Nucleofector System

The Nucleofector System is an electroporation-based technology that introduces DNA, RNA, or other molecules directly into cells, including primary and hard-to-transfect cell types. It combines cell-specific solutions with precisely controlled electrical pulses that temporarily permeabilize the plasma and, in some protocols, nuclear membranes, allowing genetic material to enter while supporting cell recovery. In immunology and infection research, the system enables manipulation of T cells, B cells, macrophages, dendritic cells, and other immune populations for gene function studies, reporter assays, antiviral research, and the development of engineered cellular models. Its efficiency can improve experiments where conventional transfection methods perform poorly.

Nucleofector System - Related Videos

Research

JoVE Journal - Biology

Transfecting Human Neural Stem Cells with the Amaxa Nucleofector

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Cited by 10 •

2007

Introducing a gene of interest into a cell is a powerful method for elucidating its function in vivo. This protocol describes an efficient method of transfecting a culture of human neural stem/precursor cells (hNSPCs) using the Nucleofector electroporation apparatus made by Amaxa.

A Technique for Gene Editing in Natural Killer Cells Using CRISPR Cas9

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2025

This video demonstrates a technique for Cas9 ribonucleoprotein-mediated genetic modification of primary natural killer (NK) cells. A Cas9 ribonucleoprotein, consisting of a Cas9 endonuclease bound to a guide RNA (gRNA) formed by base pairing a CRISPR RNA (crRNA) and a trans-activating crRNA (tracrRNA), is introduced into primary natural killer cells via electroporation. The ribonucleoprotein targets and cleaves the host DNA at the target site, leading to gene knockout via modification of the...

Generation and Genetic Manipulation of Human Cervical Organoids

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2026

We present a detailed protocol to establish and genetically manipulate human cervical organoids.

Efficient Generation and Editing of Feeder-free IPSCs from Human Pancreatic Cells Using the CRISPR-Cas9 System

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Cited by 4 •

2017

This protocol describes in detail the generation of footprint-free induced pluripotent stem cells (iPSCs) from human pancreatic cells in feeder-free conditions, followed by editing using CRISPR/Cas9 ribonucleoproteins and characterization of the modified single-cell clones.

Education

JoVE Science Education - Advanced Biology

Neuronal Transfection Methods

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2023

Transfection - the process of transferring genetic material into cells - is a powerful tool for the rapid and efficient manipulation of gene expression in cells. Because this method can be used to silence the expression of specific proteins or to drive the expression of foreign or modified proteins, transfection is an extremely useful tool in the study of the cellular and molecular processes that govern neuron function. However, mature neurons have a number of properties that make them...

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