Single Cell Diagnostics

  • Thornhill A
ISSN: 1543-1894
N/ACitations
Citations of this article
40Readers
Mendeley users who have this article in their library.

Abstract

Accurate detection of gene sequences in single cells is the ultimate challenge to polymerase chain reaction (PCR) sensitivity. Unfortunately, commonly used conventional and real-time PCR techniques are often too unreliable at that level to provide the accuracy needed for clinical diagnosis. Here we provide details of linear-after-the-exponential-PCR (LATE-PCR), a method similar to asymmetric PCR in the use of primers at different concentrations, but with novel design criteria to ensure high efficiency and specificity. Compared with conventional PCR, LATE-PCR increases the signal strength and allele discrimination capability of oligonucleotide probes such as molecular beacons and reduces variability among replicate samples. The analysis of real-time kinetics of LATEPCR signals provides a means for improving the accuracy of single cell genetic diagnosis.

Cite

CITATION STYLE

APA

Thornhill, A. (2007). Single Cell Diagnostics. Cell, 132. Retrieved from http://www.springerlink.com/index/10.1007/978-1-59745-298-4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free