Gene: MGME1
Official Full Name: mitochondrial genome maintenance exonuclease 1provided by HGNC
Gene Summary: The protein encoded by this gene is a nuclear-encoded mitochondrial protein necessary for the maintenance of mitochondrial genome synthesis. The encoded protein is a RecB-type exonuclease and primarily cleaves single-stranded DNA. Defects in this gene have been associated with mitochondrial DNA depletion syndrome-11. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22735 | MGME1 Knockout cell line (HeLa) | Human | MGME1 | 1:3~1:6 | Negative | Online Inquiry |
KO22736 | MGME1 Knockout cell line (HCT 116) | Human | MGME1 | 1:2~1:4 | Negative | Online Inquiry |
KO22737 | MGME1 Knockout cell line (HEK293) | Human | MGME1 | 1:3~1:6 | Negative | Online Inquiry |
KO22738 | MGME1 Knockout cell line (A549) | Human | MGME1 | 1:3~1:4 | Negative | Online Inquiry |
MGME1 Gene Knockout Cell Lines are a specialized biological tool designed to facilitate the comprehensive study of the MGME1 gene, which encodes a key component involved in mitochondrial genome maintenance. These knockout cell lines are engineered to possess a complete inactivation of the MGME1 gene, enabling researchers to elucidate the functional roles and pathways associated with mitochondrial DNA repair, replication, and overall cellular metabolism. By removing the gene's expression, scientists can closely observe the physiological consequences and cellular responses, thereby advancing our understanding of mitochondrial biology.
The key mechanism by which these cell lines operate involves the disruption of normal mitochondrial DNA processing, which is essential for maintaining mitochondrial integrity. By utilizing CRISPR-Cas9 technology or other gene-editing strategies, these MGME1 knockout cell lines present a controlled environment to investigate the potential accumulation of mitochondrial DNA lesions, changes in oxidative stress responses, and alterations in cellular energy metabolism pathways.
In the realm of scientific research, these cell lines are particularly valuable in both basic research settings and clinical applications. They serve as indispensable models for studying mitochondrial diseases, aging, and metabolic disorders. Moreover, they provide insights that may lead to therapeutic targets for conditions resulting from mitochondrial dysfunction.
The specific advantages of MGME1 Gene Knockout Cell Lines lie in their precision and reliability compared to conventional knockout methods, which may exhibit partial or transient effects. These cell lines offer a stable genetic background, ensuring reproducibility in experiments and enhancing the quality of data generated. Furthermore, their versatility enables researchers across various disciplines, including molecular biology, genetics, and pharmacology, to explore a broad spectrum of mitochondrial-related research questions.
For researchers and clinicians focusing on mitochondrial health and disease, MGME1 Gene Knockout Cell Lines represent a unique and indispensable asset. They not only allow for rigorous investigation of gene function but also pave the way for the development of novel therapeutic strategies.
At our company, we pride ourselves on delivering high-quality biological products backed by extensive expertise in genetic engineering and cellular biology. Our commitment to advancing research through innovative solutions ensures that scientists and healthcare professionals have access to resources that support groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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