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SLC25A46 Knockout Cell Lines

Gene: SLC25A46

Official Full Name: solute carrier family 25 member 46provided by HGNC

Gene Summary: This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO23533 SLC25A46 Knockout cell line (HeLa) Human SLC25A46 1:3~1:6 Negative Online Inquiry
KO23534 SLC25A46 Knockout cell line (HCT 116) Human SLC25A46 1:2~1:4 Negative Online Inquiry
KO23535 SLC25A46 Knockout cell line (HEK293) Human SLC25A46 1:3~1:6 Negative Online Inquiry
KO23536 SLC25A46 Knockout cell line (A549) Human SLC25A46 1:3~1:4 Negative Online Inquiry

Background

SLC25A46 Gene Knockout Cell Lines are genetically engineered cell lines designed specifically to facilitate the investigation of the SLC25A46 gene's function within cellular processes. The SLC25A46 gene encodes a mitochondrial inner membrane protein that plays a critical role in mitochondrial dynamics, including bioenergetics, fusion, and fission. These knockout cell lines enable researchers to study the absence of the SLC25A46 gene and its associated phenotypes, shedding light on its contribution to mitochondrial disorders and cellular metabolism.

The primary function of SLC25A46 is related to the transport of metabolites across the mitochondrial membrane, a process essential for maintaining metabolic homeostasis. By utilizing CRISPR/Cas9 and other gene-editing technologies, our SLC25A46 knockout cell lines exhibit a complete ablation of the gene’s expression, allowing researchers to effectively dissect the downstream molecular pathways and cellular responses triggered by the lack of SLC25A46.

In the realm of scientific research and clinical applications, the SLC25A46 knockout cell lines serve as pivotal tools for elucidating the pathophysiology of various mitochondrial diseases, which have significant implications for understanding neurodegenerative disorders and metabolic syndromes. These cell lines facilitate high-throughput screening for potential therapeutic agents and can aid in the development of targeted treatments aimed at repairing mitochondrial dysfunction.

Compared to alternative models, such as wild-type cell lines or whole animal models, our SLC25A46 knockout cell lines offer several distinct advantages, including increased experimental control, reproducibility, and the ability to perform detailed mechanistic studies. Researchers benefit from a more streamlined approach to genetic studies and drug screening, ultimately enhancing the translational potential of their findings.

For researchers and clinicians focused on mitochondrial research, our SLC25A46 Gene Knockout Cell Lines provide a valuable, reliable resource that accelerates discovery and innovation in this critical area of health. Our company is dedicated to advancing scientific knowledge through high-quality biological products, backed by extensive expertise in genetic engineering and cell biology, empowering researchers to unlock new pathways and improve patient outcomes.

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

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