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ENG Knockout Cell Lines

Gene: ENG

Official Full Name: endoglinprovided by HGNC

Gene Summary: This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03207 ENG Knockout cell line (HeLa) Human ENG 1:3~1:6 Negative Online Inquiry
KO03208 ENG Knockout cell line (HCT 116) Human ENG 1:2~1:4 Negative Online Inquiry

Background

ENG Gene Knockout Cell Lines are meticulously engineered cellular models that feature specific gene knockouts targeting the endothelial nitric oxide synthase (eNOS) gene, a key regulator of nitric oxide (NO) production in vascular tissues. These cell lines serve as valuable tools for studying the effects of eNOS deficiency in physiological and pathological contexts, such as cardiovascular diseases and metabolic disorders. The knockout mechanism typically involves CRISPR-Cas9 technology, which allows for precise editing of the target gene, enabling researchers to observe both the absence of the gene and resultant phenotypic changes.

The primary function of these cell lines is to facilitate the exploration of endothelial function, vascular reactivity, and the underlying biological mechanisms that contribute to NO signaling pathways. By employing ENG Gene Knockout Cell Lines, scientists can effectively investigate the role of eNOS in various biological processes, consequently fostering advancements in therapeutic approaches that target related dysregulations.

In terms of scientific importance, these cell lines are essential in both basic research and translational studies, including drug discovery and development. Researchers can leverage these models to assess the impact of specific treatments on endothelial function without the interference of eNOS. This specificity is crucial for developing precision medicine interventions for cardiovascular-related health issues, thereby providing a clearer understanding of drug efficacy.

Compared to alternative models like wild-type cell lines, ENG Gene Knockout variants offer a significant advantage by allowing for the direct observation of phenotypic outcomes resulting from the loss of eNOS function, thus minimizing confounding variables. This specificity not only enhances the validity of experimental results but also accelerates the pace of discovery in cardiovascular research.

The ENG Gene Knockout Cell Lines represent a powerful asset for researchers and clinicians alike, providing insights that are instrumental in addressing the complex interplay between endothelial function and cardiovascular health. By harnessing the expertise and innovation of our company, which specializes in the development of high-quality biological products, we are proud to offer state-of-the-art tools that empower the scientific community to make significant strides in health research and clinical applications.

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

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