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

Lymphocyte proliferation and cytotoxic assays using flat-bed scintillation counting.

C G Potter1, F Gotch, G T Warner

  • 1Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Headington, Oxford, U.K.

Journal of Immunological Methods
|December 24, 1987
PubMed
Summary

This study demonstrates a flat-bed scintillation counter for lymphocyte assays. It offers efficient, reproducible measurement of radioactivity in chromium-51 (51Cr) release and tritium ([3H]) thymidine uptake assays.

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

Minimum Detectable Intakes and Doses for Uranium Bioassays-Comparison between Alpha Spectrometry and ICP-MS.

Health physics·2024
Same author

Dysregulated immunophenotypic attributes of plasmacytoid but not myeloid dendritic cells in HIV-1 infected individuals in the absence of highly active anti-retroviral therapy.

Clinical and experimental immunology·2012
Same author

Amplified antigen-specific immune responses in HIV-1 infected individuals in a double blind DNA immunization and therapy interruption trial.

Vaccine·2011
Same author

Programmed death (PD)-1 molecule and its ligand PD-L1 distribution among memory CD4 and CD8 T cell subsets in human immunodeficiency virus-1-infected individuals.

Clinical and experimental immunology·2009
Same author

Lessons from IAVI-006, a phase I clinical trial to evaluate the safety and immunogenicity of the pTHr.HIVA DNA and MVA.HIVA vaccines in a prime-boost strategy to induce HIV-1 specific T-cell responses in healthy volunteers.

Vaccine·2008
Same author

A mathematical model comparing solute kinetics in low- and high-BMI hemodialysis patients.

The International journal of artificial organs·2007

Area of Science:

  • Immunology
  • Biotechnology
  • Radiochemistry

Background:

  • Lymphocyte proliferation and cytotoxicity assays are crucial in immunological research.
  • Accurate and efficient measurement of radioactivity is essential for these assays, specifically for chromium-51 (51Cr) release and tritium ([3H]) thymidine uptake.
  • Traditional methods may face limitations in throughput and sensitivity.

Purpose of the Study:

  • To evaluate a flat-bed scintillation counter for measuring radioactivity in lymphocyte assays.
  • To assess the efficiency, linearity, and reproducibility of the counter for 51Cr release and [3H]thymidine uptake assays.
  • To determine the potential for increased assay sensitivity and cost-effectiveness.

Main Methods:

  • Lymphocyte samples labeled with 51Cr or [3H]thymidine were prepared on glass fibre filters.

Related Experiment Videos

  • Radioactivity was measured using a flat-bed scintillation counter, processing up to 96 samples simultaneously without removal.
  • Assay linearity, reproducibility (coefficient of variation), background, and efficiency were analyzed.
  • Main Results:

    • The flat-bed scintillation counter demonstrated good linearity between count rate and the amount of radioactive material on filters for both assay types.
    • High reproducibility was achieved, with a coefficient of variation within 5% for 96 samples.
    • The counter's low background and high efficiency led to increased assay sensitivity and potential material cost savings.

    Conclusions:

    • The evaluated flat-bed scintillation counter provides a sensitive, reproducible, and efficient method for quantifying radioactivity in lymphocyte 51Cr release and [3H]thymidine uptake assays.
    • This technology allows for rapid sample processing and offers significant advantages in terms of assay sensitivity and cost-effectiveness.
    • Commercial versions with multiple counting heads further enhance sample throughput for high-volume research.