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ELOVL4 Knockout Cell Lines

Gene: ELOVL4

Official Full Name: ELOVL fatty acid elongase 4provided by HGNC

Gene Summary: This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03768 ELOVL4 Knockout cell line (HeLa) Human ELOVL4 1:3~1:6 Negative Online Inquiry
KO03769 ELOVL4 Knockout cell line (HEK293) Human ELOVL4 1:3~1:6 Negative Online Inquiry
KO03770 ELOVL4 Knockout cell line (A549) Human ELOVL4 1:3~1:4 Negative Online Inquiry

Background

ELOVL4 Gene Knockout Cell Lines are specialized cellular models engineered to have a targeted disruption of the ELOVL4 gene, which encodes an enzyme critical for the elongation of very long-chain fatty acids. These mutation-specific cell lines serve as a powerful tool for studying the cellular functions and metabolic pathways associated with lipid metabolism and the resulting physiological implications. The ELOVL4 enzyme is particularly important in the synthesis of docosahexaenoic acid (DHA), vital for the development and function of photoreceptor cells in the retina.

The key mechanism of action in these knockout lines involves the ablation of ELOVL4 activity, leading to alterations in fatty acid composition and metabolism within the cells. This perturbation allows researchers to observe downstream effects, including changes in membrane fluidity, inflammatory responses, and apoptosis pathways. Such insights are invaluable for understanding the etiology of diseases linked to lipid metabolism disruptions, including certain inherited retinal dystrophies and systemic metabolic disorders.

The scientific importance of ELOVL4 Gene Knockout Cell Lines extends across various research and clinical applications, ranging from basic biology to drug discovery and developmental studies. They facilitate the exploration of disease models and therapeutic interventions in a controlled environment, enabling scientists to model human genetic diseases more accurately.

Compared to traditional cell lines, which might express functional ELOVL4, these knockout models provide unique advantages, including specificity for lipid-related research and the ability to directly manipulate metabolic pathways. Additionally, they serve as an excellent platform for high-throughput screening of compounds that could restore the function of lipid metabolic processes affected by genetic mutations.

For researchers and clinicians focused on metabolic diseases or retinal health, these cell lines represent a critical resource, offering a robust foundation for innovative studies that could lead to groundbreaking therapies. Our company has a longstanding commitment to providing high-quality biological reagents, supported by rigorous validation processes and extensive technical expertise in cell line development. This ensures that our ELOVL4 Gene Knockout Cell Lines meet the highest standards necessary for cutting-edge scientific inquiry.

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

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