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NOX4 encodes a member of the NOX-family of enzymes that functions as the catalytic subunit the NADPH oxidase complex. Additionally we are shipping NADPH Oxidase 4 Kits (16) and NADPH Oxidase 4 Proteins (9) and many more products for this protein.
Showing 10 out of 139 products:
Cow (Bovine) Polyclonal NOX4 Primary Antibody for ICC, IHC (fro) - ABIN189715
Maranchie, Zhan: Nox4 is critical for hypoxia-inducible factor 2-alpha transcriptional activity in von Hippel-Lindau-deficient renal cell carcinoma. in Cancer research 2005
Show all 38 references for ABIN189715
Human Polyclonal NOX4 Primary Antibody for IHC (p), WB - ABIN657946
Manea, Tanase, Raicu, Simionescu: Transcriptional regulation of NADPH oxidase isoforms, Nox1 and Nox4, by nuclear factor-kappaB in human aortic smooth muscle cells. in Biochemical and biophysical research communications 2010
Show all 3 references for ABIN657946
Human Polyclonal NOX4 Primary Antibody for FACS, ICC - ABIN258606
Basuroy, Bhattacharya, Leffler, Parfenova: Nox4 NADPH oxidase mediates oxidative stress and apoptosis caused by TNF-alpha in cerebral vascular endothelial cells. in American journal of physiology. Cell physiology 2009
Show all 2 references for ABIN258606
Mouse (Murine) Polyclonal NOX4 Primary Antibody for IHC, WB - ABIN3023201
Wingler, Wünsch, Kreutz, Rothermund, Paul, Schmidt: Upregulation of the vascular NAD(P)H-oxidase isoforms Nox1 and Nox4 by the renin-angiotensin system in vitro and in vivo. in Free radical biology & medicine 2001
Dog (Canine) Polyclonal NOX4 Primary Antibody for IF (p), IHC (p) - ABIN737526
Khan, Byer, Khan: Exposure of Madin-Darby canine kidney (MDCK) cells to oxalate and calcium oxalate crystals activates nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase. in Urology 2014
Data suggest that NOX4 and mitochondrial oxidative stress are mediators of cardiovascular disease in aging under hyperlipidemic conditions.
Downregulation of smooth muscle Nox4 inhibits neointimal hyperplasia by suppressing TSP1 (show THBS1 Antibodies).
High expression of NOX4 is associated with metastasis in prostate cancer.
The angiogenic effect of TRAIL on human microvascular endothelial cell-1 cells i (show NOS3 Antibodies)s downstream of fibroblast growth factor-2, involving NOX4 and nitric oxide signaling.
A deep understanding of Nox4 structure/function and mechanisms of regulation could lead both to the identification of new therapeutic targets and to the development of innovative strategies for appropriate osteoarthritis treatment. [review]
Expression of NOX4/p22(phox (show CYBA Antibodies)) as well as ROS (show ROS1 Antibodies) production is enhanced by IL-1beta (show IL1B Antibodies). On the other hand, the use of NOX4 inhibitors decreased IL-1beta (show IL1B Antibodies)-induced collagenase synthesis by chondrocytes.
Nox4 is a positive transcriptional regulator of cystathionine-gamma-lyase (show CTH Antibodies) in endothelial cells.
An endogenous NOX4 forms macromolecular complexes with calnexin (show CANX Antibodies), which are needed for the proper maturation, processing, and function of NOX4 in the endoplasmic reticulum.
IFNgamma induces oxidative stress, DNA damage and tumor cell senescence via TGFbeta/SMAD signaling-dependent induction of Nox4 and suppression of ANT2
Nox4 knockout (Nox4(-/-)) murine hematopoietic progenitor cells were refractory to FLT3ITD-mediated transformation in vitro
Peroxide derived from superoxide generated by Nox4 appears to maintain a basal relaxation in bovine pulmonary arteries under normoxic conditions, which is removed under hypoxia leading to hypoxic pulmonary vasoconstriction.
proteasome inhibition completely prevented endoplasmic reticulum stress-induced increase in NADPH oxidase (show NOX1 Antibodies) activity, as well as increases in Nox4 isoform and protein disulfide isomerase (show P4HB Antibodies) mRNA expression
the reduction of ROS (show ROS1 Antibodies) generation and NOX4 expression by EA preconditioning might be involved in BBB (show ALMS1 Antibodies) recovery. Therefore, EA may serve as a potential preventive strategy for patients at high risk of ischemic stroke.
Deleterious effect of Nox4 expression in podocytes by promoting podocytopathy in association with albuminuria and extracellular matrix accumulation in experimental diabetes, emphasizes the role of NOX4 as a target for new renoprotective agents.
Downregulation of smooth muscle Nox4 inhibits neointimal hyperplasia by suppressing TSP1 (show GZMA Antibodies).
TRAIL can promote angiogenesis following hindlimb ischemia in vivo via NOX4/eNOS (show NOS3 Antibodies)/nitric oxide signaling.
NOX4 may thus associate with mitochondrial complex I proteins, but in cardiac and renal mitochondria under basal conditions, expression is beyond our detection limits.
These results indicate that Ang-II (show AGT Antibodies) induces cardiac fibroblast proliferation and migration in part via Nox4/ROS (show ROS1 Antibodies)-dependent IL-18 (show IL18 Antibodies) induction and MMP9 (show MMP9 Antibodies) activation, and may involve AT1 (show SLC33A1 Antibodies)/Nox4 physical association.
H2O2-forming NOX4, unlike the superoxide-forming NOX1 (show NOX1 Antibodies), can act as a negative modulator of inflammation and remodeling and convey atheroprotection.
activated PKCzeta (show PRKCZ Antibodies) phosphorylated p65 (show NFkBP65 Antibodies) rel, which led to increased Nox4 synthesis
MRTF down-regulation/inhibition suppresses TGFbeta (show TGFB1 Antibodies)/contact disruption-provoked Nox4 protein and mRNA expression, Nox4 promoter activation, and reactive oxygen species production.
Nox4 NADPH oxidase (show NOX1 Antibodies) mediates oxidative stress and apoptosis caused by TNF-alpha (show TNF Antibodies) in cerebral vascular endothelial cells.
Nox4 NADPH oxidase (show NOX1 Antibodies)-derived reactive oxygen species also initiate a cell survival mechanism by increasing production of carbon monoxide by constitutive heme oxygenase-2 (show HMOX2 Antibodies).
This gene encodes a member of the NOX-family of enzymes that functions as the catalytic subunit the NADPH oxidase complex. The encoded protein is localized to non-phagocytic cells where it acts as an oxygen sensor and catalyzes the reduction of molecular oxygen to various reactive oxygen species (ROS). The ROS generated by this protein have been implicated in numerous biological functions including signal transduction, cell differentiation and tumor cell growth. A pseudogene has been identified on the other arm of chromosome 11. Alternative splicing results in multiple transcript variants.
NADPH oxidase 4
, predicted NADPH oxidase-4
, kidney oxidase-1
, kidney superoxide-producing NADPH oxidase
, renal NAD(P)H-oxidase
, superoxide-generating NADPH oxidase 4