Rapid detection of GYPA, LDLR, HBGG, D7S8 and GC alleles by real-time fluorescence PCR

被引:0
|
作者
Nata, M [1 ]
Hashiyada, M [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Div Forens Med, Dept Publ Hlth & Forens Med,Aoba Ku, Sendai, Miyagi 9808575, Japan
来源
关键词
allele-specific TaqMan PCR assay; SYBR green PCR assay; AmpliType PM kit; TaqMan probe; additional mismatch;
D O I
10.1016/S0531-5131(02)00567-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We developed the allele-specific TaqMan polymerase chain reaction (AS-TaqMan PCR) and SYBR Green PCR assays for detecting glycophorin A (GYPA), low-density lipoprotein receptor (LDLR), hemoglobin G (HBGG), D7S8 and group-specific component (GC) alleles. We improved the specificity of detecting a nucleotide substitution by introducing tile additional mismatches at position 2 (3 in GYPA). The differences between threshold cycle (0) values of different genotypes on each of the loci were statistically significantly different. All the genotypes agreed with the results using the AmpliType PM+DQAl PCR Amplification and Typing kit. The AS-TaqMan PCR and SYBR Green PCR assays are simple, rapid, and accurate, as well as suitable for high-throughput applications in a forensic investigation. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
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