Gene: MMP17
Official Full Name: matrix metallopeptidase 17provided by HGNC
Gene Summary: This gene encodes a member of the peptidase M10 family and membrane-type subfamily of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Members of this subfamily contain a transmembrane domain suggesting that these proteins are expressed at the cell surface rather than secreted. The encoded preproprotein is proteolytically processed to generate the mature protease. This protein is unique among the membrane-type matrix metalloproteinases in that it is anchored to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor. Elevated expression of the encoded protein has been observed in osteoarthritis and multiple human cancers. [provided by RefSeq, Jan 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36591 | MMP17 Knockout cell line (HeLa) | Human | MMP17 | 1:3~1:6 | Negative | Online Inquiry |
KO36592 | MMP17 Knockout cell line (HCT 116) | Human | MMP17 | 1:2~1:4 | Negative | Online Inquiry |
KO36593 | MMP17 Knockout cell line (HEK293) | Human | MMP17 | 1:3~1:6 | Negative | Online Inquiry |
KO36594 | MMP17 Knockout cell line (A549) | Human | MMP17 | 1:3~1:4 | Negative | Online Inquiry |
MMP17 Gene Knockout Cell Lines are specialized cellular models engineered to specifically disrupt the expression of the matrix metalloproteinase 17 (MMP17) gene. MMP17, also known as membrane-type matrix metalloproteinase (MT-MMP), plays a pivotal role in extracellular matrix (ECM) remodeling and is implicated in various physiological and pathological processes, including tissue repair, cancer progression, and inflammatory responses. By utilizing these knockout cell lines, researchers can engage in in-depth studies of MMP17's function in cellular processes and its involvement in disease mechanisms without the confounding effects of gene expression.
The key mechanism by which these knockout cell lines operate is through targeted gene editing technologies—such as CRISPR/Cas9 or RNA interference—allowing for specific, efficient elimination of MMP17 activity. This targeted approach facilitates precise functional studies on how the absence of MMP17 influences cellular behavior, ECM interactions, and signal transduction pathways.
The scientific importance of MMP17 Gene Knockout Cell Lines cannot be overstated. They allow researchers to delineate the role of this protease in tumorigenesis, invasive behavior of cancer cells, and other pathologies where ECM dynamics are crucial. This makes them invaluable for drug development, biomarker identification, and the understanding of disease progression in both basic research and translational medicine.
Compared to traditional cell lines lacking specificity in gene knockout or modest reductions in gene expression, MMP17 Gene Knockout Cell Lines offer a definitive alternative that results in complete loss-of-function. This specificity ensures more reliable experimental outcomes and enhances the reproducibility of study results, providing researchers with a clearer understanding of MMP17's contributions to cellular physiology and disease.
For researchers and clinicians aiming to unlock the complexities of ECM regulation and its implications in health and disease, these knockout cell lines represent a potent tool. The ability to investigate the nuances of MMP17 activity opens new avenues for therapeutic strategies targeting ECM-related disorders.
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Please note that all services are for research use only. Not intended for any clinical use.
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