Gene: NOTCH1
Official Full Name: notch receptor 1provided by HGNC
Gene Summary: This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01396 | NOTCH1 Knockout cell line (HeLa) | Human | NOTCH1 | 1:3~1:6 | Negative | Online Inquiry |
KO11362 | NOTCH1 Knockout cell line (HCT 116) | Human | NOTCH1 | 1:2~1:4 | Negative | Online Inquiry |
KO11363 | NOTCH1 Knockout cell line (HEK293) | Human | NOTCH1 | 1:3~1:6 | Negative | Online Inquiry |
KO11364 | NOTCH1 Knockout cell line (A549) | Human | NOTCH1 | 1:3~1:4 | Negative | Online Inquiry |
NOTCH1 Gene Knockout Cell Lines are meticulously engineered cellular models designed to study the Notch signaling pathway, a critical regulator of cell fate determination, differentiation, and proliferation. Through targeted gene editing techniques, such as CRISPR-Cas9, these cell lines have been generated to specifically knock out the NOTCH1 gene, facilitating researchers in the exploration of its functional roles and the implications of its dysregulation in various oncological and developmental contexts.
The NOTCH1 protein plays a pivotal role in mediating communication between adjacent cells, influencing processes such as stem cell maintenance and immune responses. By utilizing these knockout cell lines, researchers can observe resultant phenotypic changes and dissect the downstream effects of NOTCH1 signaling disruption. This enables in-depth exploration of tumorigenesis mechanisms, particularly in hematological malignancies, where aberrant NOTCH1 activity is often implicated.
From a scientific perspective, the applications of NOTCH1 Gene Knockout Cell Lines are invaluable in both basic and applied research. They serve as powerful tools for investigating drug development, therapeutic targets, and biomarker identification, ultimately contributing to more effective treatment modalities for patients. Moreover, their implications extend into gene therapy and regenerative medicine, where understanding Notch's role is crucial for developing innovative strategies.
Compared to other methodologies, these knockout cell lines offer precise gene ablation with the ability to maintain native cellular context. This specificity enhances experimental reproducibility and accuracy over broad-spectrum inhibitors or RNA interference technologies, which may yield off-target effects and non-specific outcomes.
For researchers and clinicians, the value of NOTCH1 Gene Knockout Cell Lines lies in their ability to provide clear insights into Notch-mediated effects, potentially leading to breakthrough therapies tailored to individual patient needs. By employing these models, users can advance the frontiers of biomedical research and clinical interventions.
As a leader in the field of biological product development, our company harnesses advanced genetic engineering technologies to produce high-fidelity cellular models, ensuring researchers have access to the most innovative tools to push the boundaries of science.
Please note that all services are for research use only. Not intended for any clinical use.
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