Gene: MRM3
Official Full Name: mitochondrial rRNA methyltransferase 3provided by HGNC
Gene Summary: Efficient translation of mitochondrial-derived transcripts requires proper assembly of the large subunit of the mitochondrial ribosome. Central to the biogenesis of this large subunit is the A-loop of mitochondrial 16S rRNA, which is modified by three rRNA methyltransferases located near mtDNA nucleoids. The protein encoded by this gene methylates G(1370) of 16S rRNA, and this modification is necessary for proper ribosomal large subnit assembly. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20912 | MRM3 Knockout cell line (HeLa) | Human | MRM3 | 1:3~1:6 | Negative | Online Inquiry |
KO20913 | MRM3 Knockout cell line (HCT 116) | Human | MRM3 | 1:2~1:4 | Negative | Online Inquiry |
KO20914 | MRM3 Knockout cell line (HEK293) | Human | MRM3 | 1:3~1:6 | Negative | Online Inquiry |
KO20915 | MRM3 Knockout cell line (A549) | Human | MRM3 | 1:3~1:4 | Negative | Online Inquiry |
MRM3 Gene Knockout Cell Lines are meticulously engineered cellular models where the MRM3 gene, responsible for mitochondrial ribosome biogenesis, has been functionally inactivated. These knockout lines are created through advanced genome-editing techniques such as CRISPR-Cas9, ensuring precise deletion of the gene's coding sequence. The resultant cell lines provide researchers with a robust platform to investigate the implications of MRM3 deficiency on mitochondrial function, cellular metabolism, and broader physiological processes.
The primary function of MRM3 involves the assembly of mitochondrial ribosomal RNA, which is critical for protein synthesis within the mitochondria. By studying these knockout cell lines, researchers can elucidate the mechanism by which MRM3 influences mitochondrial translation and how its dysfunction may contribute to mitochondrial diseases or metabolic disorders. This makes MRM3 knockout cell lines an invaluable tool in both basic research and translational studies aimed at understanding mitochondrial dynamics and their impact on human health.
The scientific importance of these cell lines is underscored by their applications in drug discovery, genetics, and disease modeling. They allow for the exploration of therapeutic strategies aimed at correcting mitochondrial deficiencies, thereby paving the way for innovative treatments. Furthermore, the unique advantage of MRM3 Gene Knockout Cell Lines lies in their specificity; unlike other models that may induce off-target effects, these cell lines provide a precise means to study the direct consequences of MRM3 ablation.
For researchers and clinicians, the value of these cell lines extends beyond basic functionality— they represent a significant advancement in understanding complex biological systems. Their use can lead to breakthroughs in targeted therapies, especially for diseases rooted in mitochondrial dysfunction. With our extensive expertise in cellular engineering and genetic modeling, we take pride in offering MRM3 Gene Knockout Cell Lines as a reliable resource that enhances scientific investigation and propels research forward.
Please note that all services are for research use only. Not intended for any clinical use.
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