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CXCR3 encodes a G protein-coupled receptor with selectivity for three chemokines, termed CXCL9/Mig (monokine induced by interferon-g), CXCL10/IP10 (interferon-g-inducible 10 kDa protein) and CXCL11/I-TAC (interferon-inducible T cell a-chemoattractant). Zusätzlich bieten wir Ihnen CXCR3 Antikörper (313) und CXCR3 Proteine (10) und viele weitere Produktgruppen zu diesem Protein an.
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Human CXCR3 ELISA Kit für Sandwich ELISA - ABIN366833
Zhang, Liu, Su, Shi, Chen: Serum fractalkine and interferon-gamma inducible protein-10 concentrations are early detection markers for acute renal allograft rejection. in Transplantation proceedings 2014
High CXCR3 expression is associated with invasion and metastasis in tongue squamous cell carcinoma.
Up-regulated CXCR3 is detectable in the amniotic fluid and associated with the presence of placental lesions consistent with maternal anti-fetal rejection so may serve as a potential marker of spontaneous preterm delivery.
the expression of chemokine (zeige CCL1 ELISA Kits) receptors in different peripheral blood T-cell subsets in patients with polymyositis (PM) and dermatomyositis, was examined.
Results suggest that infiltration of chemokine (C-X-C motif) receptor 3 (CXCR3)-positive plasma cells is a characteristic feature of Hunner type interstitial cystitis (HIC).
Results of this study indicate that CXCR3 overexpression in GC is associated with increased DC and TIL (zeige TLR1 ELISA Kits) infiltration and improved OS.
Following activation with T-cell receptor and co-culture with various concentrations of chrysotile fibers using freshly isolated CD4 (zeige CD4 ELISA Kits)+ surface CXCR3 positive and negative fractions, the intracellular expression of CXCR3, IFNgamma and IL-17 (zeige IL17A ELISA Kits) remained unchanged when co-cultured with chrysotile.
In conclusion, it seems that decreased expression of CXCR3 and higher expression of CCR6 (zeige CCR6 ELISA Kits) were associated with HTLV-1 infection, what indicate that these alterations may favor virus dissemination but not disease manifestation.
Alternatively spliced variant of CXCR3 mediates the metastasis of liver cancer.
The CXCL4 (zeige PF4 ELISA Kits) monomer acts as the minimal active unit for interacting with CXCR3 N-Terminal Sulfated (zeige SULF1 ELISA Kits) Peptide, and sulfation of N-terminal tyrosine residues on the receptor is important for binding.
approach has been able to describe the structural events which dynamically characterize the molecular mechanisms involved in the binding of CXCR3 to CXCL11 (zeige CXCL11 ELISA Kits) and the critical role exerted by its N-terminal region in "hunting" and capturing the ligand.
The data of this study suggested that spinal CXCR3 mediates chronic itch and alloknesis, and targeting CXCR3 may provide effective treatment for chronic pruritus.
Study provided the evidence that CXCL10 (zeige CXCL10 ELISA Kits)/CXCR3 signaling in periaqueductal gray is involved in the development of morphine analgesic tolerance via neuron-microglia interaction.
The results demonstrate that the recruitment of peripheral immune cells into the CNS, induction of neuroinflammation, and consecutive weight loss during herpes encephalitis is modulated by CXCR3 signaling.
results show an important role for CXCR3 and CXCL10 (zeige CXCL10 ELISA Kits) in the tissue distribution of preimmune memory phenotype CD8 (zeige CD8A ELISA Kits) T- cells
Our data suggests that the altered gene profiles induced by CXCR3 deficiency promotes autoimmune cholangitis through pathogenic CD8 (zeige CD8A ELISA Kits)(+) T cells.
Data suggest that the CXCL9 (zeige CXCL9 ELISA Kits)-CXCR3 axis plays a pivotal role in the liver-specific distribution of TRAIL+ NK cells in mice.
ATF3 (zeige ATF3 ELISA Kits)-KO mice escape from PE-dependent maladaptive cardiac remodeling by suppressing the IFNgamma-CXCL10 (zeige CXCL10 ELISA Kits)-CXCR3 axis at multiple levels.
study thus shows that lung mucosal-resident memory T cells are not generated following systemic TB immunization and that local inflammation is required for systemically activated T cells to home to lung mucosa, which is mediated by interaction between CXCR3 upregulated in these cells and its ligands IP-10 (zeige CXCL10 ELISA Kits) and MIG (zeige CXCL9 ELISA Kits)
Antigen targeting to DEC-205 (zeige LY75 ELISA Kits) on dendritic cells leads to an IL-10 (zeige IL10 ELISA Kits)-dependent downregulation of CXCR3 expression on differentiated antigen-specific Th1 (zeige HAND1 ELISA Kits) cells in vivo. This downregulation interferes with the migration of Th1 (zeige HAND1 ELISA Kits) cells into the gut (zeige GUSB ELISA Kits) and protects mice against severe acute and relapsing intestinal inflammation.
this study shows that neutrophils and NK cells act as important disease-promoting immune cells in experimental osteoarthritis and their functional interaction is promoted by the CXCL10 (zeige CXCL10 ELISA Kits)/CXCR3 axis
Transcript analysis showed that antigen stimulation of WC1(+)gammadelta T cells substantially increased CXCR3 expression
The demonstration of a conserved CXCR3-CXCL11 (zeige CXCL11 ELISA Kits) signaling axis in zebrafish extends the translational applicability of this model for studying diseases involving the innate immune system.
This gene encodes a G protein-coupled receptor with selectivity for three chemokines, termed CXCL9/Mig (monokine induced by interferon-g), CXCL10/IP10 (interferon-g-inducible 10 kDa protein) and CXCL11/I-TAC (interferon-inducible T cell a-chemoattractant). Binding of chemokines to this protein induces cellular responses that are involved in leukocyte traffic, most notably integrin activation, cytoskeletal changes and chemotactic migration. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. One of the isoforms (CXCR3-B) shows high affinity binding to chemokine, CXCL4/PF4 (PMID:12782716).
C-X-C chemokine receptor type 3
, G protein-coupled receptor 9
, IP-10 receptor
, IP10 receptor
, Mig receptor
, chemokine (C-X-C) receptor 3
, interferon-inducible protein 10 receptor
, chemokine (C-X-C motif) receptor 3
, CXC chemokine receptor 3
, Interferon-inducible protein 10 receptor
, chemokine (C-X-C motif) receptor 3.1