Gene: MTMR7
Official Full Name: myotubularin related protein 7provided by HGNC
Gene Summary: This gene encodes a member of the myotubularin family of tyrosine/dual-specificity phosphatases. The encoded protein is characterized by four distinct domains that are conserved among all members of the myotubularin family: the glucosyltransferase, Rab-like GTPase activator and myotubularins domain, the Rac-induced recruitment domain, the protein tyrosine phosphatases and dual-specificity phosphatases domain and the suppressor of variegation 3-9, enhancer-of-zeste, and trithorax interaction domain. This protein dephosphorylates the target substrates phosphatidylinositol 3-phosphate and inositol 1,3-bisphosphate. A pseudogene of this gene is found on chromosome 5. [provided by RefSeq, Mar 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07859 | MTMR7 Knockout cell line (HeLa) | Human | MTMR7 | 1:3~1:6 | Negative | Online Inquiry |
KO07860 | MTMR7 Knockout cell line (HCT 116) | Human | MTMR7 | 1:2~1:4 | Negative | Online Inquiry |
KO07861 | MTMR7 Knockout cell line (HEK293) | Human | MTMR7 | 1:3~1:6 | Negative | Online Inquiry |
KO07862 | MTMR7 Knockout cell line (A549) | Human | MTMR7 | 1:3~1:4 | Negative | Online Inquiry |
MTMR7 Gene Knockout Cell Lines are specialized cellular models engineered to lack the MTMR7 gene, which encodes for the protein myotubularin-related protein 7. These cell lines serve as vital tools for studying the functional implications of MTMR7 in cellular processes such as autophagy, membrane traffic, and phosphoinositide metabolism. The knockout of the MTMR7 gene allows researchers to elucidate the role of this protein in various biological pathways, providing insight into its contributions to diseases, particularly those related to muscle degeneration and metabolic dysfunctions.
The key function of the MTMR7 gene knockout involves the disruption of normal signaling pathways that are critical for cellular homeostasis. This is achieved through mechanisms such as altered lipid metabolism and impact on protein phosphorylation, allowing scientists to explore the gene’s involvement in conditions like Charcot-Marie-Tooth disease and other myopathies. By utilizing these cell lines, researchers can conduct detailed investigations into the physiological roles of MTMR7, making them indispensable in gene-function studies and drug discovery efforts.
The scientific importance of MTMR7 gene knockout cell lines is underscored by their ability to provide insights into the molecular underpinnings of diseases associated with MTMR7 dysregulation. In research settings, they can serve as in vitro platforms for drug testing and development, paving the way for new therapeutic strategies targeting related pathologies. Clinically, these cell lines offer potential for advancing personalized medicine approaches by allowing better understanding of patient-specific mutations.
Compared to alternative models, MTMR7 gene knockout cell lines provide a more precise and controlled environment for studying the gene's effects, eliminating confounding variables that can arise in non-targeted systems. This specificity enhances the reliability and reproducibility of experimental results, making them a preferred choice for rigorous scientific research.
For researchers and clinicians, the availability of MTMR7 gene knockout cell lines represents an invaluable asset in advancing our understanding of molecular biology and the development of innovative therapeutic solutions. Our company specializes in providing high-quality biological products and expertise that empower scientific discovery and translational research, ensuring researchers have access to the optimal tools necessary for their studies.
Please note that all services are for research use only. Not intended for any clinical use.
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