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TRMT1 Knockout Cell Lines

Gene: TRMT1

Official Full Name: tRNA methyltransferase 1provided by HGNC

Gene Summary: This gene encodes a tRNA-modifying enzyme that acts as a dimethyltransferase, modifying a single guanine residue at position 26 of the tRNA. The encoded enzyme has both mono- and dimethylase activity when exogenously expressed, and uses S-adenosyl methionine as a methyl donor. The C-terminal region of the encoded protein has both a zinc finger motif, and an arginine/proline-rich region. Mutations in this gene have been implicated in autosomal recessive intellectual disorder (ARID). Alternative splicing results in multiple transcript variants encoding different isoforms. There is a pseudogene of this gene on the X chromosome. [provided by RefSeq, May 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO13026 TRMT1 Knockout cell line (HeLa) Human TRMT1 1:3~1:6 Negative Online Inquiry
KO13027 TRMT1 Knockout cell line (HCT 116) Human TRMT1 1:2~1:4 Negative Online Inquiry
KO13028 TRMT1 Knockout cell line (HEK293) Human TRMT1 1:3~1:6 Negative Online Inquiry
KO13029 TRMT1 Knockout cell line (A549) Human TRMT1 1:3~1:4 Negative Online Inquiry

Background

TRMT1 Gene Knockout Cell Lines are advanced cellular tools designed to elucidate the role of the TRMT1 (tRNA methyltransferase 1) gene in cellular processes. These genetically modified cell lines have been engineered to have a complete deletion of the TRMT1 gene, allowing for the specific study of its function in tRNA modification and its broader implications in genomic stability, mitochondrial function, and cellular stress responses.

The primary function of TRMT1 is to catalyze the methylation of adenine in specific tRNA molecules, which is critical for the stability and functionality of tRNA during protein synthesis. By utilizing these knockout cell lines, researchers can investigate the consequent biochemical pathways affected by the loss of TRMT1, offering insights into how tRNA modifications influence both normal physiology and disease states, such as cancer and metabolic disorders.

In the context of scientific importance, TRMT1 Gene Knockout Cell Lines provide a vital resource for both basic and applied research. They are particularly valuable for studying gene function through loss-of-function assays and exploring potential therapeutic targets related to tRNA dysregulation. In translational medicine, understanding TRMT1's role could pave the way for innovative treatments that restore tRNA methylation patterns and improve cellular function in pathological conditions.

Unlike conventional cell lines that may retain functional TRMT1, these knockout models offer a unique opportunity to observe direct effects resulting from the gene's absence, thus enhancing the accuracy of experimental outcomes. The targeted nature of this approach, combined with the high specificity of the knockout, ensures that the data generated are both reliable and relevant, setting these cell lines apart from standard alternatives.

For researchers and clinicians seeking to unravel the complexities of tRNA biology and its implications in health and disease, TRMT1 Gene Knockout Cell Lines represent an invaluable asset. They enable a deeper understanding of cellular mechanisms and contribute to the identification of novel therapeutic strategies.

Our company specializes in the development of cutting-edge biological products, focusing on genetic modifications and advanced cell line technologies to support the research community in uncovering the fundamental processes of life sciences. With a commitment to quality and innovation, we strive to empower your research with the tools needed to achieve groundbreaking discoveries.

Please note that all services are for research use only. Not intended for any clinical use.

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