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NOTCH2 Knockout Cell Lines

Gene: NOTCH2

Official Full Name: notch receptor 2provided by HGNC

Gene Summary: This gene encodes a member of the Notch family. Members of this Type 1 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 family members play a role in a variety of developmental processes by controlling cell fate decisions. The Notch signaling network is an evolutionarily conserved intercellular signaling pathway which regulates interactions between physically adjacent cells. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signaling pathway that plays a key role in development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remain to be determined. This protein is cleaved in the trans-Golgi network, and presented on the cell surface as a heterodimer. This protein functions as a receptor for membrane bound ligands, and may play a role in vascular, renal and hepatic development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO11358 NOTCH2 Knockout cell line (HeLa) Human NOTCH2 1:3~1:6 Negative Online Inquiry
KO11359 NOTCH2 Knockout cell line (HCT 116) Human NOTCH2 1:2~1:4 Negative Online Inquiry
KO11360 NOTCH2 Knockout cell line (HEK293) Human NOTCH2 1:3~1:6 Negative Online Inquiry
KO11361 NOTCH2 Knockout cell line (A549) Human NOTCH2 1:3~1:4 Negative Online Inquiry

Background

NOTCH2 Gene Knockout Cell Lines are specifically engineered cellular models that allow researchers to elucidate the role of the NOTCH2 gene in various biological processes and diseases. The NOTCH signaling pathway is crucial for cell differentiation, proliferation, and apoptosis, and alterations in its components, such as NOTCH2, have been linked to a variety of cancer types, developmental disorders, and other diseases. The cell lines are created using advanced CRISPR/Cas9 gene editing techniques, ensuring precise knockout of the NOTCH2 gene, thereby facilitating detailed study of its functions and the resultant phenotypic changes.

These knockout cell lines serve a pivotal role in dissecting the mechanisms of NOTCH2 in developmental biology and oncogenesis. Researchers can examine alterations in cell signaling, gene expression, and cellular behaviors, providing critical insights into how misregulation of NOTCH2 contributes to pathological states. Additionally, the availability of these model systems fosters the development of novel therapeutic strategies targeting aberrant NOTCH signaling pathways in malignancies.

One of the notable advantages of our NOTCH2 Gene Knockout Cell Lines is their robustness and consistency in experimental outcomes, compared to traditional wild-type cells or less sophisticated knockout models. Unlike alternative systems that may lack specificity or introduce off-target effects, these engineered lines offer both high fidelity and reproducibility in research settings.

By utilizing our NOTCH2 Gene Knockout Cell Lines, researchers and clinicians can accelerate their understanding of NOTCH2-related pathophysiology, driving advances in targeted therapies and personalized medicine approaches. Our commitment to precision gene editing techniques and comprehensive support reflects our expertise in providing invaluable biological products that empower scientific discovery and innovation. With a deep understanding of molecular genetics and cell biology, our team is dedicated to fostering breakthroughs in research while ensuring that our clients have access to the highest-quality scientific tools.

Please note that all services are for research use only. Not intended for any clinical use.

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