Gene: FOXRED2
Official Full Name: FAD dependent oxidoreductase domain containing 2provided by HGNC
Gene Summary: Enables flavin adenine dinucleotide binding activity. Involved in ERAD pathway. Located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO26295 | FOXRED2 Knockout cell line (HeLa) | Human | FOXRED2 | 1:3~1:6 | Negative | Online Inquiry |
KO26296 | FOXRED2 Knockout cell line (HCT 116) | Human | FOXRED2 | 1:2~1:4 | Negative | Online Inquiry |
KO26297 | FOXRED2 Knockout cell line (HEK293) | Human | FOXRED2 | 1:3~1:6 | Negative | Online Inquiry |
KO26298 | FOXRED2 Knockout cell line (A549) | Human | FOXRED2 | 1:3~1:4 | Negative | Online Inquiry |
FOXRED2 Gene Knockout Cell Lines are specifically engineered cell lines in which the FOXRED2 gene has been inactivated using advanced CRISPR-Cas9 technology. FOXRED2 is a critical gene associated with various cellular processes, including mitochondrial function, metabolism, and regulation of cellular stress responses. By knocking out this gene, researchers can investigate the underlying mechanisms of related diseases and explore potential therapeutic targets.
The key function of these cell lines lies in their ability to mimic pathological conditions by disrupting the normal action of the FOXRED2 gene. This provides a robust platform for studying mitochondrial dysfunction and its implications in diseases such as cancer, neurodegeneration, and metabolic disorders. The knockout cell lines offer a variety of experimental advantages, including controlled environments for genetic and pharmacological assessments, allowing for the elucidation of gene function and the testing of novel therapeutic agents.
From a scientific standpoint, the FOXRED2 Gene Knockout Cell Lines are invaluable for both academic and clinical research settings. They facilitate investigations into mitochondrial biology and the role of FOXRED2 in cellular signaling pathways, contributing to a deeper understanding of various diseases. Moreover, these models can be used in high-throughput screening assays, making them essential tools for drug discovery and validation.
Compared with traditional cell line models, the FOXRED2 knockout variants offer specificity and precision in studying gene function. While conventional methods may involve random mutagenesis or siRNA knockdown—methods that can lead to variable results—our knockout technology ensures a reliable, reproducible loss-of-function phenotype. This specificity is paramount for researchers seeking consistent and interpretable results.
With their unique capabilities, FOXRED2 Gene Knockout Cell Lines represent a powerful resource for scientists, enabling them to push the boundaries of research in mitochondrial-related diseases. Our company's expertise in gene editing and cell line development ensures that you receive high-quality products tailored to meet the needs of cutting-edge research. We are committed to supporting groundbreaking discoveries and enhancing the potential for therapeutic advancements in biological science.
Please note that all services are for research use only. Not intended for any clinical use.
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