Trex 293 Cells

T-REx 293 cells are a genetically engineered human embryonic kidney cell line designed for tetracycline-regulated gene expression, providing a controlled system for studying gene function and producing recombinant proteins. These cells constitutively express the tetracycline repressor protein, which binds tetracycline operator sequences and suppresses a linked transgene promoter until tetracycline or doxycycline causes repressor release, enabling inducible expression. In genetics research, the system supports transient or stable introduction of constructs, analysis of dosage- and time-dependent phenotypes, and functional testing of proteins or variants while limiting potentially harmful expression before induction. Its tunable regulation improves experimental control in mammalian cell studies.

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JoVE Journal - Immunology and Infection
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Cited by 49 •

2011

A rapid, simple and cost-effective protocol for the generation of donor-derived multivirus-specific CTLs (rCTL) for infusion to allogeneic hematopoietic stem cell transplant (HSCT) recipients at risk of developing CMV, Adv or EBV infections. This manufacturing process is GMP-compliant and should ensure the broader implementation of T-cell immunotherapy beyond specialized centers.

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JoVE Journal - Biology
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2023

Zebrafish targeting reactive electrophiles and oxidants (Z-REX) is a chemical biology-based method for the investigation of reactive small-molecule signaling. This technique can be applied to live fish of different developmental stages. Here, we couple standard assays in zebrafish with Z-REX for signaling pathway analysis.

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JoVE Journal - Cancer Research

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2025

Given the limited xenograft models available to study interactions between human CART and myeloid cells, we established in vitro and in vivo models to understand the impacts of human macrophages on CART cells. Findings can potentially be generalized to evaluate macrophage roles in the tumor microenvironment and test macrophage-targeted immunotherapies.

Selection-dependent and Independent Generation of CRISPR/Cas9-mediated Gene Knockouts in Mammalian Cells

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Cited by 6 •

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Recent advances in the ability to genetically manipulate somatic cell lines hold great potential for basic and applied research. Here, we present two approaches for CRISPR/Cas9 generated knockout production and screening in mammalian cell lines, with and without the use of selectable markers.

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JoVE Journal - Biology
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Transfecting and Nucleofecting Human Induced Pluripotent Stem Cells

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Cited by 26 •

2011

Despite recent advancements in genetic modification, transfection of human embryonic stem cells (HESCs) remains a capricious process. To our knowledge, systematic and efficient methods to transfect human induced pluripotent stem cells (iPSCs) have not been reported. Here, we describe robust protocols to efficiently transfect and nucleofect human iPSCs.

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