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ELAVL4 Knockout Cell Lines

Gene: ELAVL4

Official Full Name: ELAV like RNA binding protein 4provided by HGNC

Gene Summary: Enables mRNA 3'-UTR AU-rich region binding activity; poly(A) binding activity; and pre-mRNA intronic pyrimidine-rich binding activity. Involved in 3'-UTR-mediated mRNA stabilization; RNA processing; and positive regulation of 3'-UTR-mediated mRNA stabilization. Predicted to be located in axon; cytoplasm; and dendrite. Predicted to be part of ribonucleoprotein complex. Predicted to be active in glutamatergic synapse. [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
KO00066 ELAVL4 Knockout cell line (H1) Human ELAVL4 1:6-1:8 Negative Online Inquiry

Background

ELAVL4 Gene Knockout Cell Lines are specifically engineered cellular models designed for the study of the ELAVL4 gene, also known as HuD, which plays a critical role in post-transcriptional regulation of mRNA stability and translation. By utilizing CRISPR-Cas9 technology, these cell lines provide researchers with a powerful tool to investigate the functional consequences of ELAVL4 gene disruption in various biological processes, including neuronal development, synaptic plasticity, and cellular response to stress.

The key function of the ELAVL4 knockout cell lines lies in their ability to mimic the loss of ELAVL4 expression in a controlled environment, thus enabling scientists to systematically assess changes in gene expression, protein synthesis, and cellular behavior. This is particularly valuable in neurobiological research, where ELAVL4 is implicated in neurological disorders such as amyotrophic lateral sclerosis (ALS) and Alzheimer's disease. By observing the phenotypic and molecular changes in these knockout models, researchers can gain deeper insights into the pathophysiological mechanisms underlying these diseases.

In both research and clinical settings, the significance of ELAVL4 knockout cell lines cannot be overstated. They offer a unique platform to screen potential therapeutic compounds and to validate targets for drug development focused on diseases associated with ELAVL4 dysregulation. The specificity of these models allows for high-throughput screening applications, which are essential for the rapid identification of new treatment strategies.

Compared to alternative gene editing models, such as transient knockdown methods or less specific models, the ELAVL4 knockout cell lines provide a stable, reliable, and reproducible system with long-term expression profiles. This stability offers significant advantages for both basic research and translational applications, allowing for consistent results over extended study durations.

For researchers and clinicians seeking to understand the nuances of ELAVL4-related pathways, these knockout cell lines represent a critical asset in their toolkit. They enable studies that bridge fundamental biology with clinical implications, facilitating the advancement of therapeutic approaches.

Our company specializes in high-quality biological products that empower researchers in genomics and molecular biology. With a solid foundation in innovative gene-editing technologies and an unwavering commitment to scientific excellence, we offer an extensive range of genetically modified models designed to meet the evolving needs of the research community.

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

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