Targeted Gene Delivery Using CRISPR/Cas9 Precision Editing at the Cellular Level
Received Date: Dec 02, 2024 / Published Date: Dec 30, 2024
Abstract
The advent of CRISPR/Cas9 technology has revolutionized the field of genetic engineering, enabling precision gene editing at the cellular level. This article explores the application of CRISPR/Cas9 in targeted gene delivery, focusing on its use in precise, efficient genetic modifications in both somatic cells and germline cells. CRISPR/Cas9 offers a transformative approach to correcting genetic defects, treating genetic diseases, and enhancing the understanding of gene function. The article covers the underlying mechanism of CRISPR/Cas9, its advantages over previous geneediting methods, current therapeutic applications, challenges in gene delivery, and potential risks. Moreover, we examine future developments and the ethical considerations surrounding the use of CRISPR/Cas9 in therapeutic settings. The goal of this review is to present an overview of the progress and potential of CRISPR/Cas9 in targeted gene delivery and its broader implications for personalized medicine.
Citation: Ziegler Z (2024) Targeted Gene Delivery Using CRISPR/Cas9 Precision Editing at the Cellular Level. J Anal Bioanal Tech 15: 707. Doi: 10.4172/2155-9910.1000707
Copyright: © 2024 Ziegler Z. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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