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anti-Human CSF2 Antibodies:
anti-Mouse (Murine) CSF2 Antibodies:
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Human Monoclonal CSF2 Primary Antibody for ELISA (Capture), FACS - ABIN4899319
Hirst, Hallsworth, Peng, Lee et al.: Selective induction of eotaxin release by interleukin-13 or interleukin-4 in human airway smooth muscle cells is synergistic with interleukin-1beta and is mediated by the interleukin-4 receptor ... in American journal of respiratory and critical care medicine 2002
Show all 4 references for ABIN4899319
Human Monoclonal CSF2 Primary Antibody for ELISA, WB - ABIN1724740
He, Shumansky, Connett, Anthonisen, Paré, Sandford: Association of genetic variations in the CSF2 and CSF3 genes with lung function in smoking-induced COPD. in The European respiratory journal 2008
Show all 3 references for ABIN1724740
Human Monoclonal CSF2 Primary Antibody for FACS - ABIN4895921
Alisa, Boswell, Pathan, Ayaru, Williams, Behboudi: Human CD4(+) T cells recognize an epitope within alpha-fetoprotein sequence and develop into TGF-beta-producing CD4(+) T cells. in Journal of immunology (Baltimore, Md. : 1950) 2008
Show all 2 references for ABIN4895921
Rat (Rattus) Monoclonal CSF2 Primary Antibody for FACS, ICC - ABIN4898951
Stojić-Vukanić, Nacka-Aleksić, Pilipović, Vujnović, Blagojević, Kosec, Dimitrijević, Leposavić: Aging diminishes the resistance of AO rats to EAE: putative role of enhanced generation of GM-CSF Expressing CD4+ T cells in aged rats. in Immunity & ageing : I & A 2015
Show all 2 references for ABIN4898951
Human Polyclonal CSF2 Primary Antibody for FACS, IF - ABIN654647
Stone, Vanderman, Willey, Long, Register, Shively, Stehle, Loeser, Ferguson: Osteoarthritic changes in vervet monkey knees correlate with meniscus degradation and increased matrix metalloproteinase and cytokine secretion. in Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2015
TRAF6 (show TRAF6 Antibodies) is also required for GM-CSF-induced ubiquitination and activation of Akt (show AKT1 Antibodies).
Data suggest that the methylotrophic yeast Pichia pastoris is an effective recombinant host for heterologous granulocyte-macrophage colony-stimulating factor (rhGM-CSF) production.
Letter: Knockdown of either filaggrin (show FLG Antibodies) or loricrin (show LOR Antibodies) increases the productions of interleukin (IL)-1alpha, IL-8 (show IL8 Antibodies), IL-18 (show IL18 Antibodies) and granulocyte macrophage colony-stimulating factor in stratified human keratinocytes.
Impaired RASGRF1 (show RASGRF1 Antibodies)/ERK (show EPHB2 Antibodies)-mediated GM-CSF response characterizes CARD9 (show CARD9 Antibodies) deficiency in French-Canadians.
Honokiol could possess potential anti-inflammatory effects and inhibits TNF-alpha (show TNF Antibodies)-induced IL-1beta (show IL1B Antibodies), GM-CSF and IL-8 (show IL8 Antibodies) production in PBMCs from rheumatoid arthritis patients.
The canonical NFkappaB (show NFKB1 Antibodies) signaling in fibroblasts, but not in tumor cells, was shown to be responsible for the induced and constitutive CSF2 expression.
GM-CSF primes IL-13 (show IL13 Antibodies) production by macrophages via PAR-2 (show F2RL1 Antibodies).
analysis of an IL2RA (show IL2RA Antibodies) polymorphism that controls GM-CSF production in human TH cells
NFKBIZ (show NFKBIZ Antibodies) gene knockdown in bronchial epithelial cells suppresses the release of IL-1b (show IL1B Antibodies)-induced IL-6 (show IL6 Antibodies) and GMCSF.
CFH (show CFH Antibodies) Y402H polymorphism is associated with elevated vitreal GM-CSF and choroidal macrophages in the postmortem human eye.
Influenza infection stimulates the secretion of IL-8 (show IL8 Antibodies) and GM-CSF by alveolar epithelial cells.
These results demonstrated that bovine colonic cells seem capable to respond to E. bovis merozoite I infection by the upregulation of CXCL10 (show CXCL10 Antibodies) and GM-CSF gene transcription.
Data suggest exposure to maternal CSF2 from D5-D7 of development is fundamentally different for female/male blastocysts with respect to embryo elongation, characteristics of transcriptome/methylome, and endometrial interferon tau secretion at D15 (show MRPL16 Antibodies).
The increase in calving rate caused by CSF2 treatment involves, in part, more extensive development of extraembryonic membranes and capacity of the conceptus to secrete IFNT2 at day 15 of pregnancy.
immunolocalization studies confirmed the presence of granulocyte-macrophage colony stimulating factor(GM-CSF) in the germ cell line in bovine and human testes and addition of GM-CSF enhances several parameters of sperm motility
the conceptus, through its secretion of IFN-tau, stimulates maternal epithelial expression of COX-2 (show PTGS2 Antibodies) and GM-CSF during the peri (show PLIN1 Antibodies)-attachment period in the cow.
CSF2 affect embryonic development and enhance embryo competence for posttransfer survival.
Evi1 (show MECOM Antibodies)(+)DA-3 cells modified to express an intracellular form of GM-CSF, acquired growth factor independence and transplantability and caused an overt leukemia in syngeneic hosts, without increasing serum GM-CSF levels.
IL-23 (show IL23A Antibodies)-induced GM-CSF mediates the pathogenicity of CD4 (show CD4 Antibodies)(+) T cells in experimental autoimmune myocarditis.
GM-CSF accelerated the G1/S phase transition in EPCs by upregulating the expression of cyclins D1 and E.
Proteomic Analysis Reveals Distinct Metabolic Differences Between Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) and Macrophage Colony Stimulating Factor (M-CSF (show CSF1R Antibodies)) Grown Macrophages Derived from Murine Bone Marrow Cells
host RNF13 (show RNF13 Antibodies) affects the concentration of GM-CSF in tumor-bearing lungs
Sc CW-derived BG stimulated the late and strong expression of Csf2 in a dectin-1 (show CLEC7A Antibodies)-dependent manner, they remain poor inducers of chemokine (show CCL1 Antibodies) and cytokine production in murine macrophages.
GM-CSF and uPA (show PLAU Antibodies) are required for Porphyromonas gingivalis-induced alveolar bone loss in a mouse periodontitis model.
These findings identify GM-CSF as central to the protective immune response that prevents progressive fungal disease
IL-23 (show IL23A Antibodies)/IL-1 (show IL1A Antibodies)/IFNgamma/TNFalpha (show TNF Antibodies)/T-bet/Eomesodermin (show EOMES Antibodies)-driven circuit drives GM-CSF/IFNgamma-producing Th17 cell development.
-12-modulated Th1 (show HAND1 Antibodies) cells readily produce IFN-gamma (show IFNG Antibodies) and GM-CSF in the CNS of mice and induce a severe form of EAE via an IL-23 (show IL23A Antibodies)-independent pathway.
CSF2 stimulates proliferation of trophectoderm cells by activation of the PI3K-and ERK1/2 (show MAPK1/3 Antibodies) MAPK (show MAPK1 Antibodies)-dependent MTOR (show FRAP1 Antibodies) signal transduction cascades.
Data indicate that differentially expressed IL-17 (show IL17A Antibodies), IL-22 (show IL22 Antibodies), and IL-23 (show IL23A Antibodies) levels are associated with K-ras (show HRAS Antibodies) in a stage-specific fashion along colorectal cancer progression and an association was established between mutant K-ras (show HRAS Antibodies) and GM-CSF and IFN-gamma (show IFNG Antibodies).
The protein encoded by this gene is a cytokine that controls the production, differentiation, and function of granulocytes and macrophages. The active form of the protein is found extracellularly as a homodimer. This gene has been localized to a cluster of related genes at chromosome region 5q31, which is known to be associated with interstitial deletions in the 5q- syndrome and acute myelogenous leukemia. Other genes in the cluster include those encoding interleukins 4, 5, and 13.
granulocyte-macrophage colony-stimulating factor
, colony stimulating factor 2 (granulocyte-macrophage)
, colony-stimulating factor
, granulocyte-macrophage colony stimulating factor 2
, put. GM-CSF
, granulate-macrophage stimulating factor
, granulocyte-macrophage stimulation factor