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

Techniques for using antisense oligodeoxyribonucleotides to study gene expression.

C J Marcus-Sekura1

  • 1Division of Virology, Food and Drug Administration, Bethesda, Maryland 20892.

Analytical Biochemistry
|August 1, 1988
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

Generation of HIV-1/HIV-2 cross-reactive peptide antisera by small sequence changes in HIV-1 reverse transcriptase and integrase immunizing peptides.

Journal of biomedical science·1998
Same author

Susceptibility of the Sf9 insect cell line to infection with adventitious viruses.

Biologicals : journal of the International Association of Biological Standardization·1994
Same author

Regulatory issues relating to the use of recombinant vectors in production of human vaccines.

Developments in biological standardization·1994
Same author

Conformation-dependent recognition of baculovirus-expressed Epstein-Barr virus gp350 by a panel of monoclonal antibodies.

The Journal of general virology·1993
Same author

St Louis encephalitis virus establishes a productive, cytopathic and persistent infection of Sf9 cells.

The Journal of general virology·1993
Same author

Characterization of a DNA binding domain in the C-terminus of HIV-1 integrase by deletion mutagenesis.

Nucleic acids research·1993
Same journal

Lysozyme assay using a rationally designed GN4G2 substrate with coupled β-glucosidase reaction.

Analytical biochemistry·2026
Same journal

The long run: A tribute to Arthur Joseph Lawrence Cooper.

Analytical biochemistry·2026
Same journal

Evaluation of a method for affinity measurement using solution equilibrium titration with magnetic beads.

Analytical biochemistry·2026
Same journal

Metabolomics approach using UHPLC/QE-MS for the mechanism of He Xue Ming Mu tablets on non-proliferative diabetic retinopathy.

Analytical biochemistry·2026
Same journal

UniRES-GO: Unified residue-level early fusion of sequence and predicted structure for protein function prediction.

Analytical biochemistry·2026
Same journal

IgG detection by enzyme-linked mass spectrometric assay versus color, fluorescent, ECL in buffer and serum.

Analytical biochemistry·2026
See all related articles

Antisense oligonucleotides offer a powerful method for studying gene function by inhibiting gene expression. These short DNA sequences are practical tools for molecular biology research in various systems.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Assigning functions to DNA sequences and regulating gene expression are key challenges in molecular biology.
  • Classical genetic mutant approaches are limited in eukaryotic systems.
  • Antisense oligonucleotides provide a promising alternative for gene function studies.

Purpose of the Study:

  • To review the practical applications of antisense oligodeoxyribonucleotides in biological systems.
  • To highlight the advantages of short oligodeoxyribonucleotides over antisense RNA.
  • To introduce methods for studying gene expression and regulation.

Main Methods:

  • Introduction of antisense oligodeoxyribonucleotides into in vitro assays or tissue culture systems.
  • Utilizing nucleotide sequences complementary to sense DNA sequences.

Related Experiment Videos

  • Employing hybridization arrest of translation to inhibit gene expression.
  • Main Results:

    • Antisense oligonucleotides effectively inhibit gene expression.
    • Short oligodeoxyribonucleotides demonstrate stability and synthetic advantages.
    • Increased availability of sequence data and automated synthesis enhance practicality.

    Conclusions:

    • Antisense oligodeoxyribonucleotides are valuable tools for investigating gene function and regulation.
    • Their utility in in vitro and tissue culture assays is well-demonstrated.
    • Advances in sequencing and synthesis make antisense oligodeoxyribonucleotide studies more accessible.