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

DAPI as a useful stain for nuclear quantitation.

B I Tarnowski1, F G Spinale, J H Nicholson

  • 1Department of Pathology, Medical University of South Carolina, Charleston 29425.

Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission
|January 1, 1991
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

Myocardial extracellular matrix remodeling with the development of pacing induced congestive heart failure contributory mechanisms.

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology·2015
Same author

The effect of neuromuscular blockade on mask ventilation.

Anaesthesia·2011
Same author

Use of sulfadiazine in presence of hematuria.

The New England journal of medicine·2010
Same author

Some unusual findings in an epidemic of anterior poliomyelitis.

The New England journal of medicine·2010
Same author

Amebiasis.

The New England journal of medicine·2010
Same author

Contributory role of matrix metalloproteinases in cardiovascular remodeling.

Current drug targets. Cardiovascular & haematological disorders·2003
Same journal

Relationship between mast cell density and microvascular density with pathological features in canine mammary gland carcinomas.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
Same journal

Xiaokeping combined with low-carbohydrate diet slows cognitive decline in diabetic rats through activating TGF-β1/Smad7 signaling.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
Same journal

Sequential multi-organ preparation of rat liver and kidney precision-cut tissue slices: impact of collection method, anatomical region, and processing time on ATP-based viability.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
Same journal

Stains recently certified.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
Same journal

Stains recently certified.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
Same journal

Stains recently certified.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026
See all related articles

4

Area of Science:

  • Cell Biology
  • Microscopy

Background:

  • Nuclear DNA visualization is crucial for cell studies.
  • Accurate cell counting and morphology assessment are vital.

Purpose of the Study:

  • To evaluate 4',6-diamidino-2-phenylindole (DAPI) as a nuclear stain for light and electron microscopy.
  • To assess the impact of DAPI staining on cellular ultrastructure and its utility for multiple analyses.

Main Methods:

  • Cells were stained with DAPI for nuclear visualization.
  • Light microscopy was used to count nuclei and assess cell morphology.
  • Stained cells were subsequently processed for electron microscopy to examine ultrastructure.

Main Results:

  • DAPI effectively stained nuclear DNA in both living and fixed cells.

Related Experiment Videos

  • DAPI staining allowed for accurate nucleus counting and gross cell morphology assessment.
  • No ultrastructural alterations were observed in DAPI-stained cells compared to unstained controls.
  • Conclusions:

    • DAPI is a reliable and simple fluorescent stain for nuclear DNA.
    • DAPI staining does not induce ultrastructural damage, enabling sequential light and electron microscopy.
    • This method permits multiple analyses on the same cell sample, reducing the need for duplicates.