Cal-62 Cell Line

The Cal-62 cell line is a human cancer cell model derived from anaplastic thyroid carcinoma, an aggressive form of thyroid cancer, and is used to investigate malignant cell behavior in vitro. Researchers maintain Cal-62 cells under controlled culture conditions, where they proliferate as a relatively uniform population that can be experimentally exposed to genetic, molecular, or pharmacological perturbations. This model supports studies of thyroid cancer signaling, tumor-cell growth, survival, invasion, and responses to candidate treatments. By providing a reproducible system for comparing untreated and experimentally modified cells, Cal-62 contributes to cancer biology research, therapeutic screening, and the evaluation of mechanisms underlying aggressive disease.

Cal-62 Cell Line - Related Videos

Research

JoVE Journal - Cancer Research

Assessing Cell Viability and Death in 3D Spheroid Cultures of Cancer Cells

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Cited by 34 •

2019

Here, we present several simple methods for evaluating viability and death in 3D cancer cell spheroids, which mimic the physico-chemical gradients of in vivo tumors much better than the 2D culture. The spheroid model, therefore, allows evaluation of the cancer drug efficacy with improved translation to in vivo conditions.

Measuring Calpain Activity in Fixed and Living Cells by Flow Cytometry

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Cited by 6 •

2010

This article will detail the protocol for measuring calpain activity in fixed and living cells using flow cytometry.

Research

JoVE Journal - Immunology and Infection
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Preparation and Use of HIV-1 Infected Primary CD4+ T-Cells as Target Cells in Natural Killer Cell Cytotoxic Assays

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Cited by 12 •

2011

Cytotoxicity assays to measure natural killer cell lytic responses to HIV-infected cells is limited by the purity of the target cells. We demonstrate here the isolation of a highly purified population of HIV-1 infected primary T-cell blasts by taking advantage of HIV-1 s ability to down-modulate CD4.

Determination of Immune Cell Identity and Purity Using Epigenetic-Based Quantitative PCR

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Cited by 1 •

2020

Here we describe a robust method of determining immune cell identity and purity through epigenetic signatures detected using quantitative PCR (qPCR). DNA demethylation at a specific locus serves as a unique identifier for a particular cell type and allows for identification of CD8+, regulatory, or Th17 T cells.

Imaging Local Ca2+ Signals in Cultured Mammalian Cells

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Cited by 17 •

2015

Here we present techniques for imaging local IP3-mediated Ca2+ events using fluorescence microscopy in intact mammalian cells loaded with Ca2+ indicators together with an algorithm that automates identification and analysis of these events.

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