Gene: FOXJ3
Official Full Name: forkhead box J3provided by HGNC
Gene Summary: Enables DNA-binding transcription activator activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO30201 | FOXJ3 Knockout cell line (HeLa) | Human | FOXJ3 | 1:3~1:6 | Negative | Online Inquiry |
KO30202 | FOXJ3 Knockout cell line (HCT 116) | Human | FOXJ3 | 1:2~1:4 | Negative | Online Inquiry |
KO30203 | FOXJ3 Knockout cell line (HEK293) | Human | FOXJ3 | 1:3~1:6 | Negative | Online Inquiry |
KO30204 | FOXJ3 Knockout cell line (A549) | Human | FOXJ3 | 1:3~1:4 | Negative | Online Inquiry |
FOXJ3 Gene Knockout Cell Lines are specialized cellular models created to facilitate the comprehensive study of the FOXJ3 gene, an essential transcription factor involved in the regulation of ciliary development and function. The process of gene knockout involves the targeted disruption or deletion of the FOXJ3 gene, effectively rendering these cell lines incapable of producing functional FOXJ3 protein. This disruption allows researchers to investigate the gene's specific roles in cellular processes such as motility, signaling pathways, and organ development, contributing to a deeper understanding of cilia-associated diseases.
The key functions of FOXJ3 Gene Knockout Cell Lines stem from their inability to produce the FOXJ3 protein, yielding distinct phenotypic changes that can be systematically studied. Researchers can utilize these cell lines to explore the implications of FOXJ3 deficiency on ciliogenesis, cellular adhesion, and response to external stimuli. The mechanistic insights gleaned from these investigations are crucial for elucidating the pathophysiology of conditions such as primary ciliary dyskinesia (PCD) and other cilia-related disorders.
The scientific importance of FOXJ3 Gene Knockout Cell Lines extends to various research and clinical applications, including drug development, disease modeling, and gene therapy research. By providing a robust platform for exploring genetic functions and potential therapeutic interventions, these cell lines are invaluable for movement towards precision medicine and targeted therapies.
What sets FOXJ3 Gene Knockout Cell Lines apart from alternative models is their specificity and reliability, derived from rigorous validation processes that ensure consistent and reproducible results. They are easily manipulated and compatible with various high-throughput screening methods, enhancing their usability in diverse experimental setups.
For researchers and clinicians interested in the nuances of ciliary biology and associated diseases, these cell lines offer an unparalleled opportunity to drive forward scientific discovery and clinical advancements. Our company specializes in the development and production of genetically modified cell lines, ensuring that each product is of the highest quality, backed by our extensive expertise in molecular biology and genetic engineering. Through our commitment to innovation and excellence, we empower scientists to unlock the complexities of gene function to address pressing health challenges.
Please note that all services are for research use only. Not intended for any clinical use.
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