Gene: SPTLC3
Official Full Name: serine palmitoyltransferase long chain base subunit 3provided by HGNC
Gene Summary: This gene encodes a subunit of the serine palmitoyltransferase complex which catalyzes the rate-limiting step in sphingolipid biosynthesis. This subunit metabolizes lauroyl- and myristoyl-CoA and generates C14 and C16-sphingoid bases. [provided by RefSeq, Mar 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07682 | SPTLC3 Knockout cell line (HeLa) | Human | SPTLC3 | 1:3~1:6 | Negative | Online Inquiry |
SPTLC3 gene knockout cell lines are genetically engineered cell models designed to lack the functionality of the serine palmitoyltransferase, long chain base subunit 3 (SPTLC3) gene. This gene plays a critical role in the de novo synthesis of sphingolipids, which are vital components of cellular membranes and signaling molecules. By utilizing these knockout cell lines, researchers are able to investigate the biological and pathological roles of sphingolipid metabolism, particularly concerning neurodegenerative diseases, cancer, and metabolic disorders.
The primary mechanism of action in SPTLC3 knockout cell lines revolves around the disruption of sphingolipid biosynthesis, allowing scientists to elucidate the effects of altered sphingolipid levels on cellular function and signal transduction pathways. Inhibiting SPTLC3 expression leads to a distinctive phenotype that can be studied to provide insights into the consequences of disrupted lipid homeostasis and its subsequent impact on cellular health and function.
The scientific importance of these cell lines is underscored by their potential applications in both research and clinical settings. They serve as valuable tools in drug discovery, allowing for the screening of potential therapeutics that might target sphingolipid-related pathways. Additionally, in clinical research, these knockout models help to identify new biomarkers and therapeutic targets for conditions stemming from abnormal sphingolipid metabolism.
One of the distinct advantages of using SPTLC3 gene knockout cell lines is their specificity. Unlike general inhibitors that may affect multiple pathways, these genetically modified cells provide a refined system for studying the direct effects of SPTLC3 loss, thereby minimizing off-target effects and facilitating reproducibility in experiments. This specificity enhances the validity of the results, making it easier for researchers to draw meaningful conclusions from their studies.
For researchers and clinicians engaged in lipid biology, neurobiology, and cancer research, SPTLC3 gene knockout cell lines represent an invaluable resource. They are essential for unraveling complex biological processes and could potentially lead to groundbreaking discoveries in therapeutic interventions.
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