Gene: ACVRL1
Official Full Name: activin A receptor like type 1provided by HGNC
Gene Summary: This gene encodes a type I cell-surface receptor for the TGF-beta superfamily of ligands. It shares with other type I receptors a high degree of similarity in serine-threonine kinase subdomains, a glycine- and serine-rich region (called the GS domain) preceding the kinase domain, and a short C-terminal tail. The encoded protein, sometimes termed ALK1, shares similar domain structures with other closely related ALK or activin receptor-like kinase proteins that form a subfamily of receptor serine/threonine kinases. Mutations in this gene are associated with hemorrhagic telangiectasia type 2, also known as Rendu-Osler-Weber syndrome 2. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO09880 | ACVRL1 Knockout cell line (HEK293) | Human | ACVRL1 | 1:3~1:6 | Negative | Online Inquiry |
ACVRL1 Gene Knockout Cell Lines are specifically engineered cellular models that allow for the precise study of the Activin A receptor-like kinase 1 (ALK1), a key component involved in vascular biology and several pathophysiological processes. These cell lines are invaluable tools for researchers looking to understand the molecular mechanisms underlying vascular development and associated disorders such as hereditary hemorrhagic telangiectasia (HHT) and other angiogenic diseases. By knocking out the ACVRL1 gene, researchers can dissect the pathways activated by its absence, revealing crucial insights into angiogenesis and vascular remodeling.
The primary function of ACVRL1 Gene Knockout Cell Lines lies in their ability to model the loss-of-function scenarios that researchers often encounter in clinical settings. The knockout of the ACVRL1 gene alters signaling pathways mediated by bone morphogenetic proteins (BMPs), leading to altered cellular responses such as differentiation, proliferation, and apoptosis. This model facilitates a deeper understanding of how dysregulation in these pathways can lead to diseases. Moreover, these cell lines can be utilized for high-throughput drug screening and the assessment of therapeutic compounds aimed at targeting ALK1 signaling.
From a scientific perspective, the use of ACVRL1 Gene Knockout Cell Lines can significantly advance the understanding of vascular pathologies and help validate potential therapeutic targets in research and clinical settings. Unlike traditional models, these specialized knockout lines provide a clearer interpretation of results, making the data more reproducible and relevant for translational research.
Compared to traditional wild-type cell lines, ACVRL1 Gene Knockout Cell Lines afford researchers a robust and specific resource for studying the implications of ALK1 loss and its role in vascular malformations. They are easy to culture and can be utilized across various experimental setups, ensuring versatile application in both fundamental and applied life sciences.
In conclusion, our commitment to advancing biological research is reflected in the development of ACVRL1 Gene Knockout Cell Lines. Our expertise in gene editing technologies and cell culture systems provides researchers and clinicians with the tools necessary to unravel complex biological questions and drive innovative solutions in vascular biology.
Please note that all services are for research use only. Not intended for any clinical use.
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