Literature DB >> 7818902

Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods.

A Vidal-Puig1, D E Moller.   

Abstract

Single-strand conformation polymorphism (SSCP) analysis is a genetic screening technique that allows for the rapid detection of single nucleotide substitutions in fragments of PCR-amplified genomic DNA or cDNA. Several alternative protocols are now being commonly used to resolve differences in electrophoretic mobility of single-stranded DNA fragments. The aim of this study was to directly compare the sensitivity of three popular SSCP methods using a panel of 19 known human mutations/polymorphisms present in genomic DNA samples. Using a single electrophoresis protocol, 95% of the mutations were detected using small-format PhastGel and the PhastSystem. Large-format gels (5% polyacrylamide and Hydrolink-MDE) were tested both with and without the addition of 10% glycerol. The sensitivity for polyacrylamide and Hydrolink-MDE gels without glycerol was 89% and 79%, respectively, and 68% or 63%, respectively, for glycerol-containing gels. However, all mutations were detected with either polyacrylamide or Hydrolink-MDE when both glycerol and non-glycerol gels were examined. We conclude that comparable very high detection efficiency can be achieved using the PhastSystem or by using a combination of two large-gel conditions with either polyacrylamide or Hydrolink-MDE.

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Year:  1994        PMID: 7818902

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  20 in total

1.  Mutation screening of the muscarinic M(2) and M(3) receptor genes in normal and asthmatic subjects.

Authors:  A G Fenech; M J Ebejer; A E Felice; R Ellul-Micallef; I P Hall
Journal:  Br J Pharmacol       Date:  2001-05       Impact factor: 8.739

2.  Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.

Authors:  P Kozlowski; W J Krzyzosiak
Journal:  Nucleic Acids Res       Date:  2001-07-15       Impact factor: 16.971

3.  Signals sustaining human immunoglobulin V gene hypermutation in isolated germinal centre B cells.

Authors:  K Dahlenborg; J D Pound; J Gordon; C A Borrebaeck; R Carlsson
Journal:  Immunology       Date:  2000-10       Impact factor: 7.397

4.  A new allele of the lurcher gene, lurcherJ.

Authors:  P L De Jager; J Zuo; S A Cook; N Heintz
Journal:  Mamm Genome       Date:  1997-09       Impact factor: 2.957

5.  An approximately 1.2-Mb bacterial artificial chromosome contig refines the genetic and physical maps of the lurcher locus on mouse chromosome 6.

Authors:  P L De Jager; J Zuo; N Heintz
Journal:  Genome Res       Date:  1997-07       Impact factor: 9.043

6.  In vivo accumulation of the same anti-melanoma T cell clone in two different metastatic sites.

Authors:  M Hishii; D Andrews; L A Boyle; J T Wong; F Pandolfi; P J van den Elsen; J T Kurnick
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-18       Impact factor: 11.205

7.  Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer.

Authors:  I P Tomlinson; N E Beck; T Homfray; C J Harocopos; W F Bodmer
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

8.  Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas.

Authors:  N E Beck; I P Tomlinson; T F Homfray; I M Frayling; S V Hodgson; W F Bodmer
Journal:  Gut       Date:  1997-08       Impact factor: 23.059

9.  Genetic pathways of colorectal carcinogenesis rarely involve the PTEN and LKB1 genes outside the inherited hamartoma syndromes.

Authors:  Z J Wang; F Taylor; M Churchman; G Norbury; I Tomlinson
Journal:  Am J Pathol       Date:  1998-08       Impact factor: 4.307

10.  Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.

Authors:  Peter Hackman; Anna Vihola; Henna Haravuori; Sylvie Marchand; Jaakko Sarparanta; Jerome De Seze; Siegfried Labeit; Christian Witt; Leena Peltonen; Isabelle Richard; Bjarne Udd
Journal:  Am J Hum Genet       Date:  2002-07-26       Impact factor: 11.025

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