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Journal ArticleDOI

Avoiding false positives with PCR

S Kwok, +1 more
- 18 May 1989 - 
- Vol. 339, Iss: 6221, pp 237-238
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TLDR
The exquisite sensitivity of the polymerase chain reaction means DNA contamination can ruin an entire experiment and adherence to a strict set of protocols can avoid disaster.
Abstract
The exquisite sensitivity of the polymerase chain reaction means DNA contamination can ruin an entire experiment. Tidiness and adherence to a strict set of protocols can avoid disaster.

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Citations
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Journal ArticleDOI

CNS microvascular pericytes exhibit multipotential stem cell activity.

TL;DR: It is reported here that adult central nervous system capillaries contain a distinct population of microvascular cells, the pericyte that are nestin/NG2 positive and in response to basic fibroblast growth factor (bFGF) differentiate into cells of neural lineage.
Journal ArticleDOI

A quantitative PCR method for measuring absolute telomere length

TL;DR: This method is based on the Cawthon method for relative measurement of telomere length (TL) but modified by introducing an oligomer standard to measure aTL, making it amenable for molecular epidemiological studies.
Journal ArticleDOI

Two-way cell traffic between mother and fetus : Biologic and clinical implications

TL;DR: The bilateral trafficking of nucleated cells between the fetus and the mother was studied using polymerase chain reaction (PCR)-based systems sensitive enough to detect 1 target cell in 100,000 background cells.
Journal ArticleDOI

Sensitive detection of Helicobacter pylori by using polymerase chain reaction.

TL;DR: The detection of H. pylori by PCR will enable both retrospective and prospective analyses of clinical samples, elucidating the role of this organism in gastroduodenal disease.
Journal ArticleDOI

Decrease in serum hepatitis C viral RNA during alpha-interferon therapy for chronic hepatitis C

TL;DR: In this article, the effect of alpha-interferon therapy on hepatitis C viral RNA in serum of patients with chronic hepatitis C was evaluated. But, the results were limited.
References
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Journal ArticleDOI

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

TL;DR: A thermostable DNA polymerase was used in an in vitro DNA amplification procedure, the polymerase chain reaction, which significantly improves the specificity, yield, sensitivity, and length of products that can be amplified.
Book ChapterDOI

Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

TL;DR: A method whereby a nucleic acid sequence can be exponentially amplified in vitro is described in the chapter, and the possibility of utilizing a heat-stable DNA polymerase is explored so as to avoid the need for addition of new enzyme after each cycle of thermal denaturation.
Journal ArticleDOI

DNA amplification for direct detection of HIV-1 in DNA of peripheral blood mononuclear cells

TL;DR: This method of DNA amplification made it possible to obtain results within 3 days, whereas virus isolation takes up to 3 to 4 weeks, and may therefore be used to complement or replace virus isolation as a routine means of determining HIV-1 infection.
Journal ArticleDOI

DNA typing from single hairs

TL;DR: Three different means of DNA typing are used for the determination of amplified DNA fragment length differences, hybridization with allele-specific oligonucleotide probes, and direct DNA sequencing on single human hairs to detect genetically variable mitochondrial and nuclear DNA sequences.
Journal ArticleDOI

Amplification and analysis of DNA sequences in single human sperm and diploid cells

TL;DR: The use of the polymerase chain reaction for analysing DNA sequences in individual diploid cells and human sperm shows that two genetic loci can be co-amplified from a single sperm, which may allow the analysis of previously inaccessible genetic phenomena.
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