Gene: IFT57
Official Full Name: intraflagellar transport 57provided by HGNC
Gene Summary: Predicted to enable DNA binding activity. Acts upstream of or within apoptotic process; positive regulation of cysteine-type endopeptidase activity; and regulation of apoptotic process. Located in ciliary base and photoreceptor connecting cilium. Part of intraciliary transport particle B. Implicated in orofaciodigital syndrome XVIII. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO17002 | IFT57 Knockout cell line (HeLa) | Human | IFT57 | 1:3~1:6 | Negative | Online Inquiry |
KO17003 | IFT57 Knockout cell line (HCT 116) | Human | IFT57 | 1:2~1:4 | Negative | Online Inquiry |
KO17004 | IFT57 Knockout cell line (HEK293) | Human | IFT57 | 1:3~1:6 | Negative | Online Inquiry |
KO17005 | IFT57 Knockout cell line (A549) | Human | IFT57 | 1:3~1:4 | Negative | Online Inquiry |
IFT57 Gene Knockout Cell Lines are genetically modified cells designed to lack functional IFT57 genes, which play a crucial role in the intraflagellar transport (IFT) pathway essential for ciliogenesis and various cellular signaling processes. These cell lines provide researchers with valuable tools for studying the impact of IFT57 deficiency on cellular functions, including cilia formation, cell signaling, and the associated pathophysiological conditions that arise from ciliary dysfunction.
The primary mechanism underlying the utility of IFT57 Gene Knockout Cell Lines lies in their ability to mimic disease states linked to aberrant ciliogenesis. By observing morphological and functional changes in these knockout cell lines, scientists can elucidate the downstream effects of IFT57 loss on signaling pathways such as Hedgehog, Notch, and Wnt. Furthermore, these cell lines facilitate high-throughput screening for potential therapeutic compounds that may restore proper ciliogenesis or mitigate dysfunction-related pathways.
The scientific relevance of IFT57 Gene Knockout Cell Lines extends across various research domains, including developmental biology, cancer research, and genetic disorders associated with cilia. Their application in both in vitro studies and therapeutic discovery makes them a cornerstone resource for elucidating the complexities of ciliary diseases.
In comparison to existing alternatives, IFT57 Gene Knockout Cell Lines offer a distinct advantage in their precise genetic modification and reproducibility, allowing for robust experimental designs. This specificity enhances the reliability of results obtained, making the learning curve less steep for researchers new to genetic manipulation techniques.
For researchers and clinicians focused on understanding the mechanisms behind ciliary function and dysfunction, these cell lines represent an invaluable resource. They allow for a deeper understanding of cilia-related diseases and contribute significantly to the discovery of novel therapeutic strategies.
Our company prides itself on its rigorous scientific standards and innovative approach to developing advanced biological products. With a team of experts dedicated to quality and accuracy, we ensure that our offerings, including the IFT57 Gene Knockout Cell Lines, support and enhance your research initiatives.
Please note that all services are for research use only. Not intended for any clinical use.
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