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FPR1 encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. Zusätzlich bieten wir Ihnen FPR1 Antikörper (117) und FPR1 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
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The data demonstrate that FPR1 is involved in neuroblastoma (zeige ARHGEF16 ELISA Kits) development and could represent a therapy option for the treatment of neuroblastoma (zeige ARHGEF16 ELISA Kits).
FAM3D plays a role in gastrointestinal homeostasis and inflammation through its receptors FPR1 and FPR2 (zeige FPR2 ELISA Kits).
Formylated MHC class Ib (zeige HLAF ELISA Kits) binding peptides activate both human and mouse neutrophils primarily through FPR1.
The inhibitory function of oxidant sensing by TRPM2 (zeige CLU ELISA Kits) requires the oxidation of Cys549, which then induces TRMP2 binding to formyl peptide receptor 1 (FPR1) and subsequent FPR1 internalization and signaling inhibition
FPR1 expression is significantly upregulated in human masticatory mucosa during wound healing
FAM19A4 (zeige FAM19A4 ELISA Kits) is a novel ligand of formyl peptide receptor 1.
The authors describe here the activation of isolated human blood neutrophils by TcdB and, moreover, by toxin fragments generated by limited proteolytical digestion via the FPR1 receptor.
these results highlight the importance of FPR1 in chemotherapy-induced anticancer immune responses.
Data suggest that formyl peptide receptor 1 (FPR1) stimulation may represent a novel therapeutic approach to counteract tumor angiogenesis.
a pepducin designed to target FPR1 was found to hijack FPR2 (zeige FPR2 ELISA Kits) and potently inhibit neutrophil functions
Intravital TPLSM revealed that formyl-peptide-FPR1 signaling is responsible for regulating neutrophil chemotaxis to allow migration into the necrotic area in hepatic ischemia-reperfusion injury
Formylated MHC class Ib binding peptides activate both human and mouse neutrophils primarily through FPR1.
Blocking of FPR1 completely abrogated the fMet-Leu-Phe-, gliadin- and synthetic peptide-induced migration.
Ovalbumininduced airway inflammation is mediated by upregulation of the TLR2 (zeige TLR2 ELISA Kits)/MyD88 (zeige MYD88 ELISA Kits)/NFkappaB signaling pathway and inhibition of LXA4R.
Deficiency of formyl peptide receptor 1 is associated with increased inflammation and enhanced liver injury after LPS (zeige TLR4 ELISA Kits)-stimulation
Fpr1/2 are critical for normal healing of the sterile skin wound by mediating the first wave of neutrophil infiltration.
these findings identify a novel role of FPR1 as pattern recognition receptors for perceiving the enteric microbiota that promotes repair of mucosal wounds via generation of reactive oxygen species from the enterocyte NOX1 (zeige NOX1 ELISA Kits).
FPR1 and FPR2 (zeige FPR2 ELISA Kits) play an important role in the innate immune responses against Streptococcus pneumoniae within the central nervous system and the lack of the receptors leads to a dysregulation of the inflammatory response compared with wild-type mice.
This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.
N-formylpeptide chemoattractant receptor
, fMLP receptor
, fMet-Leu-Phe receptor
, N-formyl peptide receptor
, lipoxin A4 receptor