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NR1H3 Knockout Cell Lines

Gene: NR1H3

Official Full Name: nuclear receptor subfamily 1 group H member 3provided by HGNC

Gene Summary: The protein encoded by this gene belongs to the NR1 subfamily of the nuclear receptor superfamily. The NR1 family members are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. This protein is highly expressed in visceral organs, including liver, kidney and intestine. It forms a heterodimer with retinoid X receptor (RXR), and regulates expression of target genes containing retinoid response elements. Studies in mice lacking this gene suggest that it may play an important role in the regulation of cholesterol homeostasis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00945 NR1H3 Knockout cell line(293T) Human NR1H3 1:3~1:6 Negative Online Inquiry
KO15639 NR1H3 Knockout cell line (HeLa) Human NR1H3 1:3~1:6 Negative Online Inquiry
KO15640 NR1H3 Knockout cell line (HCT 116) Human NR1H3 1:2~1:4 Negative Online Inquiry
KO15641 NR1H3 Knockout cell line (HEK293) Human NR1H3 1:3~1:6 Negative Online Inquiry
KO15642 NR1H3 Knockout cell line (A549) Human NR1H3 1:3~1:4 Negative Online Inquiry

Background

NR1H3 gene knockout cell lines are specifically engineered cellular models in which the NR1H3 gene, also known as liver X receptor alpha (LXRα), has been inactivated. These cell lines serve as powerful tools for studying the role of LXRα in various biological processes, including lipid metabolism, inflammation, and glucose homeostasis. This gene encodes a nuclear receptor that plays a crucial role in regulating cholesterol and fatty acid metabolism through its action as a transcription factor. By knocking out NR1H3, researchers can investigate the downstream metabolic consequences and the receptor's involvement in disease mechanisms such as atherosclerosis, diabetes, and obesity-related disorders.

The primary function of NR1H3 in cellular contexts involves the modulation of gene expression in response to oxysterols and other lipid derivatives. Upon ligand binding, LXRα forms heterodimers with retinoid X receptors, thus influencing transcriptional activity of target genes. The knockout of this gene allows scientists to delineate the regulatory pathways associated with NR1H3, offering insights into both normal physiological processes and pathophysiological conditions.

In research and clinical applications, NR1H3 knockout cell lines are invaluable for drug discovery, particularly in developing therapeutics targeting metabolic diseases. They provide an effective platform for screening potential LXR-modulating compounds, thus facilitating the identification of novel therapeutic agents. Compared to alternatives, such as wild-type cell lines, NR1H3 knockout models offer clear advantages by providing a controlled environment to study the absence of LXRα and its associated effects.

For researchers and clinicians focused on metabolic health, these cell lines represent a critical resource, enabling a deeper understanding of how the modulation of nuclear receptors can impact disease progression and treatment efficacy. Furthermore, our company brings extensive expertise in genetic engineering and cellular model development, ensuring that our NR1H3 knockout cell lines are of the highest quality and utility. This commitment to excellence empowers our customers to generate reliable data and translates into advancements in their research endeavors.

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

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