Gene: CC2D2B
Official Full Name: coiled-coil and C2 domain containing 2Bprovided by HGNC
Gene Summary: Predicted to be involved in non-motile cilium assembly and protein localization to ciliary transition zone. Predicted to be active in ciliary transition zone. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO19045 | CC2D2B Knockout cell line (HEK293) | Human | CC2D2B | 1:3~1:6 | Negative | Online Inquiry |
CC2D2B Gene Knockout Cell Lines represent a precise and functional biological tool designed to facilitate in-depth genetic research. These cell lines are engineered to specifically lack the CC2D2B gene, a crucial factor involved in cilia formation and signaling pathways, which has significant implications in various diseases, including ciliopathies. By providing a model that lacks this gene, researchers can explore the downstream effects of its absence, enabling a better understanding of its role in cellular processes and disease mechanisms.
The key function of the CC2D2B Gene Knockout Cell Lines lies in their ability to mimic a pathological state in a controlled environment. Utilizing advanced CRISPR-Cas9 gene-editing technology, these cell lines not only validate gene function but also facilitate the study of compensatory mechanisms and alternative pathways that may be activated in the absence of CC2D2B. This makes them vital for investigating the etiology of diseases related to ciliary dysfunction.
In terms of scientific importance, CC2D2B Gene Knockout Cell Lines are a crucial asset in both basic and translational research. They can be utilized in drug screening assays, genetic interaction studies, and therapeutic target validation, thereby advancing our understanding of ciliopathies at the genetic and molecular levels.
With their unique specificity and robust performance, these cell lines outperform traditional knockout models that may possess off-target effects or incomplete gene deletions. As a result, researchers and clinicians seeking reliable and reproducible results can significantly benefit from their use, driving innovation in genetic research and clinical applications.
Our company specializes in providing high-quality biological products designed to accelerate scientific discovery. With a commitment to excellence and precision in our offerings, we empower researchers to push the boundaries of genetic knowledge and therapeutic development.
Please note that all services are for research use only. Not intended for any clinical use.
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