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Canalicular ectonucleoside NTPDase responsible for the main hepatic NTPDase activity. Zusätzlich bieten wir Ihnen Ectonucleoside Triphosphate diphosphohydrolase 1 Kits (17) und Ectonucleoside Triphosphate diphosphohydrolase 1 Proteine (17) und viele weitere Produktgruppen zu diesem Protein an.
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Horse (Equine) Polyclonal ENTPD1 Primary Antibody für ICC, IF - ABIN4292709
Hayes, Cairns, Levashova, Chinn, Perez, Theunissen, Liao-Chan, Bermudez, Flory, Schweighofer, H van der Horst: CD39 is a promising therapeutic antibody target for the treatment of soft tissue sarcoma. in American journal of translational research 2015
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Human Monoclonal ENTPD1 Primary Antibody für FACS, IP - ABIN610072
Estival, Monzat, Miquel, Gaubert, Hollande, Korc, Vaysse, Clemente: Differential regulation of fibroblast growth factor (FGF) receptor-1 mRNA and protein by two molecular forms of basic FGF. Modulation of FGFR-1 mRNA stability. in The Journal of biological chemistry 1996
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Human Monoclonal ENTPD1 Primary Antibody für FACS, IP - ABIN610073
Fox, Shanley: Antisense inhibition of basic fibroblast growth factor induces apoptosis in vascular smooth muscle cells. in The Journal of biological chemistry 1996
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Mouse (Murine) Monoclonal ENTPD1 Primary Antibody für FACS - ABIN2480163
Dwyer, Deaglio, Gao, Friedman, Strom, Robson: CD39 and control of cellular immune responses. in Purinergic signalling 2008
Human Monoclonal ENTPD1 Primary Antibody für - ABIN786711
Dahlenborg, Pound, Gordon, Borrebaeck, Carlsson: Signals sustaining human immunoglobulin V gene hypermutation in isolated germinal centre B cells. in Immunology 2000
Mouse (Murine) Polyclonal ENTPD1 Primary Antibody für CyTOF, FACS - ABIN4900311
De Giorgi, Enjyoji, Jiang, Csizmadia, Mitsuhashi, Gumina, Smolenski, Robson: Complete deletion of Cd39 is atheroprotective in apolipoprotein E-deficient mice. in Journal of lipid research 2018
Mouse (Murine) Monoclonal ENTPD1 Primary Antibody für CyTOF, FACS - ABIN4900313
Yu, Robson, Hill: Expression and distribution of ectonucleotidases in mouse urinary bladder. in PLoS ONE 2011
Extracellular ATP hydrolysis via NTPDase1 action inhibits synaptic transmission by pannexin 1 (zeige PANX1 Antikörper)-mediated increase in pH buffering of the synaptic cleft.
CD39 expression and activity is attenuated in lung tissue of chronic obstructive pulmonary disease patients.
monocyte-derived macrophages from ankylosing spondylitis patients expressed reduced levels of CD39 mRNA compared to those from healthy controls
ur results demonstrate that CD39 is upregulated on conventional CD4 (zeige CD4 Antikörper)+ and CD8 (zeige CD8A Antikörper)+ T cells at sites of acute infection and inflammation, and that CD39 dampens responses to bacterial infection.
this paper shows that simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro
The peripheral blood mononuclear cells (PBMC) from the transgenic pigs were more resistant to lysis by pooled complement-preserved normal human serum than that from wild type (WT) pig. Accordingly, GGTA1 mutated piglets expressing hCD39 will provide a new organ source for xenotransplantation research
Phosphoantigens (pAgs) induced expression of the ecto-ATPase CD39, which, however, not only hydrolyzed ATP but also abrogated the gammadelta T cell receptor (TCR) agonistic activity of self and microbial pAgs.
These studies showed that the G allele of rs3176891 marks a haplotype associated with increased clotting and platelet aggregation attributable to a promoter variant associated with increased transcription, expression, and activity of NTPDase1.
Transgenic expression of human CD39 is associated with increased renal fibrosis after ischemia in mice.
CD39 overexpression protects against cerebral ischemia in a transgenic mouse model.
Ablation of CD73 minimally effects in vivo thrombosis, but increased CD39 expression on hematopoietic-derived cells, especially monocytes, attenuates in vivo arterial thrombosis.
CD39 is highly expressed by CD8 (zeige CD8A Antikörper)+ tumor-infiltrating T lymphocytes.
Furthermore, our results suggest a crucial role for the enzyme CD39 in limiting P2X7 receptor (zeige P2RX7 Antikörper) proinflammatory responses since CD39(-/-) septic mice exhibited higher levels of IL-1beta (zeige IL1B Antikörper) in the brain.
CD39 expression in macrophages limits P2X7 (zeige P2RX7 Antikörper)-mediated pro-inflammatory responses, scavenging extracellular ATP and ultimately generating adenosine. CD39 genetic deletion exacerbates sepsis-induced experimental liver injury.
complete deletion of Cd39 paradoxically attenuates development of atherosclerosis in hyperlipidemic mice
Deletion of CD39 and CD73 or both caused an inhibition of the microglia ramified phenotype in the brain with a reduction in the length of processes, branching frequency and number of intersections with Sholl spheres. In vitro, unlike wild-type microglia, cd39-/- and cd73-/- microglial cells were less complex and did not respond to ATP with the transformation into a more ramified phenotype.
CD39 expression by Th17 cells allows the depletion of ATP and is crucial for IL-10 (zeige IL10 Antikörper) production and survival during the resolution of intestinal inflammation.
Cardiac-specific expression of CD39 reduces myocardial dysfunction and infarct size following ischemia-reperfusion injury
Data indicate that adenosine and CGS21680 upregulate CD39 and CD73 via E2F-1 (zeige E2F1 Antikörper) and CREB (zeige CREB1 Antikörper).
Acute cigarette smoke exposure induced CD39 upregulation in murine lungs and BALF cells. CD39 inhibition and deficiency led to augmented lung inflammation.
T Lymphocyte Inhibition by Tumor-Infiltrating Dendritic Cells Involves Ectonucleotidase CD39 but Not Arginase-1 (zeige ARG1 Antikörper).
CD39 and CD73 and their enzymatic activities that convert extracellular nucleotides are highly expressed and could have special function in the valve
Canalicular ectonucleoside NTPDase responsible for the main hepatic NTPDase activity. Ectonucleoside ATPases catalyze the hydrolysis of gamma- and beta-phosphate residues of nucleotides, playing a central role in concentration of extracellular nucleotides.
, NTPDase 1
, ecto-ATP diphosphohydrolase 1
, ecto-ATPDase 1
, ecto-ATPase 1
, lymphoid cell activation antigen
, ectonucleoside triphosphate diphosphohydrolase 1