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Receptor for the chemotactic and inflammatory peptide anaphylatoxin C5a. Zusätzlich bieten wir Ihnen C5AR1 Antikörper (275) und C5AR1 Proteine (7) und viele weitere Produktgruppen zu diesem Protein an.
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Serum containing active complement enhanced pneumococcal induced proinflammatory cytokine production through C5a release and C5aR crosstalk.
C5a/C5aR pathway promotes gastric cancer pathogenesis by suppressing p21 (zeige CDKN1A ELISA Kits)/p-p21 (zeige CDKN1A ELISA Kits) expression via activation of PI3K (zeige PIK3CA ELISA Kits)/AKT (zeige AKT1 ELISA Kits) signaling.
C5aR plays a role in T helper cell polarization induced by Mycobacterium tuberculosis and this effect is strain- and donor-dependent.
Panton-Valentine leucotoxin LukS-PV/LukF-PV and the gamma-hemolysin (zeige PLC ELISA Kits) HlgC/HlgB, bind the C5a complement-derived peptide receptor, inducing intracellular calcium release in neutrophils.
Studies indicate that the complement response lie the active fragments, C3a (zeige C3 ELISA Kits) and C5a, acting through their specific receptors, C3aR (zeige C3AR1 ELISA Kits), C5aR1 and C5aR2 to direct the cellular response to inflammation.
TLR4 (zeige TLR4 ELISA Kits) and C5aR crosstalk in dendritic cells induces a core regulatory network of RSK2 (zeige RPS6KA3 ELISA Kits), PI3Kbeta, SGK1 (zeige SGK1 ELISA Kits), and FOXO (zeige FOXO3 ELISA Kits) transcription factors.
Results showed that 7-oxygenated cholesterol derivatives have differential effects on monocyte/macrophage expression of IL-8 (zeige IL8 ELISA Kits) and C5a receptor and that C5a receptor is involved in 7alphaOHChol-induced IL-8 (zeige IL8 ELISA Kits) expression via PI3K (zeige PIK3CA ELISA Kits) and MEK (zeige MAP2K1 ELISA Kits). Study demonstrated expression of IL-8 (zeige IL8 ELISA Kits) and C5a receptor primarily by 7alpha-hydroxycholesterol in monocytes/macrophages.
Reducing RPS19 (zeige RPS19 ELISA Kits) in tumor cells or blocking the C5a receptor 1-RPS19 (zeige RPS19 ELISA Kits) interaction decreases RPS19 (zeige RPS19 ELISA Kits)-mediated immunosuppression, impairs tumor growth, and delays the development of tumors in a transgenic model of breast cancer
C5aR expression in gastric cancer was associated with cancer progression, liver metastasis, and poor prognosis.
this study shows that downregulation of CD88 after stimulation with IL-8 (zeige IL8 ELISA Kits) is more pronounced in adults than in neonates, whereas fMLP (zeige FPR1 ELISA Kits) induces changes in receptor expression that are of the same magnitude in neutrophils from neonates as from adults
C5aR1 facilities the pathogenesis of chronic kidney infection by enhancement of bacterial colonization of tubular epithelium, promotion of local inflammatory responses, and impairment of phagocytic function of monocytes/macrophages.
Data indicate that complement component 5a receptor 1 protein (C5aR1) signaling in osteoblasts plays a detrimental role in bone regeneration after fracture.
The role of C5aR1 and C5aR2 in response to renal ischemia-reperfusion injury is reported. The results also demonstrated that C5aR2 is a functional receptor, rather than a decoy receptor, and may provide a new target for intervention.
these data reveal a differential role for C5aR during ethanol-induced liver inflammation and injury
These findings demonstrate a complex regulation pattern of C5aR1 in the airways, lung tissue and mediastinal lymph nodes of mice, suggesting that the C5a/C5aR1 axis controls airway constriction and inflammation through activation of myeloid cells in all three compartments in an experimental model of allergic asthma.
C5aR1-KO mice exhibited less renal injury, as evidenced by reduced albuminuria. In contrast, cardiac injury was accelerated with increased cardiac fibrosis and heart weight in C5aR1-deficient mice after ANG II (zeige AGT ELISA Kits) infusion. No effect was found on blood pressure. the C5a:C5aR1 axis drives end-organ damage in the kidney but protects from the development of cardiac fibrosis and hypertrophy in experimental hypertension.
This study demonstrated that C5aR1 contributes to the acute inflammatory response elicited by infiltrating immune cells following pilocarpine status epilepticus.
Regulation of complement 5a receptor (C5aR)-induced neutrophil chemotaxis via IgG1 immune complexes (ICs (zeige DNAI1 ELISA Kits)) depends on galectin-3 (zeige LGALS3 ELISA Kits).
The C5a/C5aR pathway is essential for up-regulating SphK1 (zeige SPHK1 ELISA Kits) expression through p38 MAPK (zeige MAPK14 ELISA Kits) activation in acute liver failure.in mice.
C5a bidirectionally amplifies TLR4 (zeige TLR4 ELISA Kits)-mediated NLRP3 (zeige NLRP3 ELISA Kits) inflammasome activation in monocytes while suppressing this pathway in macrophages. However, as C5aR1 deficiency attenuates the IL-1beta (zeige IL1B ELISA Kits) response to LPS (zeige TLR4 ELISA Kits) challenge in vivo, results suggest overall that C5a augments physiologic inflammasome responses.
Studies provide information regarding distinct structural and functional features that may contribute to the unique pharmacological properties of bovine C5aR.
Receptor for the chemotactic and inflammatory peptide anaphylatoxin C5a. This receptor stimulates chemotaxis, granule enzyme release and superoxide anion production.
C5a anaphylatoxin chemotactic receptor 1
, C5a anaphylatoxin receptor
, C5a ligand
, complement component 5 receptor 1
, complement component 5, receptor 1
, complement C5a receptor
, G protein-coupled receptor 77
, complement component 5 receptor 1 (C5a ligand)
, C5a anaphylatoxin chemotactic receptor
, anaphylatoxin C5a receptor
, complement component 5a receptor 1