Gene: IFT22
Official Full Name: intraflagellar transport 22provided by HGNC
Gene Summary: Predicted to enable GTPase activity. Predicted to be involved in intracellular protein transport. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06768 | IFT22 Knockout cell line (HeLa) | Human | IFT22 | 1:3~1:6 | Negative | Online Inquiry |
KO06769 | IFT22 Knockout cell line (HCT 116) | Human | IFT22 | 1:2~1:4 | Negative | Online Inquiry |
KO06770 | IFT22 Knockout cell line (HEK293) | Human | IFT22 | 1:3~1:6 | Negative | Online Inquiry |
KO06771 | IFT22 Knockout cell line (A549) | Human | IFT22 | 1:3~1:4 | Negative | Online Inquiry |
IFT22 Gene Knockout Cell Lines are meticulously engineered cellular models designed to study the functional implications of the IFT22 gene, which plays a critical role in the intraflagellar transport (IFT) process. This process is essential for the maintenance and functioning of cilia and flagella in eukaryotic cells. By creating knockout models of IFT22, researchers can effectively investigate the downstream consequences of its absence and gain insights into various cellular mechanisms, including those linked to developmental processes and disease states.
The key function of these knockout cell lines lies in their ability to elucidate the biology of cilia through the systematic analysis of morphological and functional changes that occur when IFT22 is disrupted. Mechanistically, the absence of IFT22 hampers the transport of essential cargo, leading to impaired ciliogenesis and subsequent dysfunctions that may manifest in various pathways, from signaling to cell communication. This makes the IFT22 knockout cell lines invaluable for studying conditions associated with defective cilia, such as ciliopathies and neurodegenerative diseases.
In scientific research and clinical applications, these cell lines represent pivotal tools for both basic and translational research. By allowing the identification of potential therapeutic targets and the screening of compounds that may rescue the ciliogenic defects induced by IFT22 knockout, researchers can advance their understanding of related pathologies. Furthermore, the ability to generate reproducible and consistent experimental models enhances the reliability of research findings, thereby accelerating the discovery process in both academic and clinical environments.
What sets IFT22 Gene Knockout Cell Lines apart from alternative models is their specificity and precision in manipulating the gene of interest, coupled with robust validation of knockout efficiency. These cell lines are constructed using cutting-edge CRISPR technology, ensuring minimal off-target effects and high fidelity in gene editing. As a result, they provide an unparalleled platform for detailed pathway analysis and drug discovery.
For researchers and clinicians aiming to deepen their understanding of cilia-related biology and its implications in human health, these knockout cell lines offer a unique and highly valuable resource. Our company, with extensive expertise in gene editing technologies and the development of sophisticated biological tools, is dedicated to delivering innovative solutions that empower advancements in life sciences and medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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