Gene: IFT81
Official Full Name: intraflagellar transport 81provided by HGNC
Gene Summary: The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO27264 | IFT81 Knockout cell line (HeLa) | Human | IFT81 | 1:3~1:6 | Negative | Online Inquiry |
KO27265 | IFT81 Knockout cell line (HCT 116) | Human | IFT81 | 1:2~1:4 | Negative | Online Inquiry |
KO27266 | IFT81 Knockout cell line (HEK293) | Human | IFT81 | 1:3~1:6 | Negative | Online Inquiry |
KO27267 | IFT81 Knockout cell line (A549) | Human | IFT81 | 1:3~1:4 | Negative | Online Inquiry |
IFT81 Gene Knockout Cell Lines are specialized cell lines engineered to exhibit a complete deletion of the IFT81 gene, which encodes a protein essential for intraflagellar transport (IFT), a critical process in the assembly and maintenance of cilia. These cell lines serve as indispensable tools for researchers investigating the molecular mechanisms of cilia-related diseases, as IFT is crucial for the transportation of proteins and signaling molecules along ciliary axonemes.
The primary function of the IFT81 gene knockout cell lines is to facilitate the study of the downstream effects of IFT disruption. By eliminating the IFT81 protein, researchers can observe alterations in ciliary dynamics, cellular signaling pathways, and overall cell physiology. This unique mechanism allows scientists to delineate the roles of IFT in diverse biological processes, including development, sensory perception, and pathogenesis of ciliopathies such as Bardet-Biedl Syndrome and Polycystic Kidney Disease.
From a scientific perspective, the utility of IFT81 knockout cell lines extends to both fundamental research and clinical applications. They enable high-throughput screening of potential therapeutic compounds targeting ciliary dysfunction and provide a model for understanding how defects in IFT contribute to disease phenotypes. This model is particularly valuable for drug developers and genetic researchers aiming to unravel complex cellular pathways.
The advantages of using our IFT81 gene knockout cell lines include their high fidelity in mimicking physiological conditions, rigorous quality control measures, and the comprehensive characterization of the cell lines provided, ensuring reproducibility and reliability in research outcomes. Unlike traditional cell models, this offering allows for targeted investigations into low-abundance proteins and their specific roles in disease mechanisms.
In summary, IFT81 Gene Knockout Cell Lines present an unparalleled opportunity for researchers and clinicians seeking to advance their knowledge of ciliary biology and its implications in health and disease. With a commitment to scientific excellence, our company specializes in providing high-quality biological tools that facilitate groundbreaking research and innovation in the life sciences.
Please note that all services are for research use only. Not intended for any clinical use.
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