Live Cell Labeling

Live cell labeling is the process of marking living cells or their components so researchers can track identity, location, behavior, or function over time. Labels may use membrane-permeable fluorescent dyes, antibody conjugates, nanoparticles, or genetically encoded reporters that bind target molecules or produce signals in response to cellular conditions while preserving cell viability. In bioengineering, these approaches support real-time imaging, cell sorting, lineage tracking, and evaluation of engineered tissues, biomaterials, and cell-based therapies. Careful selection of label chemistry, delivery method, signal stability, and cytotoxicity helps produce reliable measurements without substantially altering normal cell behavior.

Live Cell Labeling - Related Videos

Research

JoVE Journal - Neuroscience

Differential Labeling of Cell-surface and Internalized Proteins after Antibody Feeding of Live Cultured Neurons

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Cited by 24 •

2014

We describe a method to label protein on the surface of living neurons using a specific polyclonal antibody to extracellular epitopes. Protein bound by the antibody on the cell surface and subsequently internalized via endocytosis can be distinguished from protein remaining on, or trafficked to, the surface during the incubation.

Research

JoVE Journal - Biology
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Live Imaging of GFP-labeled Proteins in Drosophila Oocytes

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Cited by 5 •

2013

A protocol for live imaging of GFP-tagged proteins or autofluorescent structures in individual Drosophila oocytes is described.

Research

JoVE Journal - Biology
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Fluorescent Labeling of COS-7 Expressing SNAP-tag Fusion Proteins for Live Cell Imaging

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Cited by 8 •

2010

SNAP-tag and CLIP-tag protein labeling systems enable the specific, covalent attachment of molecules, including fluorescent dyes, to a protein of interest in live cells. Once cloned and expressed, the tagged protein can be used with a variety of substrates for numerous downstream applications without having to clone again.

Identification of Small Molecule-binding Proteins in a Native Cellular Environment by Live-cell Photoaffinity Labeling

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Cited by 4 •

2016

We describe here a method for identification of small molecule-binding proteins using photoaffinity labeling. The advantage of this technique is that binding and covalent labeling of the target proteins occurs within the live cellular environment, removing the risk of disrupting native protein structure and binding conditions upon cell lysis.

Research

JoVE Journal - Biology
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Detection of Intracellular Gene Expression in Live Cells of Murine, Human and Porcine Origin Using Fluorescence-labeled Nanoparticles

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Cited by 1 •

2015

This manuscript describes a novel technique which allows the detection of intracellular gene expression after endocytosis of fluorescence-labeled nanoparticles directly in live cells. The method does not require manipulation of the cells and is not restricted with respect to the target gene or species.

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