Gene: MRPL50
Official Full Name: mitochondrial ribosomal protein L50provided by HGNC
Gene Summary: Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a putative 39S subunit protein and belongs to the L47P ribosomal protein family. Pseudogenes corresponding to this gene are found on chromosomes 2p, 2q, 5p, and 10q. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO04589 | MRPL50 Knockout cell line (HeLa) | Human | MRPL50 | 1:3~1:6 | Negative | Online Inquiry |
KO04590 | MRPL50 Knockout cell line (HCT 116) | Human | MRPL50 | 1:2~1:4 | Negative | Online Inquiry |
KO04591 | MRPL50 Knockout cell line (HEK293) | Human | MRPL50 | 1:3~1:6 | Negative | Online Inquiry |
KO04592 | MRPL50 Knockout cell line (A549) | Human | MRPL50 | 1:3~1:4 | Negative | Online Inquiry |
MRPL50 Gene Knockout Cell Lines are specially engineered cell lines that possess a targeted ablation of the mitochondrial ribosomal protein L50 (MRPL50) gene. This gene is integral to mitochondrial ribosome function and protein synthesis, and its knockout allows researchers to elucidate the crucial role that mitochondrial protein synthesis plays in cellular metabolism, energy production, and apoptosis. The effective deletion of MRPL50 can be achieved through CRISPR/Cas9 technology, providing a precise tool for studying gene function and the downstream effects of mitochondrial dysfunction.
The key function of these knockout cell lines lies in their ability to mimic mitochondrial diseases and metabolic disorders, thereby serving as invaluable models in research settings. By exploring the consequences of MRPL50 depletion, scientists can investigate the differential pathways activated during mitochondrial stress, identify potential therapeutic targets, and evaluate the efficacy of pharmacological interventions. These cell lines are particularly useful in the study of various diseases, including cancer and neurodegenerative disorders where mitochondrial dysfunction is a pivotal factor.
One significant advantage of MRPL50 Gene Knockout Cell Lines is their high specificity and reproducibility, offering researchers consistent models to work with over extended periods. Unlike traditional models that may carry multiple genetic variations, these knockout lines provide a clean slate for studying the effects of MRPL50 absence, resulting in more accurate interpretations of experimental outcomes.
In addition, the MRPL50 knockout model presents unique selling points compared to other cellular models. Unlike general knockouts that can lead to compensatory mechanisms, the specific targeting of MRPL50 ensures that researchers obtain insights into the unique role of this ribosomal protein without the confounding effects of other genetic backgrounds. This specificity is critical in the context of drug discovery and functional genomics.
For researchers, clinicians, and biotech companies, the MRPL50 Gene Knockout Cell Lines represent a sophisticated tool that can drive the understanding of mitochondrial roles in health and disease. They facilitate the discovery of novel therapeutic strategies, ensuring that researchers have access to innovative resources that enhance their investigations.
With a commitment to excellence in biotechnology, our company specializes in providing high-quality biological products tailored for cutting-edge research. Our vast expertise in genetic engineering and cellular models positions us as a reliable partner for research endeavors aimed at unlocking the complexities of mitochondrial biology.
Please note that all services are for research use only. Not intended for any clinical use.
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