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Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1933-8. doi: 10.1073/pnas.0305476101. Epub 2004 Feb 9.
2
Two-temperature LATE-PCR endpoint genotyping.双温度晚期聚合酶链反应终点基因分型
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Linear-After-The-Exponential (LATE)-PCR: primer design criteria for high yields of specific single-stranded DNA and improved real-time detection.指数后线性(LATE)-PCR:用于高产量特异性单链DNA及改进实时检测的引物设计标准
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Monoplex/multiplex linear-after-the-exponential-PCR assays combined with PrimeSafe and Dilute-'N'-Go sequencing.单重/多重指数后线性PCR检测与PrimeSafe和稀释即测序相结合。
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[Polymerase chain reaction, cold probes and clinical diagnosis].[聚合酶链反应、冷探针与临床诊断]
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本文引用的文献

1
Genotyping SNPs with molecular beacons.使用分子信标对单核苷酸多态性进行基因分型。
Methods Mol Biol. 2003;212:111-28. doi: 10.1385/1-59259-327-5:111.
2
Real-time PCR with molecular beacons provides a highly accurate assay for detection of Tay-Sachs alleles in single cells.使用分子信标的实时聚合酶链反应为单细胞中泰-萨克斯等位基因的检测提供了一种高度准确的测定方法。
Prenat Diagn. 2002 Dec;22(12):1130-4. doi: 10.1002/pd.500.
3
QuantiLyse: reliable DNA amplification from single cells.定量裂解:从单细胞进行可靠的DNA扩增。
Biotechniques. 2002 May;32(5):1106-11. doi: 10.2144/02325pf01.
4
Minor groove binder-conjugated DNA probes for quantitative DNA detection by hybridization-triggered fluorescence.用于通过杂交触发荧光进行定量DNA检测的小沟结合剂共轭DNA探针。
Biotechniques. 2002 Apr;32(4):940-4, 946-9. doi: 10.2144/02324pf01.
5
Real-time PCR in virology.病毒学中的实时聚合酶链反应
Nucleic Acids Res. 2002 Mar 15;30(6):1292-305. doi: 10.1093/nar/30.6.1292.
6
MELTING, computing the melting temperature of nucleic acid duplex.熔解,计算核酸双链体的熔解温度
Bioinformatics. 2001 Dec;17(12):1226-7. doi: 10.1093/bioinformatics/17.12.1226.
7
Molecular epidemiology of Tay-Sachs disease.泰-萨克斯病的分子流行病学
Adv Genet. 2001;44:233-52. doi: 10.1016/s0065-2660(01)44083-1.
8
Naturally occurring mutations in GM2 gangliosidosis: a compendium.GM2神经节苷脂贮积症的自然发生突变:简编
Adv Genet. 2001;44:199-224. doi: 10.1016/s0065-2660(01)44081-8.
9
Real-time PCR using molecular beacons for accurate detection of the Y chromosome in single human blastomeres.使用分子信标进行实时聚合酶链反应以准确检测单个人类卵裂球中的Y染色体。
Mol Hum Reprod. 2000 Dec;6(12):1155-64. doi: 10.1093/molehr/6.12.1155.
10
Current applications of single-cell PCR.单细胞PCR的当前应用。
Cell Mol Life Sci. 2000 Jan 20;57(1):96-105. doi: 10.1007/s000180050501.

指数后线性(LATE)-PCR:一种先进的不对称PCR方法及其在定量实时分析中的应用

Linear-after-the-exponential (LATE)-PCR: an advanced method of asymmetric PCR and its uses in quantitative real-time analysis.

作者信息

Sanchez J Aquiles, Pierce Kenneth E, Rice John E, Wangh Lawrence J

机构信息

Department of Biology, MS 008, Brandeis University, 415 South Street, Waltham, MA 02454-9110, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1933-8. doi: 10.1073/pnas.0305476101. Epub 2004 Feb 9.

DOI:10.1073/pnas.0305476101
PMID:14769930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC357030/
Abstract

Conventional asymmetric PCR is inefficient and difficult to optimize because limiting the concentration of one primer lowers its melting temperature below the reaction annealing temperature. Linear-After-The-Exponential (LATE)-PCR describes a new paradigm for primer design that renders assays as efficient as symmetric PCR assays, regardless of primer ratio. LATE-PCR generates single-stranded products with predictable kinetics for many cycles beyond the exponential phase. LATE-PCR also introduces new probe design criteria that uncouple hybridization probe detection from primer annealing and extension, increase probe reliability, improve allele discrimination, and increase signal strength by 80-250% relative to symmetric PCR. These improvements in PCR are particularly useful for real-time quantitative analysis of target numbers in small samples. LATE-PCR is adaptable to high throughput applications in fields such as clinical diagnostics, biodefense, forensics, and DNA sequencing. We showcase LATE-PCR via amplification of the cystic fibrosis CFDelta508 allele and the Tay-Sachs disease TSD 1278 allele from single heterozygous cells.

摘要

传统的不对称PCR效率低下且难以优化,因为限制一种引物的浓度会使其解链温度降至反应退火温度以下。指数后线性(LATE)-PCR描述了一种新的引物设计范式,无论引物比例如何,该方法都能使检测效率与对称PCR检测一样高。LATE-PCR在指数期后的多个循环中产生具有可预测动力学的单链产物。LATE-PCR还引入了新的探针设计标准,使杂交探针检测与引物退火和延伸解耦,提高了探针的可靠性,改善了等位基因区分,并使信号强度相对于对称PCR提高了80%-250%。PCR的这些改进对于小样本中靶标数量的实时定量分析特别有用。LATE-PCR适用于临床诊断、生物防御、法医学和DNA测序等领域的高通量应用。我们通过从单个杂合细胞中扩增囊性纤维化CFDelta508等位基因和泰-萨克斯病TSD 1278等位基因来展示LATE-PCR。