Intact Cell Labeling

Intact cell labeling is a biological technique for marking molecules, structures, or cell populations without disrupting the cell membrane or overall cellular organization. It works by exposing living or preserved cells to selective probes, such as fluorescent dyes, antibodies, or affinity-based tags, that bind target components or enter cells under appropriate conditions; the resulting signal can then be detected by microscopy or other analytical methods. In biology, intact cell labeling supports visualization of cell morphology, localization of proteins and organelles, population identity, and cellular responses, helping researchers study cell function, interactions, development, and disease while preserving spatial context.

Intact Cell Labeling - Related Videos

Research

JoVE Journal - Biology

Single Cell Electroporation in vivo within the Intact Developing Brain

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Cited by 26 •

2008

Single-cell electroporation (SCE) is a specialized technique allowing delivery of DNA or other macromolecules into individual cells within intact tissue, including in vivo preparations. Here we detail the procedure for SCE of a fluorescent dye or plasmid DNA into neurons within the intact brain of the Xenopus laevis tadpole.

Research

JoVE Journal - Neuroscience
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Live-cell Imaging of Sensory Organ Precursor Cells in Intact Drosophila Pupae

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Cited by 27 •

2011

In this video, we describe a method for live cell imaging of asymmetrically dividing sensory organ progenitor cells and epidermal cells in intact Drosophila...

Single-cell Photoconversion in Living Intact Zebrafish

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Cited by 8 •

2018

Here, we present a protocol to show how cell photoconversion is achieved through UV exposure to specific areas expressing the fluorescent protein, Eos, in living animals.

Research

JoVE Journal - Neuroscience
Free Sample

Electrophysiological Characterization of GFP-Expressing Cell Populations in the Intact Retina

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Cited by 5 •

2011

This article depicts the recording of individual cells from fluorescently tagged neuronal populations in the intact mouse retina. By using two-photon infrared excitation transgenetically labeled cells were targeted for patch-clamp recording to study their light responses, receptive field properties, and morphology.

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy

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Cited by 23 •

2015

This protocol describes the labeling of epidermal growth factor receptor (EGFR) on COS7 fibroblast cells, and subsequent correlative light- and electron microscopy of whole cells in hydrated state. The label contained fluorescent quantum dots. The protocol can be used to study the stoichiometry of EGFR at the single molecule level.

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