Crispr Gene Tagging

CRISPR gene tagging is a genome-editing technique that adds a detectable sequence, such as a fluorescent protein or epitope tag, to a chosen gene so its expression or protein behavior can be studied in living cells. A guide RNA directs Cas9 to a matching DNA sequence, where the nuclease creates a targeted break; a repair template can then insert the tag through homology-directed repair while preserving the gene’s regulatory context. In neuroscience, endogenous tagging helps researchers track neuronal proteins, visualize their location and movement, and measure changes during development, synaptic signaling, or disease. This approach supports more precise studies of brain-cell function than methods relying only on overexpressed reporter constructs.

Crispr Gene Tagging - Related Videos

Research

JoVE Journal - Biology

CRISPR/Cas9-mediated Endogenous Fluorescent Tagging of Germline-specific Genes in Caenorhabditis elegans

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2026

A CRISPR/Cas9 microinjection workflow for endogenous fluorescent tagging in the Caenorhabditis elegans germline to obtain homozygous knock-in lines for in vivo protein localization analysis.

One-step CRISPR-based Strategy for Endogenous Gene Tagging in Drosophila melanogaster

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Cited by 2 •

2024

Here, we present a simplified endogenous gene tagging protocol for Drosophila, which utilizes a PCR-based technique for marker-free identification of successful genetic modifications, facilitating the development of stable knock-in lines.

Research

JoVE Journal - Immunology and Infection
Free Sample

High-throughput Gene Tagging in Trypanosoma brucei

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Cited by 21 •

2016

Addition of a tag to a protein is a powerful way of gaining insight into its function. Here, we describe a protocol to endogenously tag hundreds of Trypanosoma brucei proteins in parallel such that genome scale tagging is achievable.

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...

Education

JoVE Core - Biology

CRISPR

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2019

Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced Short...

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