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SMPD3 Knockout Cell Lines

Gene: SMPD3

Official Full Name: sphingomyelin phosphodiesterase 3provided by HGNC

Gene Summary: Enables sphingomyelin phosphodiesterase activity. Involved in sphingomyelin catabolic process. Predicted to be located in plasma membrane. Predicted to be active in cytoplasm. Biomarker of pulmonary emphysema. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02689 SMPD3 Knockout cell line (HEK293) Human SMPD3 1:3~1:6 Negative Online Inquiry

Background

SMPD3 Gene Knockout Cell Lines are genetically engineered cell lines in which the SMPD3 gene, responsible for encoding sphingomyelin phosphodiesterase 3, has been deliberately disrupted or "knocked out". These cell lines serve as powerful tools for elucidating the role of SMPD3 in various biological processes, including sphingolipid metabolism, apoptosis, and cellular signaling pathways. The knockout mechanism typically utilizes CRISPR-Cas9 or similar gene-editing technologies, enabling precise modifications that facilitate the study of gene function and interaction.

The primary function of SMPD3 is related to the hydrolysis of sphingomyelin to ceramide, playing a pivotal role in regulating cellular responses to stress, inflammation, and apoptosis. By utilizing these knockout cell lines, researchers can investigate the downstream effects of SMPD3 loss-of-function mutations within various contexts, such as cancer progression and neurodegenerative diseases. The ability to observe cellular responses devoid of SMPD3 provides insights into its contribution to pathophysiological conditions, making these cell lines invaluable for both basic and applied research.

In clinical settings, SMPD3 Gene Knockout Cell Lines can enhance the development of gene therapies and pharmacological interventions targeting sphingolipid pathways. Furthermore, they allow for screening potential therapeutic compounds that modulate SMPD3 activity and can facilitate personalized medicine approaches for diseases linked with sphingolipid dysregulation.

What sets SMPD3 Gene Knockout Cell Lines apart from alternatives is their increased specificity and reliability in studying gene function without contamination from residual SMPD3 activity. Compared to traditional techniques, these knockout models offer high throughput and the capacity for comprehensive genetic analyses, allowing researchers to derive more precise conclusions and enhance reproducibility across experiments.

For researchers and clinicians committed to advancing their understanding of molecular mechanisms in disease and therapeutic targets, these knockout cell lines are invaluable. Our company specializes in the development and distribution of high-quality, customizable biological products, leveraging cutting-edge technologies and expertise in genetic engineering to support your research endeavors and clinical applications.

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

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