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

Immunocytochemistry and Immunohistochemistry01:22

Immunocytochemistry and Immunohistochemistry

Immunocytochemistry (ICC) and immunohistochemistry (IHC) are techniques that use antibodies to check for specific proteins or antigens in a sample. The technique was first published by Albert Coons in 1941 to detect the presence of pneumococcal antigen in tissue sections from mice infected with Pneumococcus. Immunocytochemistry helps localization of proteins or antigens in individual cells like blood cells, stem cells, etc., while immunohistochemistry does the same for tissue samples.
These...
Immunofluorescence Microscopy01:12

Immunofluorescence Microscopy

A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
The...
Fixation and Sectioning01:03

Fixation and Sectioning

Two basic types of preparation are used to visualize specimens with a light microscope: wet mounts and fixed specimens.
The simplest type of preparation is the wet mount, in which the specimen is placed in a drop of liquid on the slide. A liquid specimen can be directly deposited on the slide using a dropper. Solid specimens, such as skin scraping, can be placed on the slide before adding a drop of liquid to prepare the wet mount. Sometimes the liquid is simply water, but stains are often added...
Immunogold Electron Microscopy01:20

Immunogold Electron Microscopy

Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.

You might also read

Related Articles

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

Sort by
Same author

Clinical performance of the HPV-Risk assay on cervical samples in SurePath medium using the VALGENT-4 panel.

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology·2019
Same author

High-grade cervical intraepithelial neoplasia in human papillomavirus self-sampling of screening non-attenders.

British journal of cancer·2017
Same author

Prevalence of Human Papillomavirus in Self-Taken Samples from Screening Nonattenders.

Journal of clinical microbiology·2017
Same author

Clinical and microbiological features of Actinotignum bacteremia: a retrospective observational study of 57 cases.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology·2016
Same author

Thalamic infarcts: Effects on cerebral blood flow, metabolism, and neuropsychological function.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association·2015
Same author

Analysis of a theoretical model for anisotropic enzyme membranes application to enzyme electrodes.

Applied biochemistry and biotechnology·2013

Related Experiment Video

Updated: Jun 12, 2026

Impression Cytology of the Lid Wiper Area
07:01

Impression Cytology of the Lid Wiper Area

Published on: August 9, 2016

Control specimens for immunocytochemistry in liquid-based cytology.

T Hansen1, H Pedersen, V Brauner

  • 1Department of Pathology, Sygehus Sønderjylland, Sønderborg, Denmark. tovelhansen@gmail.com

Cytopathology : Official Journal of the British Society for Clinical Cytology
|May 21, 2010
PubMed
Summary

Developing control specimens for immunocytochemistry (ICC) using liquid-based cytology (LBC) is now feasible. Fresh tissue and body fluid samples can be processed into slides and stored for at least 40 days without losing antigenicity.

More Related Videos

Simple Detection of Primary Cilia by Immunofluorescence
08:07

Simple Detection of Primary Cilia by Immunofluorescence

Published on: May 15, 2020

Related Experiment Videos

Last Updated: Jun 12, 2026

Impression Cytology of the Lid Wiper Area
07:01

Impression Cytology of the Lid Wiper Area

Published on: August 9, 2016

Simple Detection of Primary Cilia by Immunofluorescence
08:07

Simple Detection of Primary Cilia by Immunofluorescence

Published on: May 15, 2020

Area of Science:

  • Cytopathology
  • Immunohistochemistry
  • Molecular Diagnostics

Background:

  • Immunohistochemistry (IHC) controls are standard, but suitable immunocytochemistry (ICC) controls are challenging to establish.
  • Existing literature lacks comprehensive methods for preparing ICC control specimens.

Purpose of the Study:

  • To develop and validate a method for selecting, collecting, processing, and storing control specimens for ICC using liquid-based cytology (LBC).

Main Methods:

  • Utilized 21 antibodies targeting cellular components from tonsils, serous fluids, and bronchial washings.
  • Collected tonsil specimens via brushing into SurePath™ vials; fixed serous fluids and bronchial washings in CytoRich Red™.
  • Prepared unstained SurePath™ slides, stored them at 5°C for up to 40 days, and performed ICC.

Main Results:

  • Unstained SurePath™ slides demonstrated positive reactivity with relevant antibodies.
  • Stored slides maintained staining intensity for up to 40 days, indicating preserved antigenicity.

Conclusions:

  • Body fluid and cell-suspension specimens from fresh tissues are effective as ICC controls, individually or as mixtures.
  • Dry, unstained slides can be stored refrigerated for at least 40 days without compromising antigenicity for ICC.