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SCN8A Knockout Cell Lines

Gene: SCN8A

Official Full Name: sodium voltage-gated channel alpha subunit 8provided by HGNC

Gene Summary: This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with cognitive disability, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35498 SCN8A Knockout cell line (HCT 116) Human SCN8A 1:2~1:4 Negative Online Inquiry
KO35499 SCN8A Knockout cell line (HEK293) Human SCN8A 1:3~1:6 Negative Online Inquiry
KO35500 SCN8A Knockout cell line (A549) Human SCN8A 1:3~1:4 Negative Online Inquiry

Background

SCN8A Gene Knockout Cell Lines are genetically modified cellular models in which the SCN8A gene—encoding the voltage-gated sodium channel protein NaV1.6—has been inactivated. These cell lines serve as essential tools in the study of neuronal physiology and pathophysiology, particularly in understanding the implications of NaV1.6 dysfunction linked to various neurological disorders, including epilepsy and other ion channelopathies.

The central mechanism of SCN8A Gene Knockout Cell Lines lies in their ability to provide a controlled environment to investigate the role of SCN8A in action potential generation and neuronal excitability. When the SCN8A gene is knocked out, researchers can observe the resultant changes in cellular behavior, including altered ion flux, neurotransmitter release, and signal propagation. This makes these cell lines indispensable for studying disease mechanisms, pharmacological responses, and potential gene therapy approaches.

In clinical and research settings, the significance of these knockout models cannot be underestimated. They facilitate high-throughput screening for potential drug candidates, allowing scientists to evaluate the efficacy of pharmacological agents in targeting SCN8A-related pathways. Furthermore, these cell lines can be utilized to model patient-specific mutations, bridging the gap between genetic research and personalized medicine.

One of the key advantages of SCN8A Gene Knockout Cell Lines is their specificity and reproducibility. Unlike alternative models that may display a broad range of non-target effects, these cell lines offer precise insights into the SCN8A gene’s function, reducing experimental variability. This targeted approach enhances the reliability of experimental data, ensuring more consistent results that are crucial for rigorous scientific inquiry.

Researchers, clinicians, and pharmaceutical developers will find value in these cell lines for their unique ability to contribute to a deeper understanding of pathophysiological mechanisms and drug interactions. Investing in SCN8A Gene Knockout Cell Lines means gaining an invaluable asset for advancing neurological research and developing innovative therapeutic strategies.

At [Your Company Name], we pride ourselves on our commitment to providing high-quality, genetically engineered models that meet the rigorous standards of the scientific community, ensuring our researchers have access to the essential tools required for groundbreaking discoveries.

Please note that all services are for research use only. Not intended for any clinical use.

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