Gene: MMP1
Official Full Name: matrix metallopeptidase 1provided by HGNC
Gene Summary: This gene encodes a member of the peptidase M10 family 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. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down the interstitial collagens, including types I, II, and III. The gene is part of a cluster of MMP genes on chromosome 11. Mutations in this gene are associated with chronic obstructive pulmonary disease (COPD). Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO09913 | MMP1 Knockout cell line (HeLa) | Human | MMP1 | 1:3~1:6 | Negative | Online Inquiry |
KO09914 | MMP1 Knockout cell line (HEK293) | Human | MMP1 | 1:3~1:6 | Negative | Online Inquiry |
MMP1 Gene Knockout Cell Lines are specially engineered cell lines in which the gene encoding Matrix Metalloproteinase 1 (MMP1) has been inactivated, providing a powerful tool for studying the role of this enzyme in various pathophysiological processes. MMP1 is a key player in extracellular matrix remodeling, wound healing, and tissue repair, as well as in the progression of diseases such as cancer and arthritis. By understanding MMP1’s functions through these knockout models, researchers can dissect molecular pathways and identify potential therapeutic targets.
The primary mechanism of action involves the complete ablation of MMP1 expression, which subsequently alters the behavior of cells in critical assays including migration, invasion, and secretory profiles. The absence of MMP1 allows for the investigation of compensatory mechanisms by other metalloproteinases or signaling pathways, thereby providing insights into cellular responses under pathological conditions. Additionally, the cell lines can be effectively utilized to screen for therapeutic compounds and evaluate their modulatory effects on tissue remodeling and disease progression.
The significance of MMP1 Gene Knockout Cell Lines extends into both research and clinical domains, particularly in studies involving tumor microenvironments, joint diseases, and fibrotic conditions. Their ability to mimic specific roles of MMP1 allows researchers and clinicians to model disease states accurately, advancing our understanding of mechanisms underlying disease and treatment outcomes.
Unique advantages of these cell lines include their reproducibility, specificity, and the capability to distinguish MMP1-related pathways from broader metalloproteinase activity, setting them apart from alternative models that may not offer this level of precision. Furthermore, these cell lines are invaluable for investigating gene-gene interactions and establishing a causal relationship in various experimental paradigms.
The value of MMP1 Gene Knockout Cell Lines lies in their ability to generate reliable and relevant data, which can significantly impact the development of novel therapies and diagnostic markers for diseases related to MMP1 dysregulation.
Our company has deep expertise in developing cutting-edge biological products, ensuring that researchers and clinicians have access to highly specialized tools that enhance their study designs and contribute to groundbreaking discoveries in the field of biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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