Gene: SCN5A
Official Full Name: sodium voltage-gated channel alpha subunit 5provided by HGNC
Gene Summary: The protein encoded by this gene is an integral membrane protein and tetrodotoxin-resistant voltage-gated sodium channel subunit. This protein is found primarily in cardiac muscle and is responsible for the initial upstroke of the action potential in an electrocardiogram. Defects in this gene have been associated with long QT syndrome type 3 (LQT3), atrial fibrillation, cardiomyopathy, and Brugada syndrome 1, all autosomal dominant cardiac diseases. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, May 2022]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35496 | SCN5A Knockout cell line (HCT 116) | Human | SCN5A | 1:2~1:4 | Negative | Online Inquiry |
KO35497 | SCN5A Knockout cell line (HEK293) | Human | SCN5A | 1:3~1:6 | Negative | Online Inquiry |
SCN5A Gene Knockout Cell Lines represent a groundbreaking tool in cardiovascular research, specifically designed to study the function and regulatory mechanisms of the SCN5A gene, which encodes the alpha subunit of the cardiac sodium channel NaV1.5. These cell lines, created through targeted gene editing techniques, allow researchers to investigate the effects of SCN5A loss-of-function mutations on cardiac excitability, arrhythmias, and related heart diseases. By eliminating the SCN5A gene, these models mimic the pathophysiological conditions associated with various cardiac disorders, providing critical insights into their molecular underpinnings.
The underlying mechanism of these knockout cell lines involves CRISPR-Cas9 technology, allowing for precise editing of the genome to inactivate the SCN5A gene. This targeted approach enables scientists to observe the resulting phenotypic changes, including alterations in action potential characteristics, ion channel activity, and signaling pathways essential for cardiac function. Such insights are pivotal for developing novel therapeutic strategies aimed at treating inherited arrhythmias and other cardiac dysfunctions.
The scientific importance of SCN5A Gene Knockout Cell Lines lies in their application across various research and clinical settings. They serve as an invaluable platform for drug screening, therapeutic exploration, and the elucidation of disease mechanisms. By utilizing these models, researchers can gain a deeper understanding of the physiological role of SCN5A and its implications in cardiovascular health.
Compared to traditional models, such as non-specific cell lines or in-vivo animal studies, SCN5A Gene Knockout Cell Lines offer superior specificity and control over the experimental conditions. They provide a more precise representation of human pathophysiology, significantly enhancing the potential for translational research and the development of targeted therapies.
For researchers and clinicians focused on cardiovascular health, integrating SCN5A Gene Knockout Cell Lines into their studies presents a transformative opportunity for advancing knowledge and therapeutic options. Our commitment to excellence in the development of high-quality biological products ensures that you are equipped with reliable tools to accelerate your research and clinical outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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