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ADAMTS10 Knockout Cell Lines

Gene: ADAMTS10

Official Full Name: ADAM metallopeptidase with thrombospondin type 1 motif 10provided by HGNC

Gene Summary: This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO25656 ADAMTS10 Knockout cell line (HeLa) Human ADAMTS10 1:3~1:6 Negative Online Inquiry
KO25657 ADAMTS10 Knockout cell line (HCT 116) Human ADAMTS10 1:2~1:4 Negative Online Inquiry
KO25658 ADAMTS10 Knockout cell line (HEK293) Human ADAMTS10 1:3~1:6 Negative Online Inquiry
KO25659 ADAMTS10 Knockout cell line (A549) Human ADAMTS10 1:3~1:4 Negative Online Inquiry

Background

ADAMTS10 Gene Knockout Cell Lines are genetically engineered cellular models that have been specifically designed to lack the expression of the ADAMTS10 gene, which encodes for a disintegrin and metalloproteinase with thrombospondin motifs. This unique modification facilitates the in-depth study of the gene’s role in various biological processes, including extracellular matrix remodeling, cell migration, and tissue homeostasis. By creating a controlled environment where ADAMTS10 is disabled, these knockout cell lines enable researchers to unravel the gene's function in both physiological and pathological contexts.

The key mechanism of action revolves around the absence of ADAMTS10, allowing for the exploration of its downstream effects on signaling pathways and cellular behavior. By utilizing these cell lines, investigators can assess alterations in matrix composition, changes in cell adhesion properties, and the impact on protein interactions that are pivotal for understanding diseases such as osteoarthritis and certain types of cancer.

In terms of scientific importance, ADAMTS10 Gene Knockout Cell Lines are invaluable in research settings focused on elucidating the mechanisms of diseases linked to extracellular matrix dysregulation. They serve as a powerful tool for drug discovery and can aid in the identification of novel therapeutic targets. Clinically, understanding ADAMTS10's role may lead to the development of targeted therapies that could significantly improve patient outcomes in related diseases.

What distinguishes our ADAMTS10 Gene Knockout Cell Lines from alternatives is their precision and reliability. Each cell line undergoes rigorous testing to confirm the complete disruption of ADAMTS10, ensuring consistent results across experiments. This level of validation not only enhances the reproducibility of research findings but also increases confidence among users when deriving conclusions from experimental data.

The value of these cell lines lies in their capacity to drive innovation in research and therapeutic development, filling a critical gap in studies of the extracellular matrix. Our company specializes in high-quality, genetically modified cell lines, having established a reputation for excellence in the field. By choosing our ADAMTS10 Gene Knockout Cell Lines, researchers and clinicians gain access to cutting-edge tools that empower their investigations and advance understanding in a key area of molecular biology.

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

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