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抗Human EPO 抗体:
抗Rat (Rattus) EPO 抗体:
抗Mouse (Murine) EPO 抗体:
Human Polyclonal EPO Primary Antibody for EIA, WB - ABIN952117
Kristensen, Pedersen-Bjergaard, Schalkwijk, Olsen, Thorsteinsson: Erythropoietin and vascular endothelial growth factor as risk markers for severe hypoglycaemia in type 1 diabetes. in European journal of endocrinology / European Federation of Endocrine Societies 2010
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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 EIA, Func - ABIN112633
Kessler: Rapid isolation of antigens from cells with a staphylococcal protein A-antibody adsorbent: parameters of the interaction of antibody-antigen complexes with protein A. in Journal of immunology (Baltimore, Md. : 1950) 1976
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Human Monoclonal EPO Primary Antibody for WB - ABIN111894
Sue, Sytkowski: Site-specific antibodies to human erythropoietin directed toward the NH2-terminal region. in Proceedings of the National Academy of Sciences of the United States of America 1983
Show all 2 references for ABIN111894
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
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
Data show that erythropoietin (EPO) mRNA was upregulated in the lung, from the metamorphic climax (stage 60) onward.
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
findings suggest that erythropoietin levels in anemia of unknown etiology, although elevated, remain inappropriately low, particularly when compared with other forms of anemia. This suggests a relative erythropoietin deficiency or a blunted erythroid cell response.
Plasma IGFBP-1 (显示 IGFBPI 抗体) was significantly associated with plasma EPO concentration in acute kidney injury, suggesting an unknown mechanism related to systemic stress conditions for EPO regulation in AKI.
Our results suggest that EPO/EPOR (显示 EPOR 抗体) pathway promotes gastric cancer formation, proliferation, migration, and decreases apoptosis
These results suggest that both EpoR (显示 EPOR 抗体)-positive and EpoR (显示 EPOR 抗体)-negative cancer cells could be regulated by exogenous Epo. However, an increased response to erythropoietin was observed in the EpoR (显示 EPOR 抗体)-positive cells. Thus, erythropoietin increases the risk of tumor progression in colon cancer and should not be used to treat anemia in this type of cancer.
Overexpression of EPO is associated with clear cell renal cell carcinoma (显示 MOK 抗体).
EPO may play an important role in stem cell mobilization through up regulating HGF (显示 HGF 抗体) in mesenchymal stem cells and inducing migration of hematopoietic stem/progenitor cells
A review of contemporary aspects of EPO relating to chronic liver disease. [review]
Hepatic EPO synthesis is not enhanced in cirrhosis.
In mice, inflammation increases blood levels of MIR122, which reduces expression of Epo in the kidney.
findings reveal a novel function of LRRK2 (显示 LRRK2 抗体) in regulating EPO expression and imply a potentially novel relationship between PD genes and hematopoiesis.
PI3K, MAPK/ERK (显示 MAPK1 抗体) 1 (显示 MAPK3 抗体)/2, and p38 (显示 CRK 抗体)-signaling proteins are not the main regulators of local production of erythropoietin after 30% loss of circulating blood volume.
The here presented data unearthed EPO-dependent erythroferrone expression acts as an erythropoiesis-driven regulator of iron metabolism under phenylhydrazine-induced hemolytic anemia.
genetic analysis suggests that tubulointerstitial cellular crosstalk modulates renal EPO production under conditions of epithelial HIF activation in the kidney.
DNA methyltransferase (显示 DNMT1 抗体) inhibition restores erythropoietin production in fibrotic murine kidneys
Midazolam suppresses hypoxia-induced up-regulation of EPO in brain.
erythropoietin activates AKT (显示 AKT1 抗体), which phosphorylates GATA-1 (显示 GATA1 抗体) at Ser310, thereby increasing GATA-1 (显示 GATA1 抗体) affinity for FOG-1 (显示 ZFPM1 抗体)
a novel RIPC mechanism in which inhibition of infarct size by RIPC is produced through the renal nerve-mediated reduction of RBF (显示 ATP5I 抗体) associated with activation of the HIF1alpha (显示 HIF1A 抗体)-EPO pathway.
Our data suggest that EPO-alpha and EPO-Z are not biosimilars for the wound healing effects. The higher efficacy of EPO-alpha might be likely due to its different conformational structure leading to a more efficient cell proliferation and skin remodelling.
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 (显示 ADORA2A 抗体)-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 (显示 EPOR 抗体) 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.