Gene: IFT172
Official Full Name: intraflagellar transport 172provided by HGNC
Gene Summary: This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28238 | IFT172 Knockout cell line (HeLa) | Human | IFT172 | 1:3~1:6 | Negative | Online Inquiry |
KO28239 | IFT172 Knockout cell line (HCT 116) | Human | IFT172 | 1:2~1:4 | Negative | Online Inquiry |
KO28240 | IFT172 Knockout cell line (HEK293) | Human | IFT172 | 1:3~1:6 | Negative | Online Inquiry |
KO28241 | IFT172 Knockout cell line (A549) | Human | IFT172 | 1:3~1:4 | Negative | Online Inquiry |
IFT172 Gene Knockout Cell Lines are genetically modified cell lines that have been engineered to lack the expression of the IFT172 gene, which is critical for intraflagellar transport (IFT) processes in cilia and flagella. These cell lines serve as essential tools for investigating the physiological and molecular roles of IFT172 in cellular functions and disease mechanisms, particularly in studies related to ciliary dysfunction.
The primary function of these knockout cell lines is to elucidate the pathways and processes that involve ciliary assembly, maintenance, and signaling. IFT172 plays a pivotal role in transporting proteins along the ciliary axoneme, which is crucial for maintaining cellular homeostasis and signaling. By studying these knockout lines, researchers can gain insights into the dysregulation of ciliary functions associated with various conditions, such as Bardet-Biedl syndrome and Polycystic Kidney Disease.
In research and clinical settings, IFT172 Gene Knockout Cell Lines are invaluable for model systems enabling the identification of downstream effects of IFT172 absence. They allow for the exploration of compensatory mechanisms employed by cells in response to altered ciliary dynamics, promoting a deeper understanding of related pathologies. The scientific importance of this product is underscored by its ability to facilitate drug screening and the examination of therapeutic targets for the treatment of ciliary-related disorders.
Compared to traditional wild-type cell lines, IFT172 knockout models provide a clear advantage by giving direct insights into IFT-related dysfunctions without the confounding interference of normal gene expression. This precision aids in reducing experimental variability and enhances reproducibility for downstream applications.
For researchers and clinicians focused on developmental biology, genetic disorders, or ciliary function, the value of IFT172 Gene Knockout Cell Lines lies in their versatility and ability to serve as a targeted research platform. Their use can lead to significant breakthroughs in understanding disease mechanisms, paving the way for novel therapeutic strategies.
Our company, recognized for its commitment to advancing genetic research, brings extensive expertise in developing reliable and innovative genetic tools. With IFT172 knockout cell lines, we provide researchers with state-of-the-art products designed to aid in transformative scientific discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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