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 Concept Videos

Sanger Sequencing01:57

Sanger Sequencing

DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Labeling DNA Probes03:31

Labeling DNA Probes

DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...

You might also read

Related Articles

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

Sort by
Same author

Raman mapping on Ag-covered nanostructured substrates as an innovative approach for rapid estimation of post-mortem interval on human whole blood.

International journal of legal medicine·2026
Same author

The impact of near-infrared photobiomodulation therapy on human oocyte rescue in vitro maturation.

Journal of photochemistry and photobiology. B, Biology·2026
Same author

Lactate-mediated NK cell dysfunction as a prognostic marker and therapeutic target in breast cancer.

Cell death discovery·2026
Same author

Applications of Raman spectroscopy in the post-mortem interval estimation: a systematic literature review.

International journal of legal medicine·2026
Same author

Effect of human papillomavirus infection on semen quality and assisted reproductive technology outcomes: a prospective observational cohort study.

BMC medicine·2025
Same author

Analysis of Single Nuclei in a Microfluidic Cytometer Towards Metaphase Enrichment.

Electrophoresis·2025

Related Experiment Video

Updated: May 29, 2026

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

"DNA-Dressed NAnopore" for complementary sequence detection.

Valentina Mussi1, Paola Fanzio, Luca Repetto

  • 1Nanomed Labs, Physics Department, University of Genova, and Nanobiotechnologies, National Institute for Cancer Research (IST), Largo R. Benzi, 10, Genova 16132, Italy. mussi@fisica.unige.it

Biosensors & Bioelectronics
|August 27, 2011
PubMed
Summary
This summary is machine-generated.

This study introduces DNA-Dressed Nanopores (DNA2) for single-molecule sensing. These novel biosensors can selectively detect complementary DNA sequences, advancing molecular diagnostics.

More Related Videos

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
07:16

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

Published on: February 9, 2024

Nanopore DNA Sequencing for Metagenomic Soil Analysis
07:33

Nanopore DNA Sequencing for Metagenomic Soil Analysis

Published on: December 14, 2017

Related Experiment Videos

Last Updated: May 29, 2026

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
07:16

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

Published on: February 9, 2024

Nanopore DNA Sequencing for Metagenomic Soil Analysis
07:33

Nanopore DNA Sequencing for Metagenomic Soil Analysis

Published on: December 14, 2017

Area of Science:

  • Nanotechnology
  • Molecular Biology
  • Biophysics

Background:

  • Single molecule electrical sensing using nanopores is a rapidly advancing field with significant potential in bioanalytics and diagnostics.
  • Nanopore sensing relies on detecting conductance changes as molecules pass through a nanometer-sized channel.
  • Surface functionalization of nanopores allows for tailored molecular recognition and binding capabilities.

Purpose of the Study:

  • To develop and demonstrate a novel class of selective biosensor devices, termed DNA-Dressed Nanopores (DNA2).
  • To investigate the capability of DNA2 devices for single-molecule DNA translocation and hybridization experiments.
  • To assess the selective detection of complementary DNA sequences using functionalized nanopores.

Main Methods:

  • Fabrication of solid-state nanopores with initially large dimensions.
  • Resizing and activation of nanopores through functionalization with DNA molecules to create DNA2 devices.
  • Conducting single-molecule electrical sensing experiments to monitor DNA translocation and hybridization events.

Main Results:

  • Demonstrated successful DNA translocation and hybridization at the single-molecule level using DNA2 devices.
  • Showcased the selective detection of complementary DNA target sequences based on molecular affinity.
  • Confirmed the ability of DNA2 to differentiate between molecules based on their binding interactions with the functionalized surface.

Conclusions:

  • DNA-Dressed Nanopores (DNA2) represent a novel and effective platform for selective single-molecule DNA detection.
  • The DNA2 technology holds promise for the development of integrable, parallel devices for mutation analysis and diagnostics.
  • This approach advances the field of nanopore-based bioanalytical investigations and molecular diagnostics.