Gene: CCDC40
Official Full Name: coiled-coil domain 40 molecular ruler complex subunitprovided by HGNC
Gene Summary: This gene encodes a protein that is necessary for motile cilia function. It functions in correct left-right axis formation by regulating the assembly of the inner dynein arm and the dynein regulatory complexes, which control ciliary beat. Mutations in this gene cause ciliary dyskinesia type 15, a disorder due to defects in cilia motility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02968 | CCDC40 Knockout cell line (HeLa) | Human | CCDC40 | 1:3~1:6 | Negative | Online Inquiry |
KO02969 | CCDC40 Knockout cell line (HCT 116) | Human | CCDC40 | 1:2~1:4 | Negative | Online Inquiry |
KO02970 | CCDC40 Knockout cell line (HEK293) | Human | CCDC40 | 1:3~1:6 | Negative | Online Inquiry |
KO02971 | CCDC40 Knockout cell line (A549) | Human | CCDC40 | 1:3~1:4 | Negative | Online Inquiry |
CCDC40 Gene Knockout Cell Lines are genetically modified cell lines designed to investigate the functional roles of the CCDC40 gene, which encodes a protein implicated in ciliary structure and function. These knockout cell lines are generated using precise genome-editing techniques, such as CRISPR-Cas9, rendering the CCDC40 gene inactive and allowing researchers to study the resultant cellular phenotypes. By providing a model to analyze the absence of this specific gene, scientists can gain insights into its contributions to cellular mechanisms, including motility, signal transduction, and developmental biology.
The primary function of CCDC40 is linked to the assembly and maintenance of cilia, which are crucial organelles involved in various signaling pathways and sensory functions. The absence of CCDC40 in these knockout cell lines enables researchers to discern the implications of impaired ciliary function on cellular behavior, contribute to the understanding of ciliopathies, and investigate potential therapeutic avenues for associated disorders.
The scientific importance of CCDC40 Gene Knockout Cell Lines is underscored by their application in both fundamental research and clinical settings. They serve as powerful tools for studying diseases related to ciliary dysfunction, such as respiratory illnesses and certain genetic syndromes. They are invaluable in developing targeted therapies and understanding disease mechanisms, significantly advancing the field of cell biology and genetics.
In comparison to alternative models, such as wild-type or overexpressing cell lines, CCDC40 knockout models provide a direct and specific approach to understand loss-of-function scenarios that may not be achievable through traditional genetic models. Their precision enables highly reproducible results that can lead to innovative findings and applications.
For researchers and clinicians examining ciliary-related diseases, the CCDC40 Gene Knockout Cell Lines represent a crucial resource that can catalyze discoveries in the pathogenesis of various ciliopathies. Our company is dedicated to delivering advanced genetic tools, and our expertise in cell line development ensures that our products meet the highest standards of quality and performance, empowering advancements in biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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