Gene: MTO1
Official Full Name: mitochondrial tRNA translation optimization 1provided by HGNC
Gene Summary: This gene encodes a mitochondrial protein thought to be involved in mitochondrial tRNA modification. The encoded protein may also play a role in the expression of the non-syndromic and aminoglycoside-induced deafness phenotypes associated with a specific mutation in the mitochondrial 12S rRNA gene. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28766 | MTO1 Knockout cell line (HeLa) | Human | MTO1 | 1:3~1:6 | Negative | Online Inquiry |
KO28767 | MTO1 Knockout cell line (HCT 116) | Human | MTO1 | 1:2~1:4 | Negative | Online Inquiry |
KO28768 | MTO1 Knockout cell line (HEK293) | Human | MTO1 | 1:3~1:6 | Negative | Online Inquiry |
KO28769 | MTO1 Knockout cell line (A549) | Human | MTO1 | 1:3~1:4 | Negative | Online Inquiry |
MTO1 Gene Knockout Cell Lines represent a significant advancement in the field of genetic research and therapeutic development, specifically designed to facilitate the study of mitochondrial tRNA modifications. These engineered cell lines feature targeted deletions of the MTO1 gene, which encodes a pivotal enzyme involved in the modification of mitochondrial tRNA, consequently affecting mitochondrial protein synthesis and cellular metabolism. By disrupting this gene, researchers can investigate the pivotal role of MTO1 in cellular function and its implications in various diseases, particularly those related to mitochondrial dysfunction.
The primary function of MTO1 Gene Knockout Cell Lines is to enable a deeper understanding of the cellular and molecular mechanisms underlying mitochondrial diseases. Through the use of these knockout models, scientists can analyze changes in mitochondrial morphology, respiratory function, and the overall dynamics of cellular metabolism. This is achieved by employing various assays, including mitochondrial respiration assessments and analyses of oxidative stress levels, thereby facilitating comprehensive studies into the consequences of impaired mitochondrial translation.
From a scientific perspective, these cell lines are invaluable for research and clinical applications alike. They provide an essential tool for elucidating the pathophysiological mechanisms of mitochondrial disorders and can aid in the development of targeted therapies. Researchers can utilize these cellular models to test new therapeutic interventions aimed at restoring mitochondrial function, ultimately contributing to improved treatment strategies for conditions such as mitochondrial myopathies and neurodegenerative diseases.
One distinct advantage of the MTO1 Gene Knockout Cell Lines over traditional cell models is their specificity and precision, allowing for a targeted examination of the effects of mitochondrial dysfunction without the confounding variables that often accompany non-knockout systems. Additionally, these cell lines are easy to culture and can be readily adapted for high-throughput screening applications, making them a versatile choice for laboratories focused on cutting-edge mitochondrial research.
The unique attributes of MTO1 Gene Knockout Cell Lines make them an essential resource for researchers and clinicians eager to unravel the complexities of mitochondrial biology and the therapeutic potential that lies within. Our company is dedicated to providing high-quality biological products that support the scientific community's endeavors in advancing knowledge and innovation in the field of genetics and molecular biology. Through our expertise and commitment to excellence, we strive to empower researchers with the tools they need to make significant breakthroughs in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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