
Toll-like receptor (TLR) NF-kB
Luciferase Reporter Cell Lines
The Toll-like receptor (TLR) family is a group of pattern-recognition receptors (PRRs) that play a central role in the innate immune system. TLRs detect pathogen-associated molecular patterns (PAMPs), such as viral nucleic acids, bacterial lipoproteins, and fungal components, enabling the immune system to respond rapidly to infections.
Each TLR recognizes specific molecular signatures:
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TLR2 detects bacterial lipoproteins and peptidoglycan.
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TLR3 senses double-stranded RNA from viruses.
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TLR4 recognizes lipopolysaccharide (LPS) from Gram-negative bacteria.
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TLR7 and TLR8 detect single-stranded RNA.
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TLR9 senses unmethylated CpG DNA.
Signosis offers a comprehensive collection of TLR/NF-κB luciferase reporter stable cell lines that enable real-time monitoring of pathway activation. These engineered cell models allow researchers to study ligand-induced NF-κB activation driven by individual TLRs—such as TLR2, TLR3, TLR4, TLR7, TLR8, and TLR9—with high sensitivity and reproducibility. With increasing focus on understanding innate immune activation, TLR specificity, and TRIF- or MyD88-dependent signaling mechanisms, our reporter systems provide a powerful platform for both basic immunology and translational drug discovery.
In addition to our cell line products, Signosis offers TLR/NF-κB functional screening services, providing researchers with a reliable solution for compound profiling, pathway characterization, and immunomodulatory drug screening.
Principle
Upon ligand recognition, TLRs activate intracellular signaling cascades, predominantly through the MyD88-dependent or TRIF-dependent pathways, leading to the activation of transcription factors such as NF-κB and IRFs (Interferon Regulatory Factors). This triggers the expression of pro-inflammatory cytokines, chemokines, and type I interferons, mounting a rapid and effective immune response.
Because of their pivotal role in innate immunity, antiviral defense, and inflammation, TLRs are widely studied in basic immunology research, drug discovery, and immunotherapy development. Leveraging this knowledge, our TLR/NF-κB stable reporter cell lines provide a robust platform for screening agonists, antagonists, and modulators of the TLR signaling pathways with high sensitivity and reproducibility

