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The protein encoded by CCR3 is a receptor for C-C type chemokines. Additionally we are shipping CCR3 Antibodies (319) and CCR3 Kits (13) and many more products for this protein.
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the expression of CCR3 on dispersed synovial tissue and peripheral blood cells in rheumatoid arthritis, was investigated.
Chemokine (show CCL1 Proteins) receptors CCR3 and CCR4 (show CCR4 Proteins), and the mucosa specific chemokine (show CCL1 Proteins) CCL28 (show ENC1 Proteins) have predominant roles in oral wound healing by increasing human gingiva fibroblast proliferation, migration, and the secretion of IL-6 (show IL6 Proteins) and HGF (show HGF Proteins) and reducing the secretion of TIMP-1 (show TIMP1 Proteins).
simvastatin was demonstrated to inhibit IL-5 (show IL5 Proteins)-induced CCR3 expression and chemotaxis of eosinophils mediated via the mevalonate pathway.
Data indicate that approximately 4.5% dispersed osteoarthritis (OA) synovial tissue cells are CC chemokine receptor CCR 3 (CCR3)+ cells.
This meta-analysis provides robust estimates that interleukin 18 receptor accessory protein (show IL18RAP Proteins) rs917997 and chemokine (C-C motif) receptor 3 rs6441961 are potential risk factors for celiac disease in European populations.
Results highlight the potential role of CCR (show POR Proteins) genes in narcolepsy and support the hypothesis that patients with narcolepsy have impaired immune function.
Periprostatic adipocytes drive prostate cancer progression in obesity via CCL7 (show CCL7 Proteins) secretion which stimulates CCR3 expressing tumor cells.
Results show the structure of CCL11 bound to the sulfated (show SULF1 Proteins) N-terminal region of its receptor CCR3 and show that intact CCR3 is sulfated (show SULF1 Proteins) and sulfation enhances receptor activity.
CCL28 (show ENC1 Proteins)-CCR3 interactions are involved in the homeostatic trafficking of CD4 (show CD4 Proteins)(+) T cells to the upper airways.
In vitro chemotaxis assay indicates dominant role of RANTES and IP-10 in the selective recruitment of CXCR3(+)CCR5(+)cells at the tubercular pathologic sites.
Retinal inhibition of CCR3 induces retinal cell death in a murine model of choroidal neovascularization.
The RNA interference therapy to CCR3 by local administration pernasal can suppress the process of the development, migration and invasion of the allergic rhinitis eosinophil.
Chemokine (show CCL1 Proteins) CCR3 ligands-binding peptides derived from a random phage-epitope library.
CCR3 plays no role in choroidal neovascularization development.
The collective data suggest that activation of the CB2R (show CNR2 Proteins) results in "cross-talk" with CCR-3, resulting in decreased migratory responsiveness to Tat (show TAT Proteins).
CCR3 plays no significant role in choroidal neovascularization development.
The CCR3/eotaxin pathway is involved in the regulation of allergen-driven in situ haematopoiesis and the accumulation/mobilization of eosinophil-lineage-committed progenitor cells in the lung.
Trafficking to the cell surface of nascent CCR3 is critically dependent on a C-terminal leucine residue, suggestive of specific mechanisms for CCR3 export.
CCR3-deficiency does not alter mast cell phenotype or ability to migrate in vitro
The expression of CCR3 in the bone marrow and peripheral tissue with allergic asthma was significantly higher than that in the controls.
The protein encoded by this gene is a receptor for C-C type chemokines. It belongs to family 1 of the G protein-coupled receptors. This receptor binds and responds to a variety of chemokines, including eotaxin (CCL11), eotaxin-3 (CCL26), MCP-3 (CCL7), MCP-4 (CCL13), and RANTES (CCL5). It is highly expressed in eosinophils and basophils, and is also detected in TH1 and TH2 cells, as well as in airway epithelial cells. This receptor may contribute to the accumulation and activation of eosinophils and other inflammatory cells in the allergic airway. It is also known to be an entry co-receptor for HIV-1. This gene and seven other chemokine receptor genes form a chemokine receptor gene cluster on the chromosomal region 3p21. Alternatively spliced transcript variants have been described.
, C-C chemokine receptor type 3
, CC chemokine receptor 3
, b-chemokine receptor
, eosinophil CC chemokine receptor 3
, eosinophil eotaxin receptor
, MIP-1 alpha RL2
, MIP-1 alphaRL2
, chemokine (C-C) receptor 1,-like 2
, chemokine (C-C) receptor 3
, macrophage inflammatory protein 1-alpha receptor-like 2
, probable C-C chemokine receptor type 3
, C-C chemokine receptor 3
, eotaxin receptor CCR3