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Related Concept Videos

Automated Microbial Diagnostics01:24

Automated Microbial Diagnostics

Automated diagnostic analyzers have transformed clinical microbiology by providing rapid and reliable methods for pathogen identification and antibiotic susceptibility testing. Among these systems, the Vitek 2 is widely used because it automates the traditionally labor-intensive processes of microbial identification (ID) and antibiotic susceptibility testing (AST), delivering standardized and timely results that are essential for effective patient care.Microbial Identification with ID CardsThe...

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Related Experiment Video

Updated: Jun 17, 2026

Visual Detection of Multiple Nucleic Acids in a Capillary Array
08:56

Visual Detection of Multiple Nucleic Acids in a Capillary Array

Published on: November 15, 2017

A rapid multiplex assay for nucleic acid-based diagnostics.

Alina Deshpande1, Jason Gans, Steven W Graves

  • 1Decision Applications Division, Mail Stop K551, Los Alamos National Laboratory, Los Alamos, NM 87545, United States. deshpande_a@lanl.gov

Journal of Microbiological Methods
|December 17, 2009
PubMed
Summary
This summary is machine-generated.

We created a fast, single-tube multiplex oligonucleotide ligation-PCR (MOL-PCR) assay for detecting multiple nucleic acid targets simultaneously. This assay shows potential for rapid diagnostics and surveillance of biothreat agents.

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Last Updated: Jun 17, 2026

Visual Detection of Multiple Nucleic Acids in a Capillary Array
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Area of Science:

  • Molecular Biology
  • Biotechnology
  • Diagnostic Assays

Background:

  • Multiplex nucleic acid detection is crucial for diagnostics and surveillance.
  • Existing ligation-based assays can be complex and time-consuming.
  • There is a need for rapid, robust, and simplified multiplex assays.

Purpose of the Study:

  • To develop a rapid, single-tube, multiplex nucleic acid assay.
  • To adapt the assay to a microsphere array detection platform.
  • To demonstrate the assay's utility for detecting biothreat agents.

Main Methods:

  • Developed multiplex oligonucleotide ligation-PCR (MOL-PCR) assay.
  • Utilized a single-tube reaction followed by Luminex microsphere array detection.
  • Designed modular detection probes for target detection, amplification, and capture.

Main Results:

  • Achieved rapid detection (under 4 hours) of diverse nucleic acid signatures.
  • Successfully demonstrated simultaneous detection of unique sequences and single nucleotide polymorphisms.
  • Applied the assay to detect three biothreat agents: B. anthracis, Y. pestis, and F. tularensis.

Conclusions:

  • The multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is rapid, robust, and simplifies multiplex nucleic acid detection.
  • The assay's modular design and microsphere platform enable versatile applications.
  • This assay holds significant potential for use in diagnostics and surveillance, particularly for biothreat agents.