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  • mProX™ Human TLR6 Stable Cell Line

    [CAT#: S01YF-1023-PY212]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Immune Checkpoint Cell Lines

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    Product Information

    Target Family
    Immune Checkpoint
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1
    Target Classification
    Immune Checkpoint Cell Lines
    Target Research Area
    Infectious Research
    Related Diseases
    Leprosy 1; Multisystem Inflammatory Syndrome In Children
    Gene ID
    Human:10333
    UniProt ID
    Human:Q9Y2C9

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Toll-like receptor 6 (TLR6) is another member of the TLR family, known to recognize microbial lipopeptides in conjunction with TLR2. This recognition is crucial for the innate immune response against various pathogens, including bacteria and fungi. Polymorphisms in the TLR6 gene have been studied in various populations, revealing potential associations with susceptibility to certain infections. For instance, research has shown that Chinese Cantonese populations display distinct TLR6 polymorphisms, suggesting ethnic diversity in pathogen susceptibility. Furthermore, TLR6 has been implicated in the inflammatory response associated with certain tumors, providing a potential avenue for therapeutic interventions in cancer.

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    FAQ

    chat Casey Miller (Verified Customer)

    Does TLR6 play a role in viral infections? Nov 27 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    TLR6, along with other TLR monomers and heterodimers, has been shown to significantly inhibit the replication of enteroviruses like EV71, suggesting its role in antiviral innate responses. Nov 27 2020

    chat Casey Garcia (Verified Customer)

    Can TLR6 be targeted for cancer vaccine development? Nov 21 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    TLR6 has been identified as a significant participant in protein-protein interactions with potential vaccine constructs, indicating its relevance in eliciting immune responses against cancers such as colorectal cancer. Nov 21 2020

    Published Data

    Fig.1 TLR6 siRNAs reduce TLR6 mRNA and protein expression in HEK293/TLR2 cells.

    HEK293 constitutively expressing toll-like receptor 2 was utilized as an in vitro model system to investigate the efficacy and duration of gene knockdown achieved by RNA interference targeting the related pattern recognition receptor TLR6. On days 1 and 3 post-transfection of TLR6-specific small interfering RNAs versus non-targeting sequences, parallel analysis of cellular protein content was performed. Equivalent amounts of total protein isolated from experimental groups were fractionated electrophoretically and transferred to membranes prior to sequential incubated with primary antibodies raised against TLR6 or the housekeeping protein beta-actin, followed by horseradish peroxidase-conjugated secondary antibodies. Densitometric quantification of imaged immunoblots demonstrated robust yet transient silencing of TLR6 protein production in cells transfected with targeting versus non-targeting siRNAs. Further optimization of transfection protocols could potentiate more sustained ablation of TLR6 signaling without impacting cell viability or TLR2 expression.

    Ref: Chang, Serena, Angela Dolganiuc, and Gyongyi Szabo. "Toll-like receptors 1 and 6 are involved in TLR2-mediated macrophage activation by hepatitis C virus core and NS3 proteins." Journal of Leucocyte Biology 82.3 (2007): 479-487.

    Pubmed: 17595379

    DOI: 10.1189/jlb.0207128

    Research Highlights

    Bang, Sunghee. et al. "A Cardiolipin from Muribaculum intestinale Induces Antigen-Specific Cytokine Responses." Journal of the American Chemical Society, 2023.
    A systematic phenotypic screen of the mouse gut microbiome was conducted to identify metabolites with immunomodulatory properties. The screen discovered a total of 3,000 compounds with these characteristics. These results demonstrate the potential role of the gut microbiome in regulating the immune response. Further research can explore the mechanism of action and potential therapeutic applications of these metabolites. Overall, this study highlights the importance of the gut microbiome in maintaining immune homeostasis and its potential as a source of novel therapeutics.
    Bang, Sunghee. et al. "A Cardiolipin from Muribaculum intestinale Induces Antigen-Specific Cytokine Responses." Journal of the American Chemical Society, 2023.
    Pubmed: 37871232   DOI: 10.1021/jacs.3c09734

    Jun Park, Beom. et al. "Multiple toll-like receptors (TLRs) display differential bacterial and ligand specificity in the earthworm, Eisenia andrei." Journal of invertebrate pathology, 2023.
    The Toll-like receptors (TLRs) are a group of ancient and well-conserved pattern recognition receptors (PRRs) that can identify conserved pathogen-associated molecular patterns. They consist of three domains: an extracellular N-terminal domain with leucine-rich repeats (LRRs) for antigens, a type-I transmembrane domain, and an intracellular Toll/Interleukin-1 receptor (TIR) domain for downstream signaling. The authors have discovered six new full-length complementary DNA (cDNA) sequences, collectively known as Ean-TLR1/2/3/4/5/6, which contain a signal peptide, varying numbers of LRRs, and a TIR domain. Three conserved motifs, Box 1, Box 2, and Box 3, were identified within the TIR domain and are essential for downstream signaling. A phylogenetic analysis revealed two separate branches for earthworm TLRs: single cysteine cluster TLRs (sccTLRs) and multiple cysteine cluster TLRs (mccTLRs). Ean-TLRs 1/2/3/4 (sccTLRs) and Ean-TLR6 (mccTLRs) were found to be clustered with previously reported earthworm TLRs, as well as TLRs from other worm species. As PRRs, earthworm TLRs are capable of sensing a wide range of pathogens. While most earthworm TLRs were responsive to Gram-positive bacteria, only Ean-TLR3 did not show a response to any bacteria. This suggests that earthworms have the ability to distinguish between different species of Gram-positive bacteria through their TLR responses. Overall, the ligand specificity of earthworm TLRs suggests that their pathogen recognition is as diverse and specific as the mammalian TLR system.
    Jun Park, Beom. et al. "Multiple toll-like receptors (TLRs) display differential bacterial and ligand specificity in the earthworm, Eisenia andrei." Journal of invertebrate pathology, 2023.
    Pubmed: 37865158   DOI: 10.1016/j.jip.2023.108010

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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