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anti-Human EPO Antibodies:
anti-Rat (Rattus) EPO Antibodies:
anti-Mouse (Murine) EPO Antibodies:
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Mouse (Murine) Monoclonal EPO Primary Antibody for Neut, WB - ABIN967469
Kitamura, Tange, Terasawa, Chiba, Kuwaki, Miyagawa, Piao, Miyazono, Urabe, Takaku: Establishment and characterization of a unique human cell line that proliferates dependently on GM-CSF, IL-3, or erythropoietin. in Journal of cellular physiology 1989
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Human Polyclonal EPO Primary Antibody for IF (p), IHC (p) - ABIN679718
DeNiro, Al-Mohanna: Nuclear factor kappa-B signaling is integral to ocular neovascularization in ischemia-independent microenvironment. in PLoS ONE 2014
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Human Polyclonal EPO Primary Antibody for ELISA, WB - ABIN153425
Ryou, Choudhury, Li, Winters, Yuan, Liu, Yang: Methylene blue-induced neuronal protective mechanism against hypoxia-reoxygenation stress. in Neuroscience 2015
Human Monoclonal EPO Primary Antibody for WB - ABIN2473499
Gladun: [Theoretical problems of legal regulations of the reorganization of public health in the USSR]. in Sovetskoe zdravookhranenie / Ministerstvo zdravookhranenii?a SSSR 1991
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Human Monoclonal EPO Primary Antibody for ELISA, WB - ABIN515362
Wang, Dou, Lü, Liu: Immuno-magnetic beads-based extraction-capillary zone electrophoresis-deep UV laser-induced fluorescence analysis of erythropoietin. in Journal of chromatography. A 2012
Human Monoclonal EPO Primary Antibody for ICC, ELISA - ABIN969109
Hirschler-Laszkiewicz, Tong, Conrad, Zhang, Flint, Barber, Barber, Cheung, Miller: TRPC3 activation by erythropoietin is modulated by TRPC6. in The Journal of biological chemistry 2009
Data show that erythropoietin (EPO) mRNA was upregulated in the lung, from the metamorphic climax (stage 60) onward.
Fetal plasma EPO concentrations are selectively increased in monochorionic twin pregnancies with intrauterine growth restriction.
SYK (show SYK Antibodies) mediates the actions of EPO and GM-CSF (show CSF2 Antibodies) and coordinates with TGF-beta (show TGFB1 Antibodies) in erythropoiesis.
this study shows that EPO is involved in the pathogenesis of sepsis-induced acute kidney injury
Erythropoietin is superior to the standard prognostic scores in predicting 28-day mortality in patients with acute-on-chronic liver failure.
EPO levels were also found correlated positively with heme, TNF-alpha (show TNF Antibodies), IL-10 (show IL10 Antibodies), IP-10 (show CXCL10 Antibodies) and MCP-1 (show CCL2 Antibodies) during cerebral malaria.
CK1delta enhances EPO secretion from liver cancer cells under hypoxia by modifying HIF-2alpha (show EPAS1 Antibodies) and promoting its nuclear accumulation.
Three single nucleotide polymorphisms are associated with increased risk of diabetic retinopathy in a Chinese Han population.
Pharmacokinetic animal studies revealed strongly 15.6-fold plasma half-life extension for the PASylated EPO (83.16 +/- 13.28 h) in comparison to epoetin alpha (8.5 +/- 2.4 h) and darbepoetin alpha (25.3 +/- 2.2h).
Secreted MIR122 reached the kidney and reduced expression of erythropoietin, contributing to inflammation-induced anemia.
this paper shows that Epo could directly down-regulate pro-inflammatory T cell responses without affecting T cell activation status
EPO expression in myoblasts and myotubes is increased by hypoxia and exercise
these findings define a cis (show CISH Antibodies)-regulatory enhancer network for Epo signaling during erythropoiesis, and provide the framework for future studies involving the interplay of epigenetics and Epo signaling.
FOXD1 (show FOXD1 Antibodies) lineage renal interstitial cells consist of distinct subpopulations that differ in their responsiveness to Phd2 (show EGLN1 Antibodies) inactivation and thus regulation of HIF-2 activity and EPO production under hypoxia or conditions of pharmacologic or genetic PHD (show PDC Antibodies) inactivation.
This study suggests a possible role of EPO in embryonic endodermal development and a new agent for directing the differentiation into endodermal lineages like pancreatic beta-cells.
Smad1 (show SMAD1 Antibodies) and Smad5 (show SMAD5 Antibodies) have overlapping functions to govern hepcidin (show HAMP Antibodies) transcription. Moreover, erythropoietin and erythroferrone target Smad1 (show SMAD1 Antibodies)/5 signaling and require Smad1 (show SMAD1 Antibodies)/5 to suppress hepcidin (show HAMP Antibodies) expression.
EPO role in the glucose homeostasis, thermogenesis and endocrine function of classical brown adipose tissue
Epo transcription in brain pericytes was HIF-2 dependent and cocontrolled by PHD2 (show EGLN1 Antibodies) and PHD3 (show EGLN3 Antibodies), oxygen- and 2-oxoglutarate-dependent prolyl-4-hydroxylases that regulate HIF activity.
This study showed that polycythemia alone and increased levels of plasma Epo blunt the hypercapnic ventilatory response (HCVR); mice with an augmented level of cerebral Epo also had a decreased HCVR.
Epo gene regulation in EPO-producing cells is a complex process that utilizes multiple regulatory influences.
this study shows that EPO could directly promote tumor progression via EPO receptor-expressing macrophages
EPO might play a role as a survival factor or as a mitogen in developing cartilage tissue.
Pyruvate-fortified cardioplegia evokes myocardial erythropoietin signaling in swine undergoing cardiopulmonary bypass.
A single intramuscular injection of recombinant adeno (show ADORA2A Antibodies)-associated virus carrying mutant Epo (R76E) preserves retinal ganglion cells and visual function in glaucomatous mice.
The zebrafish epo cDNA was cloned and the expression of zepo mRNA was mainly in the heart and liver.
characterization of zebrafish epo and epor (show EPOR Antibodies) demonstrates the conservation of an ancient program that ensures proper red blood cell numbers during normal homeostasis and under hypoxic conditions
This gene is a member of the EPO/TPO family and encodes a secreted, glycosylated cytokine composed of four alpha helical bundles. The protein is found in the plasma and regulates red cell production by promoting erythroid differentiation and initiating hemoglobin synthesis. This protein also has neuroprotective activity against a variety of potential brain injuries and antiapoptotic functions in several tissue types.