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this study demonstrates that in vivo blocking of CXCL1 and CXCL2 (zeige CXCL2 Proteine) can significantly reduce the Mycobacterium tuberculosis-induced bioactive IL-1beta (zeige IL1B Proteine) production
RelA (zeige NFkBP65 Proteine) has a role in regulating OIS in preneoplastic lesions; the RelA (zeige NFkBP65 Proteine)/CXCL1/CXCR2 (zeige CXCR2 Proteine) axis is an essential mechanism of tumor surveillance in pancreatic ductal adenocarcinoma
CXCL1 contributed to rapid neutrophil recruitment during Bacillus cereus endophthalmitis. In CXCL1-knockout mice, retinal function was greater and neutrophil influx was less than in control mice, confirming its role in ocular inflammation.
Interferon-gamma (IFN-gamma (zeige IFNG Proteine)) up-regulated interleukin 6 (IL-6 (zeige IL6 Proteine)) and CXCL1 chemokine (zeige CCL1 Proteine) (CXCL1) production of bone marrow mesenchymal stem cells (mBM-MSC (zeige MSC Proteine)).
MMP7 (zeige MMP7 Proteine) shedding of syndecan-1 (zeige SDC1 Proteine)/CXCL1 complexes functions as a checkpoint that restricts neutrophil activation at sites of epithelial injury.
Data show that loss of loss of matrix metalloproteinase-3 (MMP-3 (zeige MMP3 Proteine)) repressed the upregulation of the chemokines monocyte chemoattractant protein (MCP)-1 (zeige CPT1B Proteine) and (C-X-C motif) ligand 1 (CXCL1).
CXCR2 (zeige CXCR2 Proteine)/CXCL1 axis promotes granulocytic myeloid-derived suppressor cells recruitment and facilitates arginase I (zeige ARG1 Proteine) expression and activity of these cells at maternal-fetal interface
The novel findings reveal the critical role of NLRP12 (zeige NLRP12 Proteine)-IL-17A (zeige IL17A Proteine)-CXCL1 axis in host defense by modulating neutrophil recruitment against Klebsiella pneumoniae.
Nlrp12 (zeige NLRP12 Proteine) deficiency caused increased neutrophil migration towards the chemokine (zeige CCL1 Proteine) CXCL1 and the neutrophil parasite Leishmania major, revealing NLRP12 (zeige NLRP12 Proteine) as a negative regulator of directed neutrophil migration under these conditions.
CXCL1 monomer-dimer distribution and receptor interactions are highly coupled and regulate neutrophil trafficking and that injury in the context of disease is a consequence of inappropriate CXCR2 (zeige CXCR2 Proteine) activation
Taken together, the present study indicates that IL-33 (zeige IL33 Proteine) localized in the human atherosclerotic plaque increases GRO-alpha mRNA expression and protein secretion via activation of ERK1/2, JNK (zeige MAPK8 Proteine), and NF-kappaB (zeige NFKB1 Proteine) in HUVECs, suggesting that IL-33 (zeige IL33 Proteine) plays an important role in the pathophysiology and development of atherosclerosis.
Study provides the first evidence that primary malignant cell-secreted VEGFA (zeige VEGFA Proteine) stimulates tumor-associated macrophages to produce CXCL1, which recruits CXCR2 (zeige CXCR2 Proteine)-positive MDSCs to form a premetastatic niche to promote liver metastases.
the presence of elevated circulating levels of VEGF (zeige VEGFA Proteine) and CXCL1 are predictive of liver and lung metastasis, respectively of colorectal cancer.
This study describe elevated levels of CXCL1 and it receptor in the Solid Component and Cyst Fluid of Human Adamantinomatous Craniopharyngioma, relative to other pediatric brain tumors and normal cerebral tissue.
The expressions of CXCL1 in cancer cells and CXCR2 (zeige CXCR2 Proteine) in stromal cells are useful prognostic factors for gastric cancer patients
CXCL1 secreted by tumor-associated lymphatic endothelial cells promotes lymph node metastasis of gastric cancer through integrin beta1/FAK (zeige PTK2 Proteine)/AKT (zeige AKT1 Proteine) signaling pathway.
S100A9 (zeige S100A9 Proteine) and S100A12 (zeige S100A12 Proteine) may have a role in the pathogenesis of pneumonia: S100A9 (zeige S100A9 Proteine) and CXCL1 may contribute solely in mild pneumonia, and CCL5 (zeige CCL5 Proteine) and CXCL11 (zeige CXCL11 Proteine) may contribute in severe pneumonia.
These findings support a role for CXCL1 and IL-8 (zeige IL8 Proteine) in cystic fibrosis (zeige S100A8 Proteine) lung disease severity and identify STAT3 (zeige STAT3 Proteine) as a modulating pathway.
Results suggest that CXCL1 is a key molecular link between senescence of stromal fibroblasts and tumor growth.
Increased IL-8 and CXCL1 transcription in T84 and THP-1 cells compared to that in wild-type EPEC.
This gene encodes a member of the CXC subfamily of chemokines. The encoded protein is a secreted growth factor that signal through the G-protein coupled receptor, CXC receptor 2. This protein plays a role in inflammation and as a chemoattractant for neutrophils. Aberrant expression this protein is associated with the growth and progression of certain tumors. A naturally occurring processed form of this protein has increased chemotactic activity. Alternate splicing results in coding and non-coding variants of this gene. A pseudogene of this gene is found on chromosome 4.
, growth-regulated alpha protein
, chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha)
, melanoma growth stimulatory activity homolog
, C-X-C motif chemokine 1
, cytokine-induced neutrophil chemoattractant 1
, platelet-derived growth factor-inducible protein KC
, GRO1 oncogene
, secretory protein N51
, growth regulated protein GRO
, growth regulated
, GRO1 oncogene (melanoma growth stimulating activity, alpha)
, GRO1 oncogene (melanoma growth-stimulating activity)
, MGSA alpha
, fibroblast secretory protein
, melanoma growth stimulatory activity alpha
, neutrophil-activating protein 3
, growth related gene 1
, growth-regulated protein homolog alpha