Nih/3t3 Cells

NIH/3T3 cells are an immortalized mouse embryonic fibroblast cell line widely used to study cell growth, signaling, and transformation in biology. Under adherent culture conditions, these cells attach to treated surfaces, proliferate in response to serum-derived signals, and typically show density-dependent growth inhibition as neighboring cells establish contact. Researchers use NIH/3T3 cells for transfection studies, wound-healing assays, oncogene and tumor-suppressor research, and evaluation of pathways that regulate proliferation and cytoskeletal organization. Their reproducible growth and well-characterized responses make them a practical model for investigating mammalian cell behavior and testing experimental methods before application to more specialized cell systems.

Nih/3t3 Cells - Related Videos

Research

JoVE Journal - Cancer Research
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Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells

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2025

This protocol describes the in vivo reprogramming of mouse cancer cells into type 1 dendritic-like cells within the tumor microenvironment through enforced expression of the transcription factors PU.1, IRF8, and BATF3.

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JoVE Journal - Biology

Derivation of Hematopoietic Stem Cells from Murine Embryonic Stem Cells

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Cited by 8 •

2007

This protocol details the derivation of transplantable hematopoietic stem cells from mouse embryonic stem cells (ESC) and their subsequent injection into lethally irradiated recipient mice. Briefly, ESC are differentiated as embryoid bodies, which are then infected with retroviral HoxB4 and co-cultured with OP9 stromal cells and hematopoietic cytokines.

Human ES cells: Starting Culture from Frozen Cells

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2006

Here we demonstrate how our lab begins a HuES human embryonic stem cell line culture from a frozen stock.

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations

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Cited by 2 •

2012

Metaphase to anaphase transition is triggered through anaphase-promoting complex (APC/C)-dependent ubiquitination and subsequent destruction of cyclin B. Here, we established a system which, following pulse-chase labeling, allows monitoring cyclin B proteolysis in entire cell populations and facilitates the detection of interference by the mitotic checkpoint.

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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...

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