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

RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...
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.

You might also read

Related Articles

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

Sort by
Same author

DNA methylation mediates the multiple sclerosis onset risk associated with HHV-6 DNA positivity.

Environmental epigenetics·2026
Same author

Real-time, multi-pathogen wastewater genomic surveillance with Freyja 2.

medRxiv : the preprint server for health sciences·2025
Same author

A systematic review and meta-analysis on gene-environment interaction effects on the associations of vitamin D and sun exposure with multiple sclerosis risk.

Multiple sclerosis and related disorders·2025
Same author

Publisher Correction: Ultra-high gradient connectomics and microstructure MRI scanner for imaging of human brain circuits across scales.

Nature biomedical engineering·2025
Same author

Ultra-high gradient connectomics and microstructure MRI scanner for imaging of human brain circuits across scales.

Nature biomedical engineering·2025
Same author

Genomics reveals zoonotic and sustained human mpox spread in West Africa.

Nature·2025
Same journal

Isolation of Mesenchymal Stem Cell-Derived Extracellular Vesicles.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Modeling Melanoma Immune Surveillance by CAR-T Cells in Human Skin Organoids.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Stepwise Optimization of a Matrigel-Based In Vitro Angiogenesis Assay for Reproducible and Quantifiable 2D-Tube Formation Using HUVECs.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Quantifying Mechanical Properties of Fresh Ovarian Tissue with Optical Brillouin Microscopy.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

3D Chromatin Architecture During Early Development: New Methods and New Findings.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Metabolic Plasticity in Embryogenesis Throughout the Lens of NAD<sup></sup>.

Methods in molecular biology (Clifton, N.J.)·2026
See all related articles

Related Experiment Video

Updated: Jun 7, 2026

Linear Amplification Mediated PCR &#8211; Localization of Genetic Elements and Characterization of Unknown Flanking DNA
11:58

Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA

Published on: June 25, 2014

Lariat-dependent nested PCR for flanking sequence determination.

Daniel J Park1

  • 1Genetic Epidemiology Laboratory, Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia. djp@unimelb.edu.au

Methods in Molecular Biology (Clifton, N.J.)
|October 23, 2010
PubMed
Summary
This summary is machine-generated.

Lariat-dependent Nested (LaNe) PCR offers a streamlined method for identifying unknown DNA or RNA sequences adjacent to known regions. This technique simplifies complex protocols by avoiding extensive enzyme preprocessing steps.

More Related Videos

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR
10:54

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR

Published on: July 27, 2019

Detecting the Lyme Disease Spirochete, Borrelia Burgdorferi, in Ticks Using Nested PCR
07:20

Detecting the Lyme Disease Spirochete, Borrelia Burgdorferi, in Ticks Using Nested PCR

Published on: February 4, 2018

Related Experiment Videos

Last Updated: Jun 7, 2026

Linear Amplification Mediated PCR &#8211; Localization of Genetic Elements and Characterization of Unknown Flanking DNA
11:58

Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA

Published on: June 25, 2014

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR
10:54

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR

Published on: July 27, 2019

Detecting the Lyme Disease Spirochete, Borrelia Burgdorferi, in Ticks Using Nested PCR
07:20

Detecting the Lyme Disease Spirochete, Borrelia Burgdorferi, in Ticks Using Nested PCR

Published on: February 4, 2018

Area of Science:

  • Molecular Biology
  • Genomics
  • Biotechnology

Background:

  • Characterizing unknown flanking DNA or RNA sequences is crucial in molecular biology.
  • Existing methods for determining flanking sequences often suffer from poor resolution, experimental failure, or complex handling procedures.

Purpose of the Study:

  • To present Lariat-dependent Nested (LaNe) PCR as an effective method for sequencing unknown flanking DNA or RNA.
  • To offer a simplified alternative to existing, more complex methods for sequence determination.

Main Methods:

  • Utilizes Lariat-dependent Nested (LaNe) PCR, a two-sided gene-specific polymerase chain reaction (PCR) approach.
  • Incorporates optional nesting for enhanced resolution.
  • Eliminates the need for cumbersome and inefficient enzyme preprocessing steps.

Main Results:

  • LaNe PCR provides a robust strategy for characterizing unknown flanking sequences.
  • The method is designed to overcome limitations of resolution and complexity associated with other techniques.

Conclusions:

  • Lariat-dependent Nested (LaNe) PCR is a valuable tool for researchers needing to identify adjacent DNA or RNA sequences.
  • This method offers a more efficient and user-friendly approach to sequence characterization.