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EEF1AKMT2 Knockout Cell Lines

Gene: EEF1AKMT2

Official Full Name: EEF1A lysine methyltransferase 2provided by HGNC

Gene Summary: Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine methylation. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO05903 EEF1AKMT2 Knockout cell line (HeLa) Human EEF1AKMT2 1:3~1:6 Negative Online Inquiry
KO05904 EEF1AKMT2 Knockout cell line (HCT 116) Human EEF1AKMT2 1:2~1:4 Negative Online Inquiry
KO05905 EEF1AKMT2 Knockout cell line (HEK293) Human EEF1AKMT2 1:3~1:6 Negative Online Inquiry
KO05906 EEF1AKMT2 Knockout cell line (A549) Human EEF1AKMT2 1:3~1:4 Negative Online Inquiry

Background

EEF1AKMT2 Gene Knockout Cell Lines are a revolutionary tool in molecular biology research, specifically engineered to facilitate the functional studies of the EEF1AKMT2 gene, which encodes for an enzyme involved in protein synthesis. The gene knockout strategy involves the use of advanced techniques such as CRISPR-Cas9 to disrupt the endogenous EEF1AKMT2 gene, resulting in a complete loss of function. This allows researchers to assess the phenotypic consequences of EEF1AKMT2 deficiency, providing critical insights into its role in cellular processes, such as translational regulation and response to stress.

The primary function of EEF1AKMT2 is to facilitate the methylation of elongation factor 1-alpha (EF1A), which is crucial for proper protein translation. By creating knockout cell lines, researchers can study the resulting changes in cell behavior, signaling pathways, and overall cell physiology. This gene's involvement in various diseases, including cancer, emphasizes the importance of EEF1AKMT2 in therapeutic targets, making these knockout cell lines invaluable in both research and drug development settings.

Particularly appealing advantages of these cell lines include their high specificity and reproducibility, allowing for robust experimentation with fewer confounding variables compared to transient knockdown approaches. The well-characterized genetic alterations ensure that results can be reliably attributed to the loss of EEF1AKMT2 function. This precision is crucial for scientists exploring gene function or testing potential therapeutics.

Researchers and clinicians alike can derive substantial value from using EEF1AKMT2 Gene Knockout Cell Lines, as they enable a deeper understanding of the molecular underpinnings of diseases, leading to the development of innovative treatment strategies. Our company boasts a strong commitment to advancing biological research through high-quality, tailored tools such as these cell lines, backed by a team of experts dedicated to supporting scientific discovery.

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

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