGE for mutation scanning of specific genes in population studies.

Authors:  Khalid K Alharbi; Mohammed A Aldahmesh; Tom R Gaunt; Hamid Rassoulian; Philip Ai Guthrie; Santiago Rodriguez; Christopher R Boustred; Emmanuel Spanakis; Ian N M Day
Journal:  Nat Protoc       Date:  2010-10-21       Impact factor: 13.491

4.  Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population.

Authors:  Khalid K Alharbi; Mohammed A Aldahmesh; Emmanuel Spanakis; Lema Haddad; Roslyn A Whittall; Xiao-he Chen; Hamid Rassoulian; Matt J Smith; Julie Sillibourne; Nicola J Ball; Nikki J Graham; Patricia J Briggs; Iain A Simpson; David I W Phillips; Deborah A Lawlor; Shu Ye; Stephen E Humphries; Cyrus Cooper; George Davey Smith; Shah Ebrahim; Diana M Eccles; Ian N M Day
Journal:  Genome Res       Date:  2005-07       Impact factor: 9.043

  4 in total

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