Gene: SFXN2
Official Full Name: sideroflexin 2provided by HGNC
Gene Summary: Predicted to enable transmembrane transporter activity. Involved in mitochondrial transmembrane transport. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03452 | SFXN2 Knockout cell line (HeLa) | Human | SFXN2 | 1:3~1:6 | Negative | Online Inquiry |
KO03453 | SFXN2 Knockout cell line (HCT 116) | Human | SFXN2 | 1:2~1:4 | Negative | Online Inquiry |
KO03454 | SFXN2 Knockout cell line (HEK293) | Human | SFXN2 | 1:3~1:6 | Negative | Online Inquiry |
KO03455 | SFXN2 Knockout cell line (A549) | Human | SFXN2 | 1:3~1:4 | Negative | Online Inquiry |
SFXN2 Gene Knockout Cell Lines are specialized cellular models engineered to disrupt the SFXN2 gene, which encodes for a protein involved in various mitochondrial functions and iron-sulfur cluster biogenesis. These cell lines serve as a vital resource for investigating the biological role of SFXN2, particularly in cellular metabolism, oxidative stress response, and mitochondrial health.
The key function of SFXN2 gene knockout cell lines is to allow for the comprehensive study of the physiological and pathological consequences of SFXN2 absence. By employing CRISPR-Cas9 or similar gene-editing technologies, these cell lines enable researchers to dissect the gene's function at the molecular level, examining alterations in metabolic pathways and cellular signaling mechanisms. This can help in exploring conditions such as neurodegenerative diseases, metabolic syndromes, and various cancers, where mitochondrial dysfunction plays a critical role.
From a scientific standpoint, the study of SFXN2 knockouts is paramount for understanding iron metabolism and its implications in human diseases. These cell lines can facilitate drug discovery by providing a platform for screening potential therapeutic compounds that target mitochondrial dysfunctions or iron regulation pathways, extending their applications into translational research.
Compared to alternative genetic models, SFXN2 gene knockout cell lines offer unique advantages such as precise gene editing, reproducibility, and the ability to monitor real-time changes in cellular behavior in response to various stimuli. This specificity not only enhances experimental accuracy but also reduces variability often seen in traditional knockout models.
Researchers and clinicians value these cell lines as essential tools for advancing knowledge in mitochondrial biology, bridging gaps in our understanding of disease mechanisms, and informing potential therapeutic interventions. The precise and controlled genetic modifications provided by SFXN2 knockout models empower scientists to push the boundaries of current biological research.
Our company specializes in delivering cutting-edge biological research tools, with a focus on providing reliable and advanced products that meet the stringent needs of researchers worldwide. With our expertise and commitment to quality, we strive to support advancements in science and healthcare through innovative solutions like the SFXN2 Gene Knockout Cell Lines.
Please note that all services are for research use only. Not intended for any clinical use.
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