Recombinant Mouse TLR7 protein (Tagged)
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Recombinant Mouse TLR7 protein (Tagged) is a Mouse Fragment protein, in the 27 to 348 aa range, expressed in Mammalian, with >85%, suitable for SDS-PAGE.
View Alternative Names
Toll-like receptor 7, Tlr7
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Mouse TLR7 protein (Tagged) (AB267927)
SDS-PAGE analysis of recombinant Mouse TLR7 protein (ab267927)
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TLR7 induces an immune response by activating pathways that lead to the production of cytokines and type I interferons. It does not function alone but interacts within a complex involving other adaptors such as MyD88. This interaction initiates a signaling cascade that is essential for mounting an acute response to viral infections and boosting adaptive immunity.
Pathways
Single-stranded RNA detection through TLR7 activates the MyD88-dependent pathway which is important for innate immune responses. This pathway includes key components such as NF-κB and IRF7 leading to inflammatory cytokine production. TLR7 links with these proteins working together to activate the host defense mechanism against viral infections.
Specifications
Form
Liquid
General info
Function
Endosomal receptor that plays a key role in innate and adaptive immunity. Controls host immune response against pathogens through recognition of uridine-containing single strand RNAs (ssRNAs) of viral origin or guanosine analogs (PubMed : 21402738). Upon binding to agonists, undergoes dimerization that brings TIR domains from the two molecules into direct contact, leading to the recruitment of TIR-containing downstream adapter MYD88 through homotypic interaction. In turn, the Myddosome signaling complex is formed involving IRAK4, IRAK1, TRAF6, TRAF3 leading to activation of downstream transcription factors NF-kappa-B and IRF7 to induce pro-inflammatory cytokines and interferons, respectively (By similarity) (PubMed : 14976261).
Sequence similarities
Belongs to the Toll-like receptor family.
Post-translational modifications
The first cleavage is performed by asparagine endopeptidase or cathepsin family members. This initial cleavage event is followed by a trimming event that is solely cathepsin mediated and required for optimal receptor signaling.
Subcellular localisation
Endosome membrane
Target data
Product promise
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