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a class of opioid receptors; show selective affinity for the endogenous opioid dynorphin. 再加上，我们可以发Opioid Receptor, kappa 1 抗体 (124) 和 Opioid Receptor, kappa 1 蛋白 (3)和数多这个蛋白质的别的产品。
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ZFOR3 is a unique model to study kappa opioid receptor functionality
These findings provide evidence that previously demonstrated KOR-mediated reduction in intraocular pressure could be caused, in part, by NO production in both the ciliary body and the trabecular meshwork.
Functional activity of Dynorphin 1-17 and fragments (1-6, 1-7 and 1-9) were screened over a range of concentrations against forskolin stimulated human embryonic kidney 293 (HEK (显示 EPHA3 ELISA试剂盒)) cells stably transfected with one of KOP (显示 SPINT2 ELISA试剂盒), MOP (显示 NLN ELISA试剂盒) or DOP (显示 COPB2 ELISA试剂盒)
These results indicate that KOR can form a heterodimer with B2R (显示 BDKRB2 ELISA试剂盒) and this leads to increased protein kinase A activity by the CREB (显示 CREB1 ELISA试剂盒) signaling pathway, leading to a significant increase in cell proliferation.
that promoter fragments of OPRK1 and OPRM1 (显示 OPRM1 ELISA试剂盒) were able to upregulate gene expression with mild cognitive impairment
Heterodimerization of the kappa opioid receptor and neurotensin receptor 1 contributes to a novel beta-arrestin-2 (显示 ARRB2 ELISA试剂盒)-signaling pathway.
Hypoxia inducible factor-1alpha (HIF-1alpha (显示 HIF1A ELISA试剂盒)) siRNA knocked down the increase of endogenous HIF-1alpha (显示 HIF1A ELISA试剂盒) messages and diminished the desferrioxamine (DFO)-induced increase of kappa-opioid receptor (hKOR) expression.
genetic association studies in a population in Denmark: Data suggest that carriers/heterozygotes of the C allele (CC/CT) of OPRK SNP rs6473799 report a 30.4% higher mechanical visceral pain tolerance threshold than non-carriers.
Molecular switches of the kappa opioid receptor triggered by 6'-GNTI (显示 MGAT1 ELISA试剂盒) and 5'-GNTI (显示 MGAT1 ELISA试剂盒) have been described.
The study successfully developed a population PKPD model for oxycodone across three experimental pain types and investigated the association between 18 SNPs across all three opioid receptor genes (OPRM1 (显示 OPRM1 ELISA试剂盒), OPRK1, OPRD1 (显示 OPRD1 ELISA试剂盒)) and analgesic response from oxycodone. None of the selected polymorphisms were significantly associated with analgesic response of oxycodone.
findings suggest that SNPs in opioid receptors and the PNOC (显示 PNOC ELISA试剂盒) genes are associated with NAS (显示 SCN9A ELISA试剂盒) severity.
OPRK1 promoter hypermethylation might increase the risk of AD through its regulation on the gene expression of OPRK1.
The kappa opioid receptor was identified as a key player mediating the effects of buprenorphine in tests sensitive to antidepressant drugs in mice.
This study provides the first evidence for a time- and learning-dependent property of neocortical kappa opioid receptor in facilitating acquisition and consolidation of associative memories.
triazole 1.1 retained the antinociceptive and antipruritic efficacies of a conventional KOR agonist, yet it did not induce sedation or reductions in dopamine release in mice, nor did it produce dysphoria as determined by intracranial self-stimulation
This study reports a cluster of compounds that are highly effective in enhancing remyelination and identifies kappa-opioid receptor (KOR) as a positive regulator for oligodendroglial differentiation, implicating KOR agonism as a potential strategy to accelerate remyelination.
GRK2 (显示 ADRBK1 ELISA试剂盒) upregulation causes kappa-opioid receptor desensitization in diabetic heart
Study showed that Dyn (显示 PDYN ELISA试剂盒)-A, the endogenous kappa opioid receptor agonist, significantly hyperpolarized and inhibited neurons in the paraventricular nucleus of mouse thalamus
Suggest that mixed cardiac ion channel blockade my mediated the antiarrhythmia actions of kappa-opioid receptor antagonist PD117,302.
Anti-nociception mediated by a KOR agonist is blocked by a DOR agonist
Findings suggest that activation of kappa opioid receptor (kappa-opioid receptor) reduces hyperglycemia in streptozotocin-induced diabetic mice.
findings show that, during prolonged heroin abstinence, delta opioid receptors regulate hedonic homeostasis, while mu opioid receptor (显示 OPRM1 ELISA试剂盒) signaling in serotonergic pathways and kappa opioid receptors together control social behaviors
a class of opioid receptors\; show selective affinity for the endogenous opioid dynorphin
, kappa-type opioid receptor
, opioid receptor, kappa 1
, kappa opioid receptor
, Opiate receptor, kappa-1
, opioid receptor, kappa 2