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SIRT3 encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Zusätzlich bieten wir Ihnen SIRT3 Kits (26) und SIRT3 Proteine (14) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 235 products:
Human Polyclonal SIRT3 Primary Antibody für IHC (p), WB - ABIN390178
Pillai, Sundaresan, Kim, Gupta, Rajamohan, Pillai, Samant, Ravindra, Isbatan, Gupta: Exogenous NAD blocks cardiac hypertrophic response via activation of the SIRT3-LKB1-AMP-activated kinase pathway. in The Journal of biological chemistry 2010
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Cow (Bovine) Polyclonal SIRT3 Primary Antibody für IHC, WB - ABIN2779610
Onyango, Celic, McCaffery, Boeke, Feinberg: SIRT3, a human SIR2 homologue, is an NAD-dependent deacetylase localized to mitochondria. in Proceedings of the National Academy of Sciences of the United States of America 2002
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Hamster Polyclonal SIRT3 Primary Antibody für IHC (p), WB - ABIN652184
Kawamura, Uchijima, Horike, Tonami, Nishiyama, Amano, Asano, Kurihara, Kurihara: Sirt3 protects in vitro-fertilized mouse preimplantation embryos against oxidative stress-induced p53-mediated developmental arrest. in The Journal of clinical investigation 2010
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Human Polyclonal SIRT3 Primary Antibody für ELISA, WB - ABIN269822
Shi, Wang, Stieren, Tong: SIRT3, a mitochondrial sirtuin deacetylase, regulates mitochondrial function and thermogenesis in brown adipocytes. in The Journal of biological chemistry 2005
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Results show that curcumin at low doses can increase the level of sirtuins including sirtuin 1 (zeige SIRT1 Antikörper) and sirtuin 3) without delaying senescence of vascular smooth muscle (VSMC) cells.
survival curves showed that higher SIRT3 expression is correlated to a poorer prognosis for patients with grade 3 breast cancer. In conclusion, SIRT3 could be a therapeutic target for breast cancer, improving the effectiveness of CDDP and TAM (zeige CCNA1 Antikörper) treatments.
There were no significant correlations between LRP130 (zeige LRPPRC Antikörper), SIRT3, or PGC-1alpha (zeige PPARGC1A Antikörper) mRNA expression in response to acute sprint-interval training. Changes in protein expression of LRP130 (zeige LRPPRC Antikörper), SIRT3, and PGC-1alpha (zeige PPARGC1A Antikörper) were positively correlated at several time points with large effect sizes, which suggest that the regulation of these proteins may be coordinated in human skeletal muscle.
In human myometrium, SIRT3 expression decreases with term labor and regulates the mediators involved in the terminal effector pathways of human labor and delivery through the NFkappaB1 pathway.
Mitochondria-targeted esculetin has anti-atherosclerotic effects by inhibiting PAI-1 (zeige SERPINE1 Antikörper) levels by modulating miR (zeige MLXIP Antikörper)-19b and -30c expression and affecting SIRT3- and STAT3 (zeige STAT3 Antikörper)-mediated signaling pathways.
the activation of the SIRT3 axis of the UPRmt is linked to metastasis.
these results suggest a potential relationship between SIRT3 enzymatic activity, IDH2 (zeige IDH2 Antikörper)-K413 acetylation-determined dimerization, and a cancer-permissive phenotype
These data suggest a novel role for SIRT3 deficiency in mediating alveolar epithelial cell mtDNA damage, apoptosis, and lung fibrosis.-
Data suggested a protective role of the SIRT3 single-nucleotide polymorphism rs4980329 in ALS risk.
Low SIRT3 expression is associated with metastasis and epithelial-mesenchymal transition in hepatocellular carcinoma.
Sirtuin 3 is required for osteogenic differentiation through maintenance of PGC (zeige PGC Antikörper)-1a-SOD2 (zeige SOD2 Antikörper)-mediated regulation of mitochondrial function
findings reveal an unexpected mechanism for SIRT3 regulation via SIRT1 (zeige SIRT1 Antikörper)-mediated deacetylation. Improving mitochondrial SIRT3 functions by inhibiting SIRT3 acetylation may offer a new therapeutic approach for obesity- and aging-related diseases associated with mitochondrial dysfunction.
Sirt3 expression in bone marrow cells increases during aging, suggesting that Sirt3 promotes age-related adipogenesis and osteoclastogenesis associated with bone loss. These findings identify Sirt3 as an important regulator of adipogenesis and skeletal homeostasis in vivo and identify Sirt3 as a potential target for the treatment of osteoporosis.
Diminished Sirt3 expression and redox inactivation of Sirt3 led to SOD2 (zeige SOD2 Antikörper) inactivation and contributes to hypertension.
Data suggest that negative regulatory effect of Sirt3 on Nlrp3 (zeige NLRP3 Antikörper) inflammasome assembly in macrophages due to prolonged fasting occurs via Sirt3-mediated deacetylation of mitochondrial Sod2 (zeige SOD2 Antikörper), leading to Sod2 (zeige SOD2 Antikörper) activation; prolonged fasting blunts inflammasomes in wild-type mice but not in Sirt3 knock-out mice. (Sirt3 = sirtuin 3; Nlrp3 (zeige NLRP3 Antikörper) = NLR (zeige CXCR5 Antikörper) family, pyrin domain containing 3 protein; Sod2 (zeige SOD2 Antikörper) = superoxide dismutase 2 (zeige SOD2 Antikörper))
Results reveal a potential mechanism by which SIRT3 deletion exacerbates post-MI cardiac dysfunction and impairment of cardiac recovery involving microvascular rarefaction and pre-existing coronary microvascular dysfunction.
expression and activity of the NADase CD38 increase with aging and that CD38 is required for the age-related NAD decline and mitochondrial dysfunction via a pathway mediated at least in part by regulation of SIRT3 activity.
Data show that resveratrol reduced mitochondrial reactive oxygen species (mROS) generation by promoting Sirt3 enrichment within the mitochondria and subsequent upregulation of FoxO3a (zeige FOXO3 Antikörper)-mediated mitochondria gene expression of PGC-1alpha (zeige PPARGC1A Antikörper) and SOD2 (zeige SOD2 Antikörper).
These data demonstrate a critical role of SIRT3 in the control of myofibroblast differentiation and lung fibrosis.
The results indicate that the polymorphisms in transcription factor binding sites of SIRT3 promoter may affect the transcriptional activity of SIRT3, and thus alter intramuscular fat content in beef cattle.
The results indicate that the variations in the class I sirtuin (zeige SIRT1 Antikörper) genes and their corresponding genotypes may be considered as molecular markers for economic traits in cattle breeding.
The expression profile of sirtuin 1 (zeige SIRT1 Antikörper) and sirtuin 3 in the liver, muscle, and adipose tissue of calves and bulls is reported.
This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined\; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Two alternatively spliced transcript variants that encode different proteins have been described for this gene.
, NAD-dependent deacetylase sirtuin-3, mitochondrial
, NAD-dependent protein deacetylase sirtuin-3, mitochondrial
, SIR2-like protein 3
, mitochondrial nicotinamide adenine dinucleotide-dependent deacetylase
, regulatory protein SIR2 homolog 3
, silent mating type information regulation 2, S.cerevisiae, homolog 3
, sir2-like 3
, sirtuin type 3
, SIRT3 mitochondrial
, NAD-dependent deacetylase sirtuin-3
, NAD-dependent protein deacetylase sirtuin-3
, SIRT3L mitochondrial
, mitochondrial protein lysine deacetylase
, silent mating type information regulation 2, (S.cerevisiae, homolog)-like 3