Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Solving the "world-to-chip" interface problem with a microfluidic matrix.

Jian Liu1, Carl Hansen, Stephen R Quake

  • 1Department of Chemistry, California Institute of Technology, Pasadena, California 91125, USA.

Analytical Chemistry
|December 17, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Computed tomography urography with corticomedullary phase can exclude urinary bladder cancer with high accuracy.

BMC urology·2022
Same author

Isolation of monoclonal antibodies from anti-synthetase syndrome patients and affinity maturation by recombination of independent somatic variants.

mAbs·2020
Same author

The miR-185/PAK6 axis predicts therapy response and regulates survival of drug-resistant leukemic stem cells in CML.

Blood·2020
Same author

Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing.

Cell·2019
Same author

A topological view of human CD34<sup>+</sup> cell state trajectories from integrated single-cell output and proteomic data.

Blood·2019
Same author

Single-cell analysis identifies a CD33<sup>+</sup> subset of human cord blood cells with high regenerative potential.

Nature cell biology·2018
Same journal

The ACS at 150: The History of Analytical Chemistry Publications and a Century of Progress.

Analytical chemistry·2026
Same journal

Machine Learning-Enabled Image Analysis of Complex Chemical Mixtures: Synthetic Urine Droplets as a Test System.

Analytical chemistry·2026
Same journal

H<sub>2</sub>O<sub>2</sub>/Viscosity Tandem-Locked Fluorescent Probes Based on an In Situ Fluorophore Synthesis Strategy for Colitis Imaging and Diagnosis.

Analytical chemistry·2026
Same journal

TopoStitcher: A Geometric-Topological Structure-Guided Stitching Framework for Single-Molecule Localization Microscopy.

Analytical chemistry·2026
Same journal

Noninvasive SERS Immunosensing of Tyrosinase for Melanoma Monitoring via Microneedle Sampling Integrated with Satellite-Structured Bifunctional Nanozymes.

Analytical chemistry·2026
Same journal

Label-Free Electrochemical CRISPR Platform Gated by Allosteric Transcription Factors for Ultrasensitive Small-Molecule Detection.

Analytical chemistry·2026
See all related articles

Microfluidic technology significantly reduces pipetting steps for complex assays like polymerase chain reaction (PCR). This innovation minimizes reagent use and sample handling, enabling cost-effective, large-scale biological experiments.

Area of Science:

  • Biotechnology
  • Chemical Engineering
  • Molecular Biology

Background:

  • Traditional fluid handling for molecular assays is complex and reagent-intensive.
  • Scaling up experiments like polymerase chain reaction (PCR) requires numerous manual pipetting steps.
  • The macroscopic/microfluidic interface presents a challenge for automated, high-throughput assays.

Purpose of the Study:

  • To develop a microfluidic solution addressing the macroscopic/microfluidic interface issue.
  • To demonstrate significant economies of scale in pipetting operations using microfluidics.
  • To reduce reagent consumption and sample overhead in high-throughput biological assays.

Main Methods:

  • Implementation of an N x N microfluidic matrix (N=20) with 3-nL reactors at each vertex.

Related Experiment Videos

  • Amortization of a single 2-microL polymerase aliquot across 400 independent reactions.
  • Development of a novel method for automated fluid handling at the microfluidic interface.
  • Main Results:

    • Performed 400 distinct PCR reactions using only 41 pipetting steps.
    • Reduced pipetting steps by over 96% compared to conventional fluid handling (41 vs. 1200 steps).
    • Dramatically minimized sample overhead and reagent consumption through shared reagent aliquots.

    Conclusions:

    • Microfluidic matrix chips offer an effective solution for complex pipetting operations.
    • This technology enables significant economies of scale for assays like PCR.
    • The developed method provides a general platform for automated, low-volume chemical and biological experiments.