Gene: IFT74
Official Full Name: intraflagellar transport 74provided by HGNC
Gene Summary: This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome. [provided by RefSeq, Mar 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO26166 | IFT74 Knockout cell line (HeLa) | Human | IFT74 | 1:3~1:6 | Negative | Online Inquiry |
KO26167 | IFT74 Knockout cell line (HCT 116) | Human | IFT74 | 1:2~1:4 | Negative | Online Inquiry |
KO26168 | IFT74 Knockout cell line (HEK293) | Human | IFT74 | 1:3~1:6 | Negative | Online Inquiry |
KO26169 | IFT74 Knockout cell line (A549) | Human | IFT74 | 1:3~1:4 | Negative | Online Inquiry |
IFT74 Gene Knockout Cell Lines are genetically engineered cell models designed to specifically disable the IFT74 gene, which plays a crucial role in the intraflagellar transport (IFT) pathway—vital for the assembly and maintenance of cilia and flagella. By utilizing CRISPR-Cas9 technology, these knockout cell lines allow researchers to study the loss-of-function effects associated with the IFT74 gene, providing insights into ciliary assembly and signaling processes.
The primary function of IFT74 involves facilitating the transport of protein complexes along the ciliary axoneme, essential for maintaining cilium structure and function. Disruption of this gene can lead to a variety of diseases, including ciliopathies, which are genetic disorders that result from dysfunctional cilia. By employing IFT74 knockout cell lines, scientists are equipped with a powerful tool to elucidate the downstream effects of IFT dysfunction, investigate associated phenotypic changes, and explore potential therapeutic avenues for targeting ciliary diseases.
In terms of scientific importance, these cell lines not only enhance our understanding of fundamental cellular mechanisms but also have wide-ranging applications in drug discovery, genetic research, and the investigation of developmental biology. The ability to mimic human disease conditions in vitro presents a significant advantage for translating research findings into clinical settings.
Compared to traditional methods of gene knockout, such as homologous recombination, IFT74 Gene Knockout Cell Lines offer a streamlined and efficient approach with higher specificity and reduced off-target effects. Additionally, these cell lines can be cultured and maintained under standard laboratory conditions, making them readily accessible for high-throughput screening applications.
For researchers and clinicians, the value of IFT74 Gene Knockout Cell Lines lies in their potential to accelerate discoveries related to ciliary function and dysfunction, ultimately contributing to novel therapeutic strategies for ciliopathy-related diseases. Our company has a proven track record in producing high-quality biological products tailored for cutting-edge research, ensuring that our customers have access to the best tools for scientific advancement.
Please note that all services are for research use only. Not intended for any clinical use.
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