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IFT88 Knockout Cell Lines

Gene: IFT88

Official Full Name: intraflagellar transport 88provided by HGNC

Gene Summary: This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34316 IFT88 Knockout cell line (HeLa) Human IFT88 1:3~1:6 Negative Online Inquiry
KO34317 IFT88 Knockout cell line (HCT 116) Human IFT88 1:2~1:4 Negative Online Inquiry
KO34318 IFT88 Knockout cell line (HEK293) Human IFT88 1:3~1:6 Negative Online Inquiry
KO34319 IFT88 Knockout cell line (A549) Human IFT88 1:3~1:4 Negative Online Inquiry

Background

IFT88 Gene Knockout Cell Lines are highly specialized biological tools engineered to lack the intraflagellar transport protein 88 (IFT88), a crucial component of cilia and flagella assembly. These cell lines facilitate the investigation of ciliary function, signaling pathways, and related cellular processes by creating a model that mimics the conditions of diseases associated with cilia dysfunction, such as polycystic kidney disease and certain forms of retinal degeneration.

The primary mechanism underlying the function of IFT88 Gene Knockout Cell Lines revolves around their ability to decouple ciliary biogenesis from normal cellular operations. By lacking IFT88, these cells present a distinct phenotype that allows researchers to study the roles of cilia in signaling pathways, cellular motility, and development. This is particularly relevant in dissecting the molecular basis of ciliopathies, wherein aberrations in ciliogenesis lead to various human diseases.

The scientific importance of IFT88 Gene Knockout Cell Lines extends to both fundamental research and clinical applications. They provide a powerful model for exploring gene function, testing therapeutic interventions, and elucidating molecular mechanisms of disease in a controlled environment. This versatility makes them invaluable in drug discovery and development, especially regarding cilia-targeted therapeutics.

What sets IFT88 Gene Knockout Cell Lines apart from existing alternatives is their specific knockout feature, which ensures a reliable and reproducible model that accurately reflects the phenotypic characteristics associated with IFT88 loss. Furthermore, their ease of use and compatibility with a range of assays enhance their utility in high-throughput screening and functional genomics studies.

For researchers and clinicians focused on understanding and treating ciliopathies, the IFT88 Gene Knockout Cell Lines represent a significant advancement—enabling the exploration of intricate ciliary functions with precision. Our company prides itself on its commitment to providing cutting-edge research tools, underscored by a team of experts dedicated to advancing biological sciences. Our products, including the IFT88 Gene Knockout Cell Lines, are designed to empower scientists in their quest to uncover the complexities of cellular biology.

Please note that all services are for research use only. Not intended for any clinical use.

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