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

Pathway tracing using biotinylated dextran amines.

A Reiner1, C L Veenman, L Medina

  • 1Department of Anatomy and Neurobiology, The University of Tennessee - Memphis, The Health Science Center, Memphis, TN 38163, USA. areiner@utmem.edu

Journal of Neuroscience Methods
|November 14, 2000
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

Therapeutic Apheresis Registry of the Spanish Society of Nephrology. Analysis of activity over the last five years.

Nefrologia·2026
Same author

A method for designing birdcage coils based on a simplified magnetic field model, validated experimentally at 4 T, 7 T, and 15.2 T.

HardwareX·2026
Same author

Leishmaniasis in Patients With Inflammatory Bowel Disease: A National Multicenter Study of GETECCU.

United European gastroenterology journal·2025
Same author

Rescue of BDNF expression by the thalamic parafascicular nucleus with chronic treatment with the mGluR2/3 agonist LY379268 may contribute to the LY379268 rescue of enkephalinergic striatal projection neurons in R6/2 Huntington's disease mice.

Neuroscience letters·2021
Same author

Remote RF excitation for small-bore MR imager at 15.2 T.

Journal of magnetic resonance (San Diego, Calif. : 1997)·2021
Same author

Agreements and uncertainties in autologous haematopoietic stem cell mobilization and collection. A Spanish consensus document.

Bone marrow transplantation·2019

Biotinylated dextran amines (BDA) are versatile tools for neural pathway tracing. Different molecular weights enable detailed anterograde or retrograde labeling, compatible with various visualization methods.

Area of Science:

  • Neuroscience
  • Neuroanatomy

Background:

  • Biotinylated dextran amines (BDA) are established tracers for neural circuit mapping.
  • Effective delivery methods include iontophoretic or pressure injection.

Purpose of the Study:

  • To highlight the versatility and applications of BDA in neural pathway tracing.
  • To detail the advantages of different BDA molecular weights for specific tracing needs.

Main Methods:

  • Utilizing high molecular weight BDA (10 k) for anterograde tracing of axons and terminals.
  • Employing low molecular weight BDA (3 k) for retrograde tracing of neuronal cell bodies.
  • Combining BDA tracing with avidin-biotinylated HRP (ABC) and diaminobenzidine (DAB) reactions for visualization.
  • Integrating BDA with electron microscopy (EM) fixation and processing.

Related Experiment Videos

  • Combining BDA with other tracers (e.g., PHA-L, cholera toxin B fragment, fluorescent dextran amines) for multi-modal labeling.
  • Main Results:

    • High molecular weight BDA provides sensitive and detailed labeling of axons and terminals.
    • Low molecular weight BDA offers sensitive and detailed retrograde labeling of neuronal cell bodies with Golgi-like resolution.
    • BDA is compatible with EM, allowing for ultrastructural studies.
    • BDA can be combined with other tracers for multi-color or multi-modal visualization.
    • BDA pathway tracing can be integrated with neurotransmitter immunolabeling.

    Conclusions:

    • BDA is a flexible and sensitive tool for both anterograde and retrograde neural pathway tracing.
    • Its compatibility with various visualization techniques and tracers enhances its utility in neuroscience research.
    • BDA facilitates detailed anatomical studies at both light and electron microscopic levels.