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NOTCH3 Knockout Cell Lines

Gene: NOTCH3

Official Full Name: notch receptor 3provided by HGNC

Gene Summary: This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00212 NOTCH3 gRNA1-gRNA2 KO plasmid NOTCH3 $850
KO00641 NOTCH3 Knockout cell line(Huh-7) Human NOTCH3 1:2~1:3 Negative Online Inquiry
KO11354 NOTCH3 Knockout cell line (HeLa) Human NOTCH3 1:3~1:6 Negative Online Inquiry
KO11355 NOTCH3 Knockout cell line (HCT 116) Human NOTCH3 1:2~1:4 Negative Online Inquiry
KO11356 NOTCH3 Knockout cell line (HEK293) Human NOTCH3 1:3~1:6 Negative Online Inquiry
KO11357 NOTCH3 Knockout cell line (A549) Human NOTCH3 1:3~1:4 Negative Online Inquiry

Background

NOTCH3 Gene Knockout Cell Lines are sophisticated biological tools designed to facilitate the study of the NOTCH3 gene, integral to cellular signaling pathways involved in various developmental processes and disease states, particularly in neurodegeneration and cardiovascular conditions. These customized cell lines are generated through advanced gene-editing technologies, such as CRISPR/Cas9, that effectively disrupt the NOTCH3 gene expression, allowing researchers to investigate the functional consequences of its absence.

The primary function of NOTCH3 gene knockout cell lines is to elucidate the role of NOTCH signaling in cellular mechanisms, such as proliferation, differentiation, and apoptosis. By providing a controlled experimental system, these cell lines enable researchers to dissect the pathways influenced by NOTCH3, examining its involvement in diseases like CADASIL syndrome—a hereditary condition that affects blood flow to the brain and is linked to NOTCH3 mutations—alongside other pathological manifestations.

In research and clinical settings, the applications of NOTCH3 knockout cell lines extend beyond fundamental biology; they are invaluable in drug discovery and development, potentially accelerating the identification of therapeutic targets for various conditions. Their utility is further accentuated by enabling high-throughput screening for small molecules that might correct aberrant NOTCH signaling.

Compared to other gene editing models, the NOTCH3 knockout cell lines stand out for their specificity and reliability, allowing for reproducible results without the confounding variables associated with other methods of gene silencing. This specificity is crucial for generating data that are clear and interpretable, ultimately leading to innovative solutions in healthcare and therapeutic strategies.

For researchers and clinicians aiming to deepen their understanding of NOTCH3’s role in health and disease, these knockout cell lines present a unique opportunity to contribute to the body of knowledge that could drive scientific advancements. Our company leverages years of expertise in genetic engineering and cell line development, ensuring that our products meet the highest standards of quality and efficacy, thereby supporting the quest for scientific progress in understanding complex biological systems.

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

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