Gene: SLC25A42
Official Full Name: solute carrier family 25 member 42provided by HGNC
Gene Summary: This gene encodes a solute carrier family 25 protein. Solute carrier family 25 proteins are localized to mitochondria and play critical roles in the transport of molecules across the inner mitochondrial membrane. The encoded protein is a mitochondrial transporter for coenzyme A (CoA) and adenosine 3',5'-diphosphate. [provided by RefSeq, Feb 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05223 | SLC25A42 Knockout cell line (HeLa) | Human | SLC25A42 | 1:3~1:6 | Negative | Online Inquiry |
KO05224 | SLC25A42 Knockout cell line (HCT 116) | Human | SLC25A42 | 1:2~1:4 | Negative | Online Inquiry |
KO05225 | SLC25A42 Knockout cell line (HEK293) | Human | SLC25A42 | 1:3~1:6 | Negative | Online Inquiry |
SLC25A42 Gene Knockout Cell Lines are specialized cellular models engineered to lack the SLC25A42 gene, which encodes a mitochondrial transporter protein involved in metabolic processes. The depletion of this gene allows researchers to investigate the role of SLC25A42 in cellular physiology, energy metabolism, and mitochondrial function. These knockout cell lines serve as valuable tools for understanding disease mechanisms linked to mitochondrial dysfunction, particularly in conditions such as metabolic disorders, neurodegeneration, and cancer.
The primary function of SLC25A42 is to transport specific metabolites across the mitochondrial membrane, thereby influencing energy production and cellular respiration. By utilizing these knockout cell lines, scientists can assess the impact of absent SLC25A42 on cellular bioenergetics, redox state, and metabolite accumulation. The unique mechanism of action enables investigators to explore compensatory pathways activated in response to mitochondrial deficits, providing insights into potential therapeutic targets.
In the realm of research and clinical applications, SLC25A42 Gene Knockout Cell Lines are indispensable for elucidating the pathways involved in mitochondrial diseases and developing novel intervention strategies. These models facilitate high-throughput drug screening and gene editing approaches, enhancing their utility in functional genomics and personalized medicine.
Compared to alternative models, these knockout cell lines are derived from robust and well-characterized parental cell lines, ensuring consistent experimental reproducibility. They enable precise manipulation of mitochondrial function with minimal off-target effects, distinguishing them as reliable systems for detailed metabolic studies.
For researchers and clinicians focused on mitochondrial biology or therapeutic development, SLC25A42 Gene Knockout Cell Lines offer unparalleled insights that can drive innovation in treatment strategies. Our company specializes in developing cutting-edge biological products, ensuring that you have access to high-quality tools that advance scientific inquiry and contribute to meaningful breakthroughs in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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