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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. Additionally we are shipping FPR1 Antibodies (103) and FPR1 Proteins (5) and many more products for this protein.
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FPR1 expression is significantly upregulated in human masticatory mucosa during wound healing
FAM19A4 (show 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 (show FPR2 ELISA Kits) and potently inhibit neutrophil functions
the co-upregulated expression of mast cell chymase (show CMA1 ELISA Kits) and ANXA1 (show ANXA1 ELISA Kits)-FPR1 system in ectopic endometrium suggests their involvement in the development of endometriotic lesions.
FPR1 rs78488639 interacted with CFH (show CFH ELISA Kits) rs800292, HTRA1 (show HTRA1 ELISA Kits) rs11200638, and smoking, enhancing risk to exudative age-related macular degeneration and polypoidal choroidal vasculopathy .
These results demonstrate that a necroptosis pathway, likely mediated by annexin 1 (show ANXA1 ELISA Kits) acting through the FPR1 receptor, contributes to Stevens-Johnson syndrome (SJS (show HSPG2 ELISA Kits)) and toxic epidermal necrolysis.
A low FPR1/beta1 integrin co-localization was observed.
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 (show TLR2 ELISA Kits)/MyD88 (show 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 (show 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 (show NOX1 ELISA Kits).
FPR1 and FPR2 (show 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.
Further, these results reveal Fpr1 as a major mediator of host commensal interaction during dysbiosis.
The mechanism involved impaired early neutrophil recruitment to the liver with Fpr1 being sole receptor for neutrophils to sense Listeria chemoattractant signals and for production of bactericidal superoxide.
findings may have clinical significance because current smokers and subjects with emphysema showed increased FPR expression in bronchoalveolar fluids and on peripheral neutrophils
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