Genotyping of a short tandem repeat system using ion-pair reverse-phase high performance liquid chromatography

Citation
Jm. Devaney et al., Genotyping of a short tandem repeat system using ion-pair reverse-phase high performance liquid chromatography, J LIQ CHR R, 24(13), 2001, pp. 1997-2005
Citations number
8
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
ISSN journal
10826076 → ACNP
Volume
24
Issue
13
Year of publication
2001
Pages
1997 - 2005
Database
ISI
SICI code
1082-6076(2001)24:13<1997:GOASTR>2.0.ZU;2-A
Abstract
Ion pair-reverse phase high performance liquid chromatography (IPRP HPLC) i s a method that can be used for the genotyping of short tandem repeats (STR s) in human nuclear DNA. The genotyping of STRs is useful in human identifi cation and parentage testing, gene mapping studies, cancer diagnostics, and diagnosis of hereditary diseases. IPRP HPLC offers an attractive method fo r STR analysis because of the short analysis time, and there is no need for the waste disposal associated with radioisotopic, enzyme-linked, or fluore scence detection systems. We evaluated the use of IPRP HPLC for the sizing and typing of STR alleles from the HUMTHO1 locus on chromosome 11p15.5. The IPRP HPLC conditions (column temperature, flow rate, and percent organi c modifier per minute) were optimized for the separation of PCR products in the size range of 50-434 base pairs. Using the optimized separation condit ions, the alleles of the HUMTHO1 system were sized in their native state (d ouble stranded) with the use of internal markers. The analysis time for the HUMTHO1 locus was less than 14 minutes, and the alleles could be peak capt ured for further examination such as sequencing.