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Here we demonstrate that the Drosophila relaxin (zeige 0 Antikörper) receptor homolog Lgr3 (zeige TSHR Antikörper), a leucine-rich repeat-containing G-protein-coupled receptor (zeige GPBAR1 Antikörper), is required for Dilp8-dependent growth coordination and developmental delay during the regeneration checkpoint; we demonstrate that Lgr3 (zeige TSHR Antikörper) activity in both the CNS and PG is necessary for NOS activation in the PG following damage
Nitric Oxide Synthase Regulates Growth Coordination During Drosophila melanogaster Imaginal Disc Regeneration
Hb9 (zeige MNX1 Antikörper) governs neuronal specification and differentiation and activates expression of Nos and fd59a in the Drosophila CNS
Nitric oxide synthase is not essential for Drosophila development.
biochemical characterization of Drosophila nitric oxide synthase
Oxygenase domain of Drosophila melanogaster Nos: unique kinetic parameters enable a more efficient NO release.
Reductase domain of Drosophila melanogaster Nos: redox transformations, regulation, and similarity to mamalian homologues.
These data suggest that BmNOS has an important role in the early embryonic development of the B. mori.
ur findings endorse polymorphic regulation of iNOS (zeige NOS2 Antikörper) expression, altered oxidant-antioxidant components and evidences of risk association as the hallmark of malaria pathogenesis. iNOS (zeige NOS2 Antikörper)/NO may serve as potential diagnostic marker in assessing clinical malaria.
The results indicated that the expression levels of interleukin6 and inducible nitric oxide synthase (iNOS (zeige NOS2 Antikörper)) were decreased, whereas collagen expression and deposition were increased in ketaminetreated SMCs. Conversely, treatment with CTX (zeige CYP27A1 Antikörper) restored the expression of iNOS (zeige NOS2 Antikörper), which may prevent or limit oxidative damage
The present study demonstrated that iNOS (zeige NOS2 Antikörper) C150T polymorphism did not show significant association with metabolic syndrome.
KLF4 (zeige KLF4 Antikörper) activated the transcription activity of iNOS (zeige NOS2 Antikörper) promoter in MH7A cells stimulated by TNF-alpha (zeige TNF Antikörper). This study indicates that KLF4 (zeige KLF4 Antikörper) is important for regulating the expression of iNOS (zeige NOS2 Antikörper) by TNF-alpha (zeige TNF Antikörper) in human synoviocytes.
Coexpression of NOS2 and COX2 (zeige COX2 Antikörper) accelerates tumor growth and reduces survival in estrogen receptor (zeige ESR1 Antikörper)-negative breast cancer.
NOS2 T allele of rs2297514 significantly increased the risk of a non-union during the fracture healing process by 38% compared to the C allele. Further stratification analyses conducted for this SNP using data from subgroups classified by different sites of fracture indicated that significance could only be observed in the tibial diaphysis subgroup.
NOS2 polymorphisms in prediction of benefit from first-line chemotherapy in metastatic colorectal cancer patients
PEDF (zeige SERPINF1 Antikörper) protects human glomerular mesangial cells from diabetes-derived oxidative stress via NOXO1 (zeige NOXO1 Antikörper)- iNOS (zeige NOS2 Antikörper) suppression.
The studies established a potential link between leptin and adipocyte insulin responsiveness in an NOS2 dependent manner.
Collectively, our results demonstrated sanggenon C induced apoptosis of colon cancer cells by increased reactive oxygen species generation and decreased nitric oxide production, which is associated with inhibition of inducible nitric oxide synthase (zeige NOS2 Antikörper) expression(iNOS (zeige NOS2 Antikörper)) and activation of mitochondrial apoptosis pathway.
Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase which is expressed in liver and is inducible by a combination of lipopolysaccharide and certain cytokines. Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17.
, NO synthase
, nitric oixide synthase
, nitric oxide synthase
, Nitric oxide synthase, brain
, inducible nitric oxide synthase-like protein
, NOS type II
, NOS, type II
, hepatocyte NOS
, inducible NO synthase
, inducible NOS
, nitric oxide synthase 2A (inducible, hepatocytes)
, nitric oxide synthase, inducible
, nitric oxide synthase, macrophage
, peptidyl-cysteine S-nitrosylase NOS2