Gene: CUL7
Official Full Name: cullin 7provided by HGNC
Gene Summary: The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05626 | CUL7 Knockout cell line (HeLa) | Human | CUL7 | 1:3~1:6 | Negative | Online Inquiry |
KO05627 | CUL7 Knockout cell line (HCT 116) | Human | CUL7 | 1:2~1:4 | Negative | Online Inquiry |
KO05628 | CUL7 Knockout cell line (HEK293) | Human | CUL7 | 1:3~1:6 | Negative | Online Inquiry |
KO05629 | CUL7 Knockout cell line (A549) | Human | CUL7 | 1:3~1:4 | Negative | Online Inquiry |
CUL7 Gene Knockout Cell Lines are specifically engineered cellular models that lack the CUL7 gene, a participant in the ubiquitin-proteasome system essential for protein degradation and cell cycle regulation. These knockout cell lines are crucial for studying the functional role of CUL7 in various biological processes, including cell proliferation, differentiation, and apoptosis. Through the use of CRISPR-Cas9 or similar gene-editing technologies, researchers can investigate the downstream effects of CUL7 absence, enabling a better understanding of diseases such as tumorigenesis and metabolic disorders.
The primary mechanism of CUL7 is its involvement in E3 ubiquitin ligase complexes, which facilitate the selective degradation of target proteins. By studying the CUL7 knockout cell lines, researchers can explore how the dysregulation of this pathway leads to aberrant cell behavior, providing valuable insights into cancer biology and potential therapeutic targets. Moreover, these cell lines serve as a practical tool for drug screening, allowing scientists to assess the effectiveness of novel compounds in a controlled environment.
The scientific importance of CUL7 Gene Knockout Cell Lines extends to both fundamental and applied research settings, making them indispensable for advancing our understanding of cellular mechanisms and therapeutic interventions. Compared to alternatives, such as transient knockdowns or overexpression systems, stable knockout cell lines offer a more consistent and reproducible model, enabling longitudinal studies and high-throughput screening.
For researchers and clinicians, the value of these cell lines lies in their ability to provide a clear phenotype linked to CUL7 deficiency, thereby enhancing the understanding of complex diseases. The precision and reliability of CUL7 knockout cell lines in experimental setups are unparalleled, ensuring robust and interpretable results, which are essential for the advancement of scientific knowledge.
Our company specializes in delivering quality biological products, including meticulously validated knockout cell lines. With a commitment to driving research advancements, we leverage our extensive expertise in molecular biology and genetic engineering to support the scientific community’s pursuit of groundbreaking discoveries and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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