MagSNiPer: A new single nucleotide polymorphism typing method based on single base extension, magnetic separation, and chemiluminescence

被引:11
|
作者
Kakihara, F
Kurebayashi, Y
Tojo, Y
Tajima, H
Hasegawa, S
Yohda, M
机构
[1] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, Koganei, Tokyo 1848588, Japan
[2] Sekino Clin Pharmacol Clin, Toshima Ku, Tokyo 1710014, Japan
[3] Precis Syst Sci Co Ltd, Matsudo, Chiba 2700025, Japan
关键词
single nucleotide polymorphism; magnetic separation; chemiluminescence; single base extension; cytochrome P450;
D O I
10.1016/j.ab.2005.03.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a new method for typing single nucleotide polymorphisms (SNPs), MagSNiPer, based on single base extension, magnetic separation, and chemiluminescence. Single base nucleotide extension reaction is performed with a biotinylated primer whose 3' terminus is contiguous to the SNP site with a tag-labeled ddNTP. Then the primers are captured by magnetic-coated beads with streptavidin, and unincorporated labeled ddNTP is removed by magnetic separation. The magnetic beads are incubated with anti-tag antibody conjugated with alkaline phosphatase. After the removal of excess conjugates by magnetic separation, SNP typing is performed by measuring chemiluminescence. The incorporation of labeled ddNTP is monitored by chemiluminescence induced by alkaline phosphatase. MagSNiPer is a simple and robust SNP typing method with a wide dynamic range and high sensitivity. Using MagSNiPer, we could perform SNP typing with as little as 10(-17) Mol of template DNA. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:77 / 82
页数:6
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