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Related Experiment Video

Updated: Jun 16, 2026

Retrograde Loading of Nerves, Tracts, and Spinal Roots with Fluorescent Dyes
06:47

Retrograde Loading of Nerves, Tracts, and Spinal Roots with Fluorescent Dyes

Published on: April 19, 2012

Dye loading with patch pipettes.

Jens Eilers, Arthur Konnerth

    Cold Spring Harbor Protocols
    |February 12, 2010
    PubMed
    Summary
    This summary is machine-generated.

    This protocol details loading single cells with fluorescent probes using patch pipettes. This versatile method enables combined electrophysiological and optical measurements for various cell studies.

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    Area of Science:

    • Neuroscience
    • Cell Biology
    • Biophysics

    Background:

    • Patch-clamp technique is established for single-cell electrophysiology.
    • Fluorescent probes are crucial for visualizing cellular processes.
    • Combining electrophysiology with optical measurements offers deeper insights.

    Purpose of the Study:

    • To describe a protocol for loading individual cells with fluorescent probes using patch pipettes.
    • To highlight the versatility of this technique for various cell types and applications.
    • To emphasize the combined electrophysiological and optical measurement capabilities.

    Main Methods:

    • Utilizing whole-cell patch-clamp recordings for dye loading.
    • Employing patch pipettes for precise delivery of fluorescent probes into single cells.

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    Last Updated: Jun 16, 2026

    Retrograde Loading of Nerves, Tracts, and Spinal Roots with Fluorescent Dyes
    06:47

    Retrograde Loading of Nerves, Tracts, and Spinal Roots with Fluorescent Dyes

    Published on: April 19, 2012

    Imaging Exocytosis in Retinal Bipolar Cells with TIRF Microscopy
    11:54

    Imaging Exocytosis in Retinal Bipolar Cells with TIRF Microscopy

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    Published on: June 20, 2018

  • Applying a broad range of fluorescent dyes suitable for patch-clamp loading.
  • Main Results:

    • Successful single-cell dye labeling in cultured neurons, brain slices, and in vivo preparations.
    • Demonstrated suitability of various dyes, including morphological markers, ion indicators, and FRET/FCS/FRAP probes.
    • Established Ca(2+) imaging as a primary application.

    Conclusions:

    • Whole-cell patch-clamp recording is a versatile technique for single-cell fluorescent probe loading.
    • This method facilitates combined electrophysiological and quantitative optical measurements.
    • The protocol supports diverse applications in cell biology and neuroscience research.