Gene: TIMP2
Official Full Name: TIMP metallopeptidase inhibitor 2provided by HGNC
Gene Summary: This gene is a member of the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. In addition to an inhibitory role against metalloproteinases, the encoded protein has a unique role among TIMP family members in its ability to directly suppress the proliferation of endothelial cells. As a result, the encoded protein may be critical to the maintenance of tissue homeostasis by suppressing the proliferation of quiescent tissues in response to angiogenic factors, and by inhibiting protease activity in tissues undergoing remodelling of the extracellular matrix. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO34997 | TIMP2 Knockout cell line (HeLa) | Human | TIMP2 | 1:3~1:6 | Negative | Online Inquiry |
KO34998 | TIMP2 Knockout cell line (HCT 116) | Human | TIMP2 | 1:2~1:4 | Negative | Online Inquiry |
KO34999 | TIMP2 Knockout cell line (HEK293) | Human | TIMP2 | 1:3~1:6 | Negative | Online Inquiry |
KO35000 | TIMP2 Knockout cell line (A549) | Human | TIMP2 | 1:3~1:4 | Negative | Online Inquiry |
TIMP2 Gene Knockout Cell Lines are genetically engineered cellular models characterized by the targeted disruption of the TIMP2 (Tissue Inhibitor of Metalloproteinases 2) gene. This gene plays a critical role in regulating matrix metalloproteinases (MMPs), enzymes involved in the degradation of extracellular matrix components, influencing tissue remodeling and fibrotic processes. By providing a knockout of TIMP2, these cell lines allow researchers to elucidate the precise mechanisms of MMP regulation and the cellular responses associated with ECM dynamics.
The functionality of TIMP2 Gene Knockout Cell Lines is primarily rooted in their ability to facilitate the study of MMP activity in a controlled environment. By observing the effects of TIMP2 depletion, researchers can investigate the implications for cancer metastasis, wound healing, and cardiovascular diseases. The absence of TIMP2 enables a clearer understanding of pathological conditions associated with excessive ECM degradation, such as tumor invasion and progression, making this model invaluable for both basic and applied research.
Scientifically, these cell lines offer significant advantages in elucidating the complexities of cell signaling pathways influenced by TIMP2 activity. Compared to conventional cell lines where targeting gene function can be less specific or comprehensive, TIMP2 Gene Knockout Cell Lines provide a precise tool for studying gene function without the confounding effects of residual TIMP2 expression. This specificity enhances the reliability of experimental results and fosters a more accurate interpretation of data.
Researchers and clinicians will find TIMP2 Gene Knockout Cell Lines especially beneficial for developing novel therapeutic strategies aimed at MMP modulation. Their unique capabilities can help in designing targeted interventions to regulate ECM turnover in various disease contexts, thereby accelerating the translation of findings into clinical applications.
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