Gene: OXCT1
Official Full Name: 3-oxoacid CoA-transferase 1provided by HGNC
Gene Summary: This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00222 | OXCT1 Knockout cell line (HEK293) | Human | OXCT1 | 1:3~1:6 | Negative | Online Inquiry |
KO36251 | OXCT1 Knockout cell line (HeLa) | Human | OXCT1 | 1:3~1:6 | Negative | Online Inquiry |
KO36252 | OXCT1 Knockout cell line (HCT 116) | Human | OXCT1 | 1:2~1:4 | Negative | Online Inquiry |
KO36253 | OXCT1 Knockout cell line (A549) | Human | OXCT1 | 1:3~1:4 | Negative | Online Inquiry |
OXCT1 Gene Knockout Cell Lines are genetically engineered cell lines in which the OXCT1 gene has been specifically disrupted, allowing researchers to study the functional consequences of OXCT1 loss-of-function. This gene is responsible for encoding a protein involved in the metabolism of ketone bodies, specifically in the conversion of acetoacetate to acetoacetyl-CoA, a crucial step for energy production in various tissues, particularly during metabolic stress such as fasting or ketogenic diets. By utilizing these knockout cell lines, scientists can elucidate the biological mechanisms underlying metabolic disorders, neurological function, and energy homeostasis.
The key function of OXCT1 Gene Knockout Cell Lines lies in their ability to serve as a model for investigating the metabolic pathways that influence health and disease. The targeted disruption of OXCT1 provides a robust framework for studying the impact of impaired ketone body utilization on cellular metabolism, signaling pathways, and disease states, such as obesity, diabetes, and neurological disorders. These cell lines can be used to evaluate potential therapeutic targets and to assess the effects of pharmacological agents that aim to modulate metabolism.
The scientific importance of OXCT1 Gene Knockout Cell Lines extends into both research and clinical applications. They are invaluable in drug discovery programs aimed at developing innovative treatments for metabolic maladies. The use of these knockout models allows researchers to identify how altered energy metabolism can contribute to pathogenesis, ultimately leading to better-targeted therapies.
One significant advantage of OXCT1 Gene Knockout Cell Lines compared to alternative models is their specificity and precision in gene disruption, leading to translatable results in human cellular contexts. Additionally, these cell lines are meticulously validated for successful knockout efficiency, ensuring reproducibility and reliability in research findings.
In conclusion, OXCT1 Gene Knockout Cell Lines offer researchers and clinicians a powerful tool for advancing the understanding of metabolic regulation and its implications for health. By enabling detailed studies of metabolic pathways, these cell lines represent a crucial innovation in biological research. As a company dedicated to advancing scientific knowledge and providing high-quality research tools, we bring years of expertise in genetic engineering and cell line development, ensuring our products meet the rigorous demands of modern research.
Please note that all services are for research use only. Not intended for any clinical use.
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