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

DNA-only Transposons02:57

DNA-only Transposons

17.0K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
17.0K

You might also read

Related Articles

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

Sort by
Same author

Machine learning-guided discovery of poly(ethylene terephthalate)-binding modules to enhance durable whole-cell degradation.

Bioresource technology·2026
Same author

Effects of Smoothened Agonist Exposure on Murine Craniofacial Development.

International dental journal·2026
Same author

MMP1 Modulates Head and Neck Squamous Cell Carcinoma Progression and Therapeutic Response Via Tumour Microenvironment.

International dental journal·2026
Same author

Effect of Intracapsular Pressure on Pulp Sensitivity in Teeth Affected by Jaw Cysts: A Clinical Study Combined With Finite Element Analysis.

International dental journal·2026
Same author

Model surgery-guided interpositional arthroplasty with condylar prosthesis replacement for temporomandibular joint ankylosis: a preliminary single-center case series study.

BMC oral health·2026
Same author

Boron-doped diamond solution-gate field-effect transistor (BDD-SGFET) biosensor for gene mutation detection.

Microsystems & nanoengineering·2026
Same journal

Self-Powered Fine Dust Filtration Using Triboelectrification-Induced Electric Field.

Nanoscale research letters·2022
Same journal

Bio-distribution of Carbon Nanoparticles Studied by Photoacoustic Measurements.

Nanoscale research letters·2022
Same journal

Effects of High-Temperature Growth of Dislocation Filter Layers in GaAs-on-Si.

Nanoscale research letters·2022
Same journal

Correction: Assembly of Carbon Dots into Frameworks with Enhanced Stability and Antibacterial Activity.

Nanoscale research letters·2022
Same journal

Improved Subthreshold Characteristics by Back-Gate Coupling on Ferroelectric ETSOI FETs.

Nanoscale research letters·2022
Same journal

Gold Nanoparticles Enhancing Generation of ROS for Cs-137 Radiotherapy.

Nanoscale research letters·2022
See all related articles

Related Experiment Video

Updated: Dec 24, 2025

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
09:43

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores

Published on: October 31, 2013

14.0K

Controlling DNA Translocation Through Solid-state Nanopores.

Zhishan Yuan1, Youming Liu2, Min Dai2

  • 1School of Electro-mechanical Engineering, Guangdong University of Technology, Guangzhou, 510006, China. yzshan044@163.com.

Nanoscale Research Letters
|April 17, 2020
PubMed
Summary
This summary is machine-generated.

Solid-state nanopores show promise for DNA sequencing but face challenges in spatial and temporal resolution. Controlling DNA translocation speed is key to improving nanopore detection and enabling commercial applications.

Keywords:
DNA sequencingDNA translocationNanoporesSolid-state nanopores

More Related Videos

Monitoring Protein Adsorption with Solid-state Nanopores
08:51

Monitoring Protein Adsorption with Solid-state Nanopores

Published on: December 2, 2011

14.0K
Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution
11:55

Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution

Published on: August 16, 2016

12.0K

Related Experiment Videos

Last Updated: Dec 24, 2025

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
09:43

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores

Published on: October 31, 2013

14.0K
Monitoring Protein Adsorption with Solid-state Nanopores
08:51

Monitoring Protein Adsorption with Solid-state Nanopores

Published on: December 2, 2011

14.0K
Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution
11:55

Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution

Published on: August 16, 2016

12.0K

Area of Science:

  • Nanotechnology
  • Biotechnology
  • Genomics

Background:

  • Solid-state nanopores offer potential for DNA sequencing but lag behind bio-nanopores in performance.
  • Key limitations include low spatial resolution due to nanopore design and low temporal resolution from rapid DNA translocation.
  • Overcoming these challenges is crucial for commercializing nanopore DNA sequencing technology.

Purpose of the Study:

  • To review methods for enhancing spatial resolution in solid-state nanopores.
  • To focus on controllable techniques for improving temporal resolution by managing DNA translocation speed.
  • To provide insights into the future development of nanopore-based DNA sequencing.

Main Methods:

  • Summarizing existing strategies to improve spatial resolution in nanopore devices.
  • Analyzing methods for controlling the speed of DNA translocation through nanopores.
  • Discussing techniques to enhance the resolution of nanopore detection systems.

Main Results:

  • Spatial resolution can be improved by addressing nanopore length restrictions and surface properties.
  • Controlling DNA translocation speed significantly enhances temporal resolution and data acquisition.
  • Current methods offer pathways to overcome major limitations in solid-state nanopore sequencing.

Conclusions:

  • Solid-state nanopores require further development to match bio-nanopore performance for DNA sequencing.
  • Improving both spatial and temporal resolution is essential for practical applications.
  • Controlled DNA translocation is a critical factor for advancing nanopore sequencing technology.