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

Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

28.6K
Stem cells are undifferentiated cells that divide and produce different types of cells. Ordinarily, cells that have differentiated into a specific cell type are post-mitotic—that is, they no longer divide. However, scientists have found a way to reprogram these mature cells so that they “de-differentiate” and return to an unspecialized, proliferative state. These cells are also pluripotent like embryonic stem cells—able to produce all cell types—and are therefore...
28.6K
Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

4.0K
4.0K
Induced Pluripotent Stem Cells01:06

Induced Pluripotent Stem Cells

6.2K
Stem cells are undifferentiated cells that divide and produce different cell types. Ordinarily, cells that have differentiated into a specific cell type are terminally differentiated; however, scientists have found a way to reprogram these mature cells so that they dedifferentiate and return to an unspecialized, proliferative state. These cells are pluripotent like embryonic stem cells—able to produce all cell types—and are called induced pluripotent stem cells (iPSCs).
Somatic...
6.2K
Labeling DNA Probes03:31

Labeling DNA Probes

9.7K
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
9.7K

You might also read

Related Articles

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

Sort by
Same author

Dual-readout villus-like scaffold microfluidic platform for quantitative analysis of gut microbiota formation under perfusion.

The Analyst·2026
Same author

Habitat-Associated Dietary Plasticity in the Japanese Weasel (<i>Mustela itatsi</i>): Fecal Analysis in a Floodplain Wetland and Comparative Synthesis.

Animals : an open access journal from MDPI·2026
Same author

Acute Appendicitis With Periappendiceal Abscess Caused by Migration of an Endoscopic Clip Into the Appendix: A Case Report.

Cureus·2026
Same author

Impact-shear-induced millisecond clustering during shear melting of colloidal crystals.

Communications chemistry·2026
Same author

Design and Synthesis of Chiral Macrocycles Consisting of Azobenzene Units That Undergo Asymmetric Photochemical and Thermal Isomerization.

The Journal of organic chemistry·2026
Same author

Consecutive Mechano-Immunophenotyping of Single Cells in a Photopatterned Microfluidic Channel.

ACS omega·2026

Related Experiment Video

Updated: Mar 26, 2026

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging
07:42

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging

Published on: April 2, 2008

13.9K

Induced Pluripotent Stem Cell Labeling Using Quantum Dots.

Hiroshi Yukawa1, Kaoru Suzuki1, Yuki Kano2

  • 1FIRST Research Center for Innovative Nanobiodevices, Nagoya University , Furo-cho, Chikusa-ku, Nagoya , Japan.

Cell Medicine
|February 10, 2016
PubMed
Summary

Quantum dots (QDs) can label induced pluripotent stem (iPS) cells for cell tracking in regenerative medicine. Combining QDs with cell-penetrating peptides like octaarginine (R8) enabled effective, non-toxic labeling of iPS cells without affecting their pluripotency.

Keywords:
Induced pluripotent stem (iPS) cellsOctaarginine (R8)Quantum dots (QDs)

More Related Videos

Production and Targeting of Monovalent Quantum Dots
10:16

Production and Targeting of Monovalent Quantum Dots

Published on: October 23, 2014

26.1K
Generation and Labeling of Murine Bone Marrow-derived Dendritic Cells with Qdot Nanocrystals for Tracking Studies
07:34

Generation and Labeling of Murine Bone Marrow-derived Dendritic Cells with Qdot Nanocrystals for Tracking Studies

Published on: June 2, 2011

25.4K

Related Experiment Videos

Last Updated: Mar 26, 2026

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging
07:42

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging

Published on: April 2, 2008

13.9K
Production and Targeting of Monovalent Quantum Dots
10:16

Production and Targeting of Monovalent Quantum Dots

Published on: October 23, 2014

26.1K
Generation and Labeling of Murine Bone Marrow-derived Dendritic Cells with Qdot Nanocrystals for Tracking Studies
07:34

Generation and Labeling of Murine Bone Marrow-derived Dendritic Cells with Qdot Nanocrystals for Tracking Studies

Published on: June 2, 2011

25.4K

Area of Science:

  • Regenerative Medicine
  • Stem Cell Biology
  • Nanotechnology

Background:

  • Induced pluripotent stem (iPS) cells are crucial for regenerative medicine and stem cell therapy.
  • Effective cell tracing methods are essential for monitoring transplanted cells in clinical applications.
  • Traditional labeling probes have limitations, necessitating novel approaches.

Purpose of the Study:

  • To evaluate quantum dots (QDs) as fluorescent labeling materials for iPS cells.
  • To assess the cytotoxicity and impact of QD labeling on iPS cell pluripotency and differentiation state.
  • To determine the optimal conditions for labeling iPS cells using QDs.

Main Methods:

  • iPS cells were incubated with quantum dots (QDs) alone and in combination with cell-penetrating peptides, specifically octaarginine (R8).
  • Cytotoxicity assays were performed to assess the viability of QD-labeled iPS cells.
  • Pluripotency and undifferentiated state of labeled iPS cells were evaluated using standard stem cell assays.

Main Results:

  • Direct labeling of iPS cells with QDs alone was ineffective.
  • Co-incubation with octaarginine (R8) enabled efficient fluorescence labeling of iPS cells with QDs.
  • No significant cytotoxicity was observed at QD concentrations up to 8 nM.
  • QD-labeled iPS cells retained their undifferentiated state and pluripotency.

Conclusions:

  • Quantum dots, when conjugated with cell-penetrating peptides like R8, are suitable for non-toxic fluorescence labeling of iPS cells.
  • This labeling method allows for effective tracing of transplanted iPS cells in regenerative medicine applications.
  • QD labeling preserves the critical characteristics of iPS cells, including pluripotency.