Gene: E2F4
Official Full Name: E2F transcription factor 4provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein binds to all three of the tumor suppressor proteins pRB, p107 and p130, but with higher affinity to the last two. It plays an important role in the suppression of proliferation-associated genes, and its gene mutation and increased expression may be associated with human cancer. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO11564 | E2F4 Knockout cell line (HeLa) | Human | E2F4 | 1:3~1:6 | Negative | Online Inquiry |
KO11565 | E2F4 Knockout cell line (HCT 116) | Human | E2F4 | 1:2~1:4 | Negative | Online Inquiry |
KO11566 | E2F4 Knockout cell line (HEK293) | Human | E2F4 | 1:3~1:6 | Negative | Online Inquiry |
KO11567 | E2F4 Knockout cell line (A549) | Human | E2F4 | 1:3~1:4 | Negative | Online Inquiry |
E2F4 Gene Knockout Cell Lines represent a significant advancement in the study of cell cycle regulation and gene transcription. These engineered cell lines are depleted of the E2F4 transcription factor, a key player in controlling the progression from the G1 to the S phase of the cell cycle and influencing various cellular processes such as proliferation and differentiation. By knocking out the E2F4 gene, researchers can dissect the molecular pathways influenced by this protein and examine the consequences of its absence, thus providing valuable insights into tumorigenesis and developmental biology.
The functionality of E2F4 Gene Knockout Cell Lines lies in their ability to serve as a model system for studying the perturbations in cell cycle dynamics and gene expression associated with E2F4 deficiency. This product enables researchers to perform targeted experiments that elucidate the roles of E2F4 in cellular signaling and its interactions with other cell cycle proteins. Moreover, the knockout model allows for the analysis of compensatory mechanisms that may emerge in response to the loss of E2F4, making it a critical tool for understanding cancer biology and other diseases linked to cell cycle dysregulation.
From a scientific perspective, these cell lines hold immense potential in both research and clinical settings. They can be employed in drug discovery, aiding in the identification of new therapeutics that can modulate cell cycle checkpoints. Their application extends to functional genomics studies and the development of gene therapies aimed at correcting the dysregulation seen in cancers driven by aberrant E2F4 activity.
What sets E2F4 Gene Knockout Cell Lines apart from alternatives is their precision and reproducibility. Each cell line is meticulously characterized, ensuring that researchers can trust the integrity and consistency of their results. Additionally, these lines enable seamless integration with various assays for assessing cellular response to pharmacological agents, enhancing their value in preclinical research.
For researchers and clinicians looking to advance their work on cell cycle regulation and cancer, E2F4 Gene Knockout Cell Lines offer an invaluable resource. Our commitment to high-quality biological products ensures that you receive cutting-edge tools designed by experts in the field, empowering your research objectives and contributing to the broader landscape of biomedical discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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