Gene: IFT52
Official Full Name: intraflagellar transport 52provided by HGNC
Gene Summary: This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO23057 | IFT52 Knockout cell line (HeLa) | Human | IFT52 | 1:3~1:6 | Negative | Online Inquiry |
KO23058 | IFT52 Knockout cell line (HCT 116) | Human | IFT52 | 1:2~1:4 | Negative | Online Inquiry |
KO23059 | IFT52 Knockout cell line (HEK293) | Human | IFT52 | 1:3~1:6 | Negative | Online Inquiry |
KO23060 | IFT52 Knockout cell line (A549) | Human | IFT52 | 1:3~1:4 | Negative | Online Inquiry |
IFT52 Gene Knockout Cell Lines are specialized cell lines that have undergone targeted gene disruption to knock out the IFT52 gene, which plays a crucial role in the intraflagellar transport (IFT) system. This system is essential for the assembly and maintenance of cilia and flagella, making it pivotal in various cellular processes such as signaling pathways and cell motility. By utilizing CRISPR-Cas9 genetic engineering techniques, IFT52 Gene Knockout Cell Lines provide researchers with invaluable tools to study the consequences of IFT dysfunction, further advancing our understanding of ciliopathies and related disorders.
The primary function of these knockout cell lines is to delineate the intricate mechanisms of ciliary function and transport, facilitating the examination of how the absence of IFT52 impacts cellular signaling, development, and homeostasis. Given the vital role of cilia in numerous biological processes, these knockout models can be employed in various applications, ranging from fundamental research to drug discovery efforts, particularly in studies investigating diseases such as polycystic kidney disease, Bardet-Biedl syndrome, and cancer.
One of the significant advantages of using IFT52 Gene Knockout Cell Lines is their specificity and precision, eliminating off-target effects often observed in less refined models. This specificity not only enhances the reliability of experimental outcomes but is also crucial for generating reproducible data that can lead to impactful scientific conclusions. Compared to traditional knockout methods, these cell lines provide more robust tools for dissecting signaling pathways and elucidating gene function through controlled experimental conditions.
Researchers, clinicians, and biotechnologists will find these cell lines particularly valuable for their ability to mimic human pathological conditions tied to IFT dysfunction, enhancing translational research efforts. Furthermore, the accessibility of these models enables a broader scope of experimentation, allowing teams to accelerate their research timelines.
With a strong commitment to advancing bioscience, our company specializes in providing high-quality biological products that empower the scientific community. Our expertise in gene editing technologies and cell line development ensures that our offerings are not only innovative but also rigorously validated, making them essential resources for advancing both basic and applied research.
Please note that all services are for research use only. Not intended for any clinical use.
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