Gene: ADAMTS17
Official Full Name: ADAM metallopeptidase with thrombospondin type 1 motif 17provided by HGNC
Gene Summary: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20001 | ADAMTS17 Knockout cell line (HCT 116) | Human | ADAMTS17 | 1:2~1:4 | Negative | Online Inquiry |
KO20002 | ADAMTS17 Knockout cell line (HEK293) | Human | ADAMTS17 | 1:3~1:6 | Negative | Online Inquiry |
ADAMTS17 Gene Knockout Cell Lines are genetically modified cell lines specifically engineered to lack the expression of the ADAMTS17 gene, which encodes a member of the ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin Motifs) family. This product allows researchers to investigate the various roles that ADAMTS17 plays in physiological and pathological processes, including extracellular matrix remodeling, angiogenesis, and cellular signaling pathways pertinent to diseases such as osteoarthritis and cancer.
The key function of these cell lines lies in their ability to facilitate insight into gene function through the study of phenotypic changes associated with the absence of ADAMTS17. By employing CRISPR-Cas9 technology for the gene knockout, these cell lines exhibit a definitive and reproducible loss of function, enabling detailed analysis of downstream effects on cell behavior, protein synthesis, and interaction with the extracellular matrix.
The scientific importance of ADAMTS17 Gene Knockout Cell Lines is underscored by their applications in both basic research and clinical settings. They serve as valuable tools for dissecting the molecular mechanisms of disease, screening potential therapeutic targets, and assessing drug efficacy in preclinical models. Researchers can leverage these cell lines to better understand the implications of ADAMTS17 in tissue homeostasis and disease progression.
Compared to alternative methods such as siRNA knockdown or overexpression systems, the ADAMTS17 knockout cell lines provide a stable and long-lasting model for studying gene function. This stability allows for repeated experiments and more meaningful data collection, which can be particularly beneficial in longitudinal studies.
For researchers and clinicians alike, the ability to directly model the effects of losing ADAMTS17 serves as a critical asset in advancing our understanding of various biological processes and developing targeted therapeutics. With a commitment to innovation and quality, our company prides itself on providing high-fidelity genetically modified cell lines, including the ADAMTS17 Gene Knockout Cell Lines, which are meticulously validated to ensure reliability and reproducibility in scientific research. Our expertise in cell line development positions us as a trusted partner in advancing your biological discovery goals.
Please note that all services are for research use only. Not intended for any clinical use.
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