Unknown

Dataset Information

0

Nuclemeter: a reaction-diffusion based method for quantifying nucleic acids undergoing enzymatic amplification.


ABSTRACT: Real-time amplification and quantification of specific nucleic acid sequences plays a major role in medical and biotechnological applications. In the case of infectious diseases, such as HIV, quantification of the pathogen-load in patient specimens is critical to assess disease progression and effectiveness of drug therapy. Typically, nucleic acid quantification requires expensive instruments, such as real-time PCR machines, which are not appropriate for on-site use and for low-resource settings. This paper describes a simple, low-cost, reaction-diffusion based method for end-point quantification of target nucleic acids undergoing enzymatic amplification. The number of target molecules is inferred from the position of the reaction-diffusion front, analogous to reading temperature in a mercury thermometer. The method was tested for HIV viral load monitoring and performed on par with conventional benchtop methods. The proposed method is suitable for nucleic acid quantification at point of care, compatible with multiplexing and high-throughput processing, and can function instrument-free.

SUBMITTER: Liu C 

PROVIDER: S-EPMC4256561 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Nuclemeter: a reaction-diffusion based method for quantifying nucleic acids undergoing enzymatic amplification.

Liu Changchun C   Sadik Mohamed M MM   Mauk Michael G MG   Edelstein Paul H PH   Bushman Frederic D FD   Gross Robert R   Bau Haim H HH  

Scientific reports 20141205


Real-time amplification and quantification of specific nucleic acid sequences plays a major role in medical and biotechnological applications. In the case of infectious diseases, such as HIV, quantification of the pathogen-load in patient specimens is critical to assess disease progression and effectiveness of drug therapy. Typically, nucleic acid quantification requires expensive instruments, such as real-time PCR machines, which are not appropriate for on-site use and for low-resource settings  ...[more]

Similar Datasets

| S-EPMC6310013 | biostudies-literature
| S-EPMC5550438 | biostudies-literature
| S-EPMC4518254 | biostudies-other
2020-12-24 | E-MTAB-8508 | biostudies-arrayexpress
| S-EPMC4278771 | biostudies-literature
| S-EPMC8713971 | biostudies-literature
| S-EPMC8179025 | biostudies-literature
| S-EPMC2647313 | biostudies-literature
| S-EPMC4830604 | biostudies-literature
| S-EPMC4736440 | biostudies-literature