Gene: TRMT1L
Official Full Name: tRNA methyltransferase 1Lprovided by HGNC
Gene Summary: This gene encodes a protein that has some similarity to N2,N2-dimethylguanosine tRNA methyltransferase from other organisms. Studies of the mouse ortholog have shown that this protein plays a role in motor coordination and exploratory behavior, and it may also be involved in modulating postnatal neuronal functions. Alternatively spliced transcripts have been identified for this gene. [provided by RefSeq, Jan 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO25682 | TRMT1L Knockout cell line (HeLa) | Human | TRMT1L | 1:3~1:6 | Negative | Online Inquiry |
KO25683 | TRMT1L Knockout cell line (HCT 116) | Human | TRMT1L | 1:2~1:4 | Negative | Online Inquiry |
KO25684 | TRMT1L Knockout cell line (HEK293) | Human | TRMT1L | 1:3~1:6 | Negative | Online Inquiry |
KO25685 | TRMT1L Knockout cell line (A549) | Human | TRMT1L | 1:3~1:4 | Negative | Online Inquiry |
TRMT1L Gene Knockout Cell Lines are genetically modified cell lines that have undergone targeted gene disruption of the TRMT1L gene, which encodes for a methyltransferase involved in the modification of tRNA molecules. The TRMT1L protein plays a crucial role in RNA metabolism by catalyzing the methylation of specific nucleotide residues in tRNA, which is vital for proper protein synthesis and cellular function. By creating knockout models, researchers can elucidate the functional significance of TRMT1L in various biological processes, including translational fidelity and cellular stress responses.
The mechanism of action behind the TRMT1L knockout involves the precise editing of the gene to eliminate its expression, allowing scientists to observe resulting phenotypic changes. These models are invaluable for studying the implications of TRMT1L in cellular mechanisms and disease states, making them significant tools in both fundamental research and translational studies. Their utility extends into cancer research, metabolic disorders, and exploring the relationship between tRNA modifications and mitochondrial dysfunction.
Compared to alternative models, such as wild-type or overexpressing systems, the TRMT1L Gene Knockout Cell Lines provide a more reliable platform for understanding loss-of-function effects. This specificity allows for the generation of clearer insights into molecular pathways, enabling researchers to draw more directed conclusions about TRMT1L's role in health and disease.
The value of incorporating TRMT1L knockout models into your research cannot be overstated; they facilitate groundbreaking studies that can lead to novel therapeutic targets and treatment strategies. Our company is dedicated to advancing scientific research by providing high-quality biological products, including precision-engineered cell lines that empower researchers and clinicians to unlock new avenues in their work.
Please note that all services are for research use only. Not intended for any clinical use.
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