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Coral Polyclonal SOD1 Primary Antibody für IP, IHC - ABIN361646
Adachi, Ohta, Yamada, Futenma, Kato, Hirano: Quantitative analysis of extracellular-superoxide dismutase in serum and urine by ELISA with monoclonal antibody. in Clinica chimica acta; international journal of clinical chemistry 1993
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Fish Monoclonal SOD1 Primary Antibody für ELISA, FACS - ABIN4355061
Jung, Choi, Kim, Choi, Kim, Choi: Effects of melatonin injection or green-wavelength LED light on the antioxidant system in goldfish (Carassius auratus) during thermal stress. in Fish & shellfish immunology 2016
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Human Monoclonal SOD1 Primary Antibody für WB - ABIN967513
Reaume, Elliott, Hoffman, Kowall, Ferrante, Siwek, Wilcox, Flood, Beal, Brown, Scott, Snider: Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. in Nature genetics 1996
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Cow (Bovine) Polyclonal SOD1 Primary Antibody für ICC, IF - ABIN361652
Gao, Flores, Leff, Bose, McCord: Synthesis and anti-inflammatory activity of a chimeric recombinant superoxide dismutase: SOD2/3. in American journal of physiology. Lung cellular and molecular physiology 2003
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Human Polyclonal SOD1 Primary Antibody für EIA, ELISA - ABIN253166
DeRuisseau, Recca, Mogle, Zoccolillo, DeRuisseau: Metallothionein deficiency leads to soleus muscle contractile dysfunction following acute spinal cord injury in mice. in American journal of physiology. Regulatory, integrative and comparative physiology 2009
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Cow (Bovine) Polyclonal SOD1 Primary Antibody für IHC (p), WB - ABIN4355068
Kumar, Rao, Pal, Pal: Hyperglycemia-induced oxidative stress induces apoptosis by inhibiting PI3-kinase/Akt and ERK1/2 MAPK mediated signaling pathway causing downregulation of 8-oxoG-DNA glycosylase levels in glial cells. in The international journal of biochemistry & cell biology 2014
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Human Polyclonal SOD1 Primary Antibody für IP, IHC - ABIN223175
Kim, Kim, Hwang, Lee, Shin, Gwag, Koh: Accumulation of labile zinc in neurons and astrocytes in the spinal cords of G93A SOD-1 transgenic mice. in Neurobiology of disease 2009
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Chimpanzee Polyclonal SOD1 Primary Antibody für ELISA, WB - ABIN1574003
Rajkumar, Vasavada, Praveen, Ananthan, Reddy, Tripathi, Ganatra, Arora, Patel: Exploration of molecular factors impairing superoxide dismutase isoforms activity in human senile cataractous lenses. in Investigative ophthalmology & visual science 2013
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Human Polyclonal SOD1 Primary Antibody für ICC, IF - ABIN4355064
Filézac de LEtang, Maharjan, Cordeiro Braña, Ruegsegger, Rehmann, Goswami, Roos, Troost, Schneider, Weis, Saxena: Marinesco-Sjögren syndrome protein SIL1 regulates motor neuron subtype-selective ER stress in ALS. in Nature neuroscience 2015
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Human Polyclonal SOD1 Primary Antibody für IP, IHC - ABIN289407
Nakamura, Omaye: Alpha-tocopherol modulates human umbilical vein endothelial cell expression of Cu/Zn superoxide dismutase and catalase and lipid peroxidation. in Nutrition research (New York, N.Y.) 2008
In this newborn mouse lung hypoxia-reoxygenation model, we found downregulation of genes of mediators of inflammation, an antiapoptotic gene expression pattern, and downregulation of DNA glycosylases. Sod1 and Il1b (zeige IL1B Antikörper) were significantly differentially expressed when comparing reoxygenation using 60% O2 with air.
the senescence associated secretory phenotype was also increased significantly in the kidney of Sod1(-/)(-) mice compared to WT mice as measured by the expression of transcripts for IL-6 (zeige IL6 Antikörper) and IL-1b (zeige IL1B Antikörper)
Our study provides the first direct evidence that Abeta, an AD-linked factor, is associated to the pathogenesis of ALS and provides molecular clues to understand common aggregation mechanisms in the pathogenesis of neurodegenerative diseases.
deletion-rescue experiments show that a respiration-defective mutant of SOD1 is also impaired in its ability to rescue cells from toxicity caused by SOD1 deletion
These findings indicate that a loss of Sig1R function is causative for juvenile amyotrophic lateral sclerosis (ALS16), and collapse of the mitochondria-associated membrane is a common pathomechanism in both Sig1R- and SOD1-linked ALS.
the aberrant mutant SOD1-G3BP1 (zeige G3BP1 Antikörper) interaction affects stress granule dynamics
the absence of IP3R2 led to increased innate immunity, which may contribute to the decreased survival of the SOD1(G93A) mice.our data indicate that IP3R2 protects against the negative effects of inflammation, suggesting that the increase in IP3R2 expression in ALS patients is a protective response.
the redox regulation of Jmjd3 (zeige Kdm6b Antikörper) is a unique regulatory mechanism for Cu,Zn-superoxide dismutase-mediated profibrotic macrophage polarization.
two ALS-linked factors, SQSTM1 (zeige SQSTM1 Antikörper) and ALS2 (zeige ALS2 Antikörper), have distinct but additive protective roles against mutant SOD1-mediated toxicity by modulating neuronal proteostasis possibly through the autophagy-endolysosomal system.
we showed that, in the absence of ERalpha (zeige ESR1 Antikörper), G93A-SOD1 failed to activate OMI (zeige HTRA2 Antikörper) and the proteasome, confirming the ERalpha (zeige ESR1 Antikörper) dependence of the response. Taken together, these results demonstrate the IMS-UPRmt activation in SOD1 familial Amyotrophic lateral sclerosis , and suggest that sex differences in the disease phenotype could be linked to differential activation of the ERa axis of the IMS-UPRmt
the C. elegans intracellular CuZn-SODs (wSOD-1 and wSOD-5) are not dependent on the copper chaperone CCS (zeige CCS Antikörper) for activation
although several long-lived mutants of Caenorhabditis elegans have increased SOD levels, this phenomenon does not correlate with life span or growth rate.
SOD isoforms play no role in lifespan in ad lib (zeige LRRC15 Antikörper) or dietary restricted conditions, but mutational inactivation of SOD-1 reduces life extension by cold.
the ALS-linked mutant SOD1 produces a locomotor defect associated with aggregation and synaptic dysfunction when expressed in neurons of Caenorhabditis elegans
this suggests that the activity of SOD-1, which so far has been thought to act mainly in cytoplasm, helps to control the detoxification of *O2- also in the mitochondria.
The functional SOD1 and SOD2 (zeige SOD2 Antikörper) genes knockout and their overexpression in neurons and glial tissue increase the sensitivity of Drosophila melanogaster to oxidative stress conditions.
Expression of zinc-deficient human superoxide dismutase (zeige SOD2 Antikörper) in Drosophila neurons produces a locomotor defect linked to mitochondrial dysfunction.
curcumin increases mean lifespan of Drosophila via regulating gene expression of the key enzyme SOD and reducing accumulation of MDA and lipid peroxidation.
The activity of carbohydrate metabolizing enzymes, lipid and triglyceride concentration, and steady state NADPH:NADP(+) in SOD1-null and control transgenic rescue flies, was analysed.
Overexpression of Cu,ZnSOD and MnSOD (zeige SOD2 Antikörper) in transgenic Drosophila.
Effects of overexpression of copper-zinc and manganese superoxide dismutases, catalase, and thioredoxin reductase genes on longevity.
SOD1 and SOD2 (zeige SOD2 Antikörper) provide independent protection to compartment-specific protein iron-sulfur clusters against attack by superoxide generated under oxidative stress
A 1140 base pair region, composed of the single sod1 intron along with exon 2, was found to be essential for permitting spatial and temporal expression patterns that approximate normal endogenous expression.
Cu/Zn superoxide dismutase has a role in preventing spontaneous DNA damage
Instability of superoxide dismutase 1 of Drosophila in mutants deficient for its cognate copper chaperone
The various biochemical and structure-based hypotheses proposed for mutant SOD1-associated Amyotrophic Lateral Sclerosis are discussed [REVIEW]
Using different methods to detect misfolded SOD1, multiple misfolded SOD1 antibodies raised against different epitopes, appropriate parallel controls and by controlling for staining artefacts through the comparison of different antigen retrieval methods, study demonstrated that misfolded SOD1 is not a contributing component of sporadic amyotrophic lateral sclerosis.
The results show that the docking of the electrostatic loop to the rest of SOD1 plays a role in amyotrophic lateral sclerosis (ALS (zeige IGFALS Antikörper)) pathogenesis, in support of that structure acting as a solvent barrier for the metal site. The results provide a unified pathogenic mechanism for five different ALS (zeige IGFALS Antikörper)-linked mutations of SOD1.
SOD1 is the seeding particle responsible for the spread of SOD1-familial amyotrophic lateral sclerosis neurodegeneration from its initial onset site
The results suggest that SFH prevents the degeneration of pancreatic islets via increasing SOD while hyperglycemia is alleviated by maintaining beta cell mass in type 2 diabetes model mice.
study thus implies that the WT and mutant SOD1 indeed converge on a common mechanism for gain of cytotoxicity by abnormally interacting with membranes. Moreover, any genetic/environmental factors which can delay or impair its maturation might act to transform SOD1 into cytotoxic forms with the acquired capacity to abnormally interact with membranes.
Data suggest that multiple non-native species of misfolded SOD1 may exist in the SOD1(G93A) rat model, some of which are associated with mitochondrial damage, highlighting that variable potency/toxicity of different SOD1 species is possible even when only one SOD1 mutation is present.
SOD1 is one of the most commonly mutated genes in ALS.
superoxide dismutase function of SOD1 might not be required to preserve DNA integrity in motor neurons, at least when the function of TDP-43 (zeige TARDBP Antikörper) is unaltered
The results suggest that the 50 bp deletion has a moderate reducing effect on SOD1 synthesis.
CuZnSOD mRNA is a broad-spectrum expression gene, which was detected in brain, heart, spleen, liver, kidney, lung, large intestine, small intestine, spinal cord, muscle, backfat, and stomach
SOD catalyzes reversal of autoxidation manifesting as its inhibition. SOD saves catechols from autoxidation and extends their bioavailability
antioxidative enzymatic mechanisms in bovine placental tissues are represented by superoxide dismutase 1 and glutathione peroxidase (zeige GPX1 Antikörper), which show the changes in their expression during improper placental release
Results sugget thet Copper/Zinc superoxide dismutase (SOD1) may play a role in controlling intraluteal prostaglandin F2alph and reactive oxygen species action during functional and structural luteolysis.
ALOX5AP (zeige ALOX5AP Antikörper), CPNE3 (zeige CPNE3 Antikörper), IL1R2 (zeige IL1R2 Antikörper), IL6 (zeige IL6 Antikörper), TLR2 (zeige TLR2 Antikörper), TLR4 (zeige TLR4 Antikörper), and THY1 (zeige THY1 Antikörper) were upregulated in blood polymorphonuclear cells in negative energy balance versus positive energy balance cows.
Acute elevation of SOD may represent a response of luteal endothelial cells to protect themselves against oxidative stress induced (zeige SQSTM1 Antikörper) by PGF (zeige PGF Antikörper) during functional luteolysis.
At room temperature (25.0 degrees C) and higher, the addition of high concentrations of polymer is found to significantly enhance the affinity of SOD for catalase (zeige CAT Antikörper).
Capillary electrophoresis and mass spectrometry to study the different structures of bovine SOD-1. In both cases, an average molecular mass corresponding to the apo (zeige C9orf3 Antikörper)-monomer SOD-1 was calculated.
flexibility of the metal sites involved in present a single-crystal X-ray diffraction study of Cu,Zn superoxide dismutase in space group P212121 at 0.57 GPa (zeige GYPA Antikörper). The crystal structure (hpSOD) was determined and refined at 2 A degrees resolution.
expression profile in follicles: oocytes (SOD1 throughout ooplasm (zeige NLRP5 Antikörper) & nucleoplasm); cumulus cells (no SOD1 detected); granulosa cells (expressed SOD1); follicular fluid (small follicles show increased amounts of SOD1 in comparison with large follicles)
Bovine erythrocyte Cu,Zn-superoxide dismutase (BESOD) is a dimeric enzyme composed of identical subunits associated through unusually strong non-covalent interactions.
amyloid and oxidative stress-related disease proteins like SOD 1 is increased in expression and form localized accumulations in diabetic muscle in this rabbit model of diabetes.
fenofibrate almost completely abolished GM-induced reactive oxygen species generation, which seemed to be mediated at least in part by the restoration of the expression of PPARalphadependent antioxidant enzymes, including catalase (zeige CAT Antikörper) and superoxide dismutase (SOD)-1.
The earliest event in the pathophysiology of amyotrohic lateral sclerosis in the mutant sod1 zebrafish model involves neuronal stress in inhibitory interneurons, resulting from mutant Sod1 expression.
A hierarchic gene expression of copper homeostatic genes was demonstrated between atp7a (zeige ATP7A Antikörper), sp1 (zeige SP1 Antikörper) and sod1 in zebrafish.
depresses cathepsin L activity stimulated by free radicals and prevents otic complications associated with bone erosion
Copper/zinc superoxide dismutase was cloned from the zebrafish ( Danio rerio). Evidence is presented that SOD protects against paraquat toxicity in fish.
Glia maturation factor (zeige GMFG Antikörper)-null cells ahow a concurrent decrease in CuZnSOD astrocytes.
The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene.
superoxide dismutase [Cu-Zn]
, Cu/Zn superoxide dismutase
, superoxide dismutase 1 soluble
, superoxide dismutase
, Cu/Zn SOD
, insulin-like growth factor-binding protein complex acid labile subunit
, insulin-like growth factor binding protein complex acid-labile subunit
, insulin-like growth factor-binding protein complex acid labile chain
, Cu, Zn superoxide dismutase
, Cu-Zn superoxide dismutase
, Cu/Zn-Superoxide dismutase
, CuZn superoxide dismutase
, CuZn-superoxide dismutase
, CuZn-superoxide dismutase (SOD)1
, Cu[2+] Zn[2+] superoxide dismutase
, Cu[2+]Zn[2+] superoxide dismutase
, Mn superoxide dismutase
, complementation group G
, copper and zinc SOD
, copper-zinc superoxide
, copper-zinc superoxide dismutase
, cytoplasmic Cu/ZnSOD
, super oxide dismutase
, superoxidase dismutase
, superoxide dismutase 1
, superoxide dismutatase
, superoxido dismutase
, tetrazolium oxidase
, tetrazolium oxidase-1
, SOD, soluble
, indophenoloxidase A
, superoxide dismutase, cystolic
, Cu(2+)-Zn2+ superoxide dismutase
, superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult))
, Cu-Zn-superoxide dismutase
, Cu,Zn-superoxide dismutase
, Cu,Zn superoxide dismutase
, superoxide dismutase [Cu-Zn] B