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Human Monoclonal CXCL1 Primary Antibody for 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. in The Journal of biological chemistry 2011
Show all 5 Pubmed References
Mouse (Murine) Polyclonal CXCL1 Primary Antibody for ELISA, WB - ABIN5693092
Zhang, Cao, Zhang, Ji, Gao: Chemokine contribution to neuropathic pain: respective induction of CXCL1 and CXCR2 in spinal cord astrocytes and neurons. in Pain 2013
Show all 4 Pubmed References
Human Polyclonal CXCL1 Primary Antibody for 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. in Journal of neuroinflammation 2014
Show all 4 Pubmed References
Mouse (Murine) Polyclonal CXCL1 Primary Antibody for 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. in 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 for 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. in Neurobiology of disease 2006
Human Monoclonal CXCL1 Primary Antibody for 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. in PLoS ONE 2018
Human Polyclonal CXCL1 Primary Antibody for 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. in Clinical cancer research : an official journal of the American Association for Cancer Research 2008
CXCL1 displays a specific microRNA (miR (show MLXIP Antibodies)) upregulated by the prototypical colon cancer onco-miR miR (show MLXIP Antibodies)-105.
These results show that AKIP1 (show AKIP1 Antibodies) is crucial in cervical cancer angiogenesis and growth by elevating the levels of the NF-kappaB (show NFKB1 Antibodies)-dependent chemokines CXCL1, CXCL2 (show CXCL2 Antibodies), and CXCL8 (show IL8 Antibodies).
Adipose stromal cells recruitment to tumours, driven by CXCL1 and CXCL8 (show IL8 Antibodies), promotes prostate cancer progression.
CXCL1, which is produced by breast cancer cells, can promote cancer growth and development
miR (show MLXIP Antibodies)-204 inhibits cell proliferation in gastric cancer by targeting CKS1B (show CKS1B Antibodies), CXCL1 and GPRC5A (show GPRC5A Antibodies).
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 (show TGFB1 Antibodies) were associated with thrombocytosis in IBC
the plasma concentrations of CXCL1 indicated the disease activity and prognosis in interstitial pneumonia with autoimmune features (IPAF (show NLRC4 Antibodies)). Thus, the CXCL1/CXCR2 (show CXCR2 Antibodies) axis appears to be involved in the progression of IPAF (show NLRC4 Antibodies).
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 (show ANPEP Antibodies) can promote h-JBMMSC chemotaxis by up-regulating CXCL1 and CXCL8 (show IL8 Antibodies)
Data suggest that CD4 (show CD4 Antibodies)+ T lymphocytes and microglial CD40 (show CD40 Antibodies) mediate their pro-nociceptive effects in part by promoting selected chemokine (show CCL1 Antibodies) responses, and more importantly, CXCL1 can play an anti-nociceptive role in peripheral nerve injury-induced neuropathic pain, which is possibly mediated by infiltrating neutrophils.
The results demonstrate that C57BL/6J mice have a functional defect in NLRP12 (show NLRP12 Antibodies), impaired CXCL1 production, and that macrophages require NLRP12 (show NLRP12 Antibodies) 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 (show CXCL2 Antibodies) in the production of anti-microbial peptides (beta-defensins), iNOS (show NOS2 Antibodies), NOX2 (show CYBB Antibodies) and pro-inflammatory molecules during mycobacterial infection of the host, is reported.
this study demonstrates that in vivo blocking of CXCL1 and CXCL2 (show CXCL2 Antibodies) can significantly reduce the Mycobacterium tuberculosis-induced bioactive IL-1beta (show IL1B Antibodies) production
RelA (show NFkBP65 Antibodies) has a role in regulating OIS in preneoplastic lesions; the RelA (show NFkBP65 Antibodies)/CXCL1/CXCR2 (show CXCR2 Antibodies) 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 (show IFNG Antibodies)) up-regulated interleukin 6 (IL-6 (show IL6 Antibodies)) and CXCL1 chemokine (show CCL1 Antibodies) (CXCL1) production of bone marrow mesenchymal stem cells (mBM-MSC (show MSC Antibodies)).
MMP7 (show MMP7 Antibodies) shedding of syndecan-1 (show SDC1 Antibodies)/CXCL1 complexes functions as a checkpoint that restricts neutrophil activation at sites of epithelial injury.
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