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TLR3 Knockout Cell Lines

Gene: TLR3

Official Full Name: toll like receptor 3provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This receptor is most abundantly expressed in placenta and pancreas, and is restricted to the dendritic subpopulation of the leukocytes. It recognizes dsRNA associated with viral infection, and induces the activation of NF-kappaB and the production of type I interferons. It thus plays a role in host defense against multiple viruses. [provided by RefSeq, Jul 2021]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00213 TLR3 Knockout cell line (A549) Human TLR3 1:3~1:4 Negative Online Inquiry
KO00897 TLR3 Knockout cell line(A-431) Human TLR3 1:3~1:5 Negative Online Inquiry
KO13378 TLR3 Knockout cell line (HeLa) Human TLR3 1:3~1:6 Negative Online Inquiry
KO13379 TLR3 Knockout cell line (HCT 116) Human TLR3 1:2~1:4 Negative Online Inquiry

Background

TLR3 Gene Knockout Cell Lines are genetically modified cell lines that have had the TLR3 (Toll-like receptor 3) gene inactivated, allowing researchers to investigate the role of TLR3 in various biological processes. TLR3 is a pattern recognition receptor that plays a critical role in the innate immune response, particularly in recognizing double-stranded RNA, a common viral component. By utilizing TLR3 knockout cell lines, researchers can elucidate the pathways and mechanisms by which TLR3 mediates immune responses, contributing to a deeper understanding of host-pathogen interactions and the development of therapeutic interventions.

The key functionality of TLR3 Gene Knockout Cell Lines lies in their ability to enable targeted studies on immune signaling pathways. With the TLR3 gene disabled, researchers can evaluate the impact of TLR3 on cellular responses to viral infections, in a controlled environment devoid of TLR3 signaling. This allows for the exploration of alternative immune mechanisms that may be activated when TLR3 is absent, providing insights into compensatory pathways that cells may engage during infection.

Scientifically, TLR3 Gene Knockout Cell Lines are invaluable for both basic and applied research. They have significant implications in areas such as vaccine development, antiviral therapy, and the study of autoimmune diseases where aberrant TLR signaling may contribute to pathology. By analyzing the effects of TLR3 deletion, researchers can identify potential therapeutic targets or biomarkers to enhance patient outcomes in infectious and inflammatory diseases.

Compared to traditional cell lines, TLR3 Gene Knockout Cell Lines offer a unique advantage by providing clearer insights into the specific actions of TLR3 without confounding signals from other immune receptors. This specificity is critical for obtaining reliable data in experimental setups. Furthermore, the knockout approach is streamlined and can be used alongside other genetic editing techniques, creating a versatile platform for in-depth investigations.

For researchers and clinicians, these knockout cell lines represent a powerful tool to dissect the complexities of immune responses and to innovate novel therapeutic strategies. Our company specializes in the development of genetically modified cell lines, and our commitment to quality and scientific integrity ensures that each TLR3 Gene Knockout Cell Line is rigorously tested, characterized, and ready for your research needs. We provide comprehensive support to facilitate your studies, maximizing the potential of your research endeavors.

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

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