Gene: MTR
Official Full Name: 5-methyltetrahydrofolate-homocysteine methyltransferaseprovided by HGNC
Gene Summary: This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36533 | MTR Knockout cell line (HeLa) | Human | MTR | 1:3~1:6 | Negative | Online Inquiry |
KO36534 | MTR Knockout cell line (HCT 116) | Human | MTR | 1:2~1:4 | Negative | Online Inquiry |
KO36535 | MTR Knockout cell line (HEK293) | Human | MTR | 1:3~1:6 | Negative | Online Inquiry |
KO36536 | MTR Knockout cell line (A549) | Human | MTR | 1:3~1:4 | Negative | Online Inquiry |
MTR Gene Knockout Cell Lines represent an innovative tool in molecular biology, specifically designed to investigate the role of the methionine synthase reductase (MTR) gene in various cellular functions. By employing CRISPR/Cas9 technology, these cell lines have been precisely engineered to lack functional MTR, allowing researchers to explore the gene’s contributions to cellular metabolism, epigenetic regulation, and response to oxidative stress.
The primary mechanism by which MTR Gene Knockout Cell Lines operate involves the disruption of the MTR pathway, which is vital for the conversion of homocysteine to methionine, a critical process in methylation reactions. By facilitating accurate studies of the metabolic consequences of MTR depletion, these cell lines provide insight into not only fundamental biological processes but also the pathophysiology of diseases linked to methylation imbalances, such as cancer and cardiovascular disorders.
The scientific importance of these cell lines extends into both research and clinical applications. They serve as valuable models for the investigation of gene function and regulatory networks, enabling breakthroughs in understanding complex diseases. Additionally, they offer unique prospects for the development of targeted therapeutics that address metabolic dysfunctions linked to MTR.
Compared to traditional knockout models, MTR Gene Knockout Cell Lines offer several advantages including enhanced efficiency in gene editing, the ability to derive multiple clonal lines for robust experimental validation, and comprehensive characterizations of cellular phenotypes. This specificity enables high-resolution studies that traditional methods often lack, thus optimizing experimental outcomes.
Researchers, clinicians, and pharmaceutical developers will find great value in utilizing MTR Gene Knockout Cell Lines, as the insights gained could drive forward the development of innovative therapeutic strategies. This product not only fosters breakthroughs in scientific understanding but also represents a significant leap toward addressing metabolic disorders at their genetic roots.
Our company is committed to advancing biological research through innovative tools like MTR Gene Knockout Cell Lines, leveraging our extensive expertise in gene editing technologies and cell line development to support researchers and clinicians in their quest for discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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