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

An easy method for impaling cells using the micromanipulation technique.

A L Perez-Samartin1, L Martinez-Millan, F Doñate-Oliver

  • 1Department of Neurosciences, Universidad del País Vasco, Leioa, Spain.

Journal of Neuroscience Methods
|May 1, 1990
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

Docosahexaenoic Acid Reduces Cerebral Damage and Ameliorates Long-Term Cognitive Impairments Caused by Neonatal Hypoxia-Ischemia in Rats.

Molecular neurobiology·2016
Same author

Functional and morphological characterization of glutamate transporters in the rat locus coeruleus.

British journal of pharmacology·2013
Same author

Somatosensory cross-modal plasticity in the superior colliculus of visually deafferented rats.

Neuroscience·2009
Same author

Long-range correlations in rabbit brain neural activity.

Annals of biomedical engineering·2006
Same author

Immunocytochemical localization of metabotropic (mGluR2/3 and mGluR4a) and ionotropic (GluR2/3) glutamate receptors in adrenal medullary ganglion cells.

Histology and histopathology·2005
Same author

Immunoreactivity for the group III receptor subtype mGluR4a in the visual layers of the rat superior colliculus.

Neuroscience·2005

This study introduces a novel microscope design for easier neuron filling. The simultaneous displacement of the microscope head and micromanipulator simplifies intracellular iontophoresis injection of Lucifer yellow in brain slices.

Area of Science:

  • Neuroscience
  • Microscopy techniques
  • Cell biology

Background:

  • Intracellular injection techniques are crucial for neuroscience research.
  • Filling neurons, particularly in brain slices, presents technical challenges.
  • Current methods may lack precision or ease of use.

Purpose of the Study:

  • To describe a new method for improving intracellular injection.
  • To facilitate the filling of neurons in brain slices using iontophoresis.
  • To enhance the ease and efficiency of Lucifer yellow filling.

Main Methods:

  • A fixed-stage microscope with an attached micromanipulator was utilized.
  • Simultaneous displacement of the microscope head and micromanipulator during focusing was implemented.

Related Experiment Videos

  • Axial displacement of the microscope towards the target cell was enabled.
  • Main Results:

    • The described method simplifies the process of neuron filling.
    • Intracellular iontophoresis injection of Lucifer yellow into neurons in brain slices became considerably easier.
    • The simultaneous movement design enhances precision and accessibility.

    Conclusions:

    • The novel microscope design offers a significant improvement for neuron injection.
    • This technique facilitates detailed study of neuronal morphology and function.
    • The method is particularly beneficial for experiments requiring precise intracellular labeling.