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Human Monoclonal CXCL1 Primary Antibody pour CyTOF, ELISA (Capture) - ABIN4900740
Meen, Øynebråten, Reine, Duelli, Svennevig, Pejler, Jenssen, Kolset: Serglycin is a major proteoglycan in polarized human endothelial cells and is implicated in the secretion of the chemokine GROalpha/CXCL1. dans The Journal of biological chemistry 2011
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Human Polyclonal CXCL1 Primary Antibody pour WB - ABIN3044150
Xu, Zhu, Zhang, Tian, Zhang, Wu, Gao: NF?B-mediated CXCL1 production in spinal cord astrocytes contributes to the maintenance of bone cancer pain in mice. dans Journal of neuroinflammation 2014
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Mouse (Murine) Polyclonal CXCL1 Primary Antibody pour IF (p), IHC (p) - ABIN2173443
Ito, Katano, Kawai, Yagoto, Takahashi, Ka, Ogura, Takahashi, Ito: A Novel Xenogeneic Graft-Versus-Host Disease Model for Investigating the Pathological Role of Human CD4(+) or CD8(+) T Cells Using Immunodeficient NOG Mice. dans American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2016
Rat (Rattus) Polyclonal CXCL1 Primary Antibody pour Func, ELISA - ABIN2473131
Vallès, Grijpink-Ongering, de Bree, Tuinstra, Ronken: Differential regulation of the CXCR2 chemokine network in rat brain trauma: implications for neuroimmune interactions and neuronal survival. dans Neurobiology of disease 2006
Human Monoclonal CXCL1 Primary Antibody pour FACS, IHC (fro) - ABIN151355
Traister, Patel, Huang, Patel, Plakhotnik, Lee, Medina, Welsh, Ruparel, Zhang, Friedberg, Maynes, Coles: Cardiac regenerative capacity is age- and disease-dependent in childhood heart disease. dans PLoS ONE 2018
Human Polyclonal CXCL1 Primary Antibody pour ELISA - ABIN4274952
Kawanishi, Matsui, Ito, Watanabe, Takahashi, Nishizawa, Nishiyama, Kamoto, Mikami, Tanaka, Jung, Akiyama, Nobumasa, Guilford, Reeve, Okuno, Tsujimoto, Nakamura, Ogawa: Secreted CXCL1 is a potential mediator and marker of the tumor invasion of bladder cancer. dans Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Adipose stromal cells recruitment to tumours, driven by CXCL1 and CXCL8 (Montrer IL8 Anticorps), promotes prostate cancer progression.
CXCL1, which is produced by breast cancer cells, can promote cancer growth and development
miR (Montrer MLXIP Anticorps)-204 inhibits cell proliferation in gastric cancer by targeting CKS1B (Montrer CKS1B Anticorps), CXCL1 and GPRC5A (Montrer GPRC5A Anticorps).
Thrombocytosis was more prevalent in patients with inflammatory breast cancer (IBC)than in those with non-IBC and it was associated with poor prognosis. GRO and TGF-beta (Montrer TGFB1 Anticorps) were associated with thrombocytosis in IBC
the plasma concentrations of CXCL1 indicated the disease activity and prognosis in interstitial pneumonia with autoimmune features (IPAF (Montrer NLRC4 Anticorps)). Thus, the CXCL1/CXCR2 (Montrer CXCR2 Anticorps) axis appears to be involved in the progression of IPAF (Montrer NLRC4 Anticorps).
CXCL1/8 secreted by adipose-derived mesenchymal stem cells could promote breast cancer angiogenesis.
GROA overexpression is associated with invasion in triple negative breast cancer.
The results of the transwell chemotaxis assay also supported the above results. Our data suggest that APN (Montrer ANPEP Anticorps) can promote h-JBMMSC chemotaxis by up-regulating CXCL1 and CXCL8 (Montrer IL8 Anticorps)
This study highlighted CAF (Montrer KAT2B Anticorps)-secreted CXCL1 as an attractive target to reverse tumor radioresistance.
we identified the microRNA miR (Montrer MLXIP Anticorps)-200a as a putative post-transcriptional regulator of CXCL1 in hepatocellular carcinoma
The results demonstrate that C57BL/6J mice have a functional defect in NLRP12 (Montrer NLRP12 Anticorps), impaired CXCL1 production, and that macrophages require NLRP12 (Montrer NLRP12 Anticorps) expression for effective recruitment of neutrophils to inflammatory sites.
GAG interactions and receptor activity of CXCL1 monomers and dimers are fine-tuned to regulate neutrophil trafficking for successful resolution of tissue injury.
a paracrine role for Hippo-mediated secretion of CXCL1 and CXCL2 (Montrer CXCL2 Anticorps) in the production of anti-microbial peptides (beta-defensins), iNOS (Montrer NOS2 Anticorps), NOX2 (Montrer CYBB Anticorps) and pro-inflammatory molecules during mycobacterial infection of the host, is reported.
this study demonstrates that in vivo blocking of CXCL1 and CXCL2 (Montrer CXCL2 Anticorps) can significantly reduce the Mycobacterium tuberculosis-induced bioactive IL-1beta (Montrer IL1B Anticorps) production
RelA (Montrer NFkBP65 Anticorps) has a role in regulating OIS in preneoplastic lesions; the RelA (Montrer NFkBP65 Anticorps)/CXCL1/CXCR2 (Montrer CXCR2 Anticorps) 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 (Montrer IFNG Anticorps)) up-regulated interleukin 6 (IL-6 (Montrer IL6 Anticorps)) and CXCL1 chemokine (Montrer CCL1 Anticorps) (CXCL1) production of bone marrow mesenchymal stem cells (mBM-MSC (Montrer MSC Anticorps)).
MMP7 (Montrer MMP7 Anticorps) shedding of syndecan-1 (Montrer SDC1 Anticorps)/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 (Montrer MMP3 Anticorps)) repressed the upregulation of the chemokines monocyte chemoattractant protein (MCP)-1 (Montrer CPT1B Anticorps) and (C-X-C motif) ligand 1 (CXCL1).
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.
C-X-C motif chemokine 1
, GRO1 oncogene (melanoma growth stimulating activity, alpha)
, GRO1 oncogene (melanoma growth-stimulating activity)
, MGSA alpha
, fibroblast secretory protein
, growth-regulated alpha protein
, melanoma growth stimulatory activity alpha
, neutrophil-activating protein 3
, chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha)
, cytokine-induced neutrophil chemoattractant 1
, platelet-derived growth factor-inducible protein KC
, chemokine CXCL1/GRO-ALPHA
, melanoma growth stimulatory activity homolog
, growth related gene 1
, growth-regulated protein homolog alpha
, GRO1 oncogene
, secretory protein N51
, growth regulated protein GRO
, growth regulated