武汉费斯德生物科技有限公司, NewEast Biosciences 中国办事处

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cAMP EIA Kit – No Acetylation X 5

Monoclonal cGMP EIA Kit - No Acetylation
5/5

¥1,595.00

货号:80204

规格: 5×96 well

库存状态:In Stock

           产品描述          

Product Highlight

  • Based on the unique mouse monoclonal anti-cAMP antibody
  • The only assay kit on the market with monoclonal anti-cAMP antibody (all other kits are based on polyclonal anti-cAMP antibodies)
  • The monoclonal anti-cAMP antibody displays much higher selectivity over cGMP and ATP than polyclonal anti-cAMP antibody
  • Avoids the batch-to-batch variations associated with polyclonal antibody productions from animals, thus providing the reproducibility

Product Description

Adenosine 3′, 5′-cyclic monophosphate (cyclic AMP; cAMP) modulates various physiological functions such as cardiovascular biology, learning and memory, olfaction, immune response, asthma and kidney function (1,2). cAMP is produced from ATP by adenylyl cyclases and is degraded by phosphodiesterases. Stimulation of adenylyl cyclases or inhibition of phosphodiesterases can increase cellular cAMP concentrations. Blockers of adenylyl cyclase-activating receptors and inhibitors of the cAMP-specific phosphodiesterases are used for treating human diseases. For example, blocking agents for cAMP-increasing beta-adrenergic receptors (beta-blockers) are used for treating abnormal heart rhythms, high blood pressure (hypertension), myocardial infarction and heart failure. Inhibitors of cAMP specific phosphodiesterase types 2 and 4 are being tested for cognition enhancement.
To screen for inhibitors or stimulators of cellular cAMP levels, it is essential to have a sensitive, selective and reproducible method to measure the cAMP concentrations. This is especially true for the initial screenings given the possible weaker effects of larger pools of compounds.
Currently available other ELISA kits measuring cAMP levels are based on the non-affinity-purified polyclonal anti-cAMP antibody. Despite the claimed selectivity, these polyclonal anti-cAMP antibodies display certain cross-reactivity with ATP. Given that ATP is the substrate for the cAMP production, it is very desirable to have an antibody with high specificity towards cAMP over ATP.
NewEast Biosciences cAMP ELISA kit is based on the unique mouse monoclonal anti-cAMP antibody. This monoclonal anti-cAMP antibody displays >108 fold of selectivity over ATP, cGMP, and other nucleoside analogues. NewEast Biosciences cAMP ELISA kit provides significantly improved sensitivity and selectivity over other kits based on polyclonal anti-cAMP antibodies. Our monoclonal anti-cAMP antibody-based ELISA kit also avoids the batch-to-batch variations associated with polyclonal antibody productions from animals, thus providing the reproducibility in the long run.

Principle Outline

NewEast Biosciences cAMP ELISA Kit is a competitive immunoassay to measure the cAMP levels, either from cell extracts or from in vitro adenylyl cyclase assays. Briefly, multi-well plates are coated with goat-anti-mouse serum. cAMP in cell extracts or in in vitro adenylyl cyclase assays will competitively bind to the monoclonal anti-cAMP antibody in the presence of fixed amounts of cAMP-conjugated horse-radish peroxidase or alkaline phosphatase. Known amounts of cAMP are used as standards to generate the calculation curve. After a short incubation, the excess reagents are washed away and substrate is added. The multi-well plates are then read on a microplate reader at 450 nm or 405 nm. The intensity of the yellow color is inversely proportional to the concentration of cAMP in samples. The measured optical density is used to calculate the concentration of cAMP in samples based on the curve from the cAMP standards.
           引用文献          
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33. Influence of cell confluence on the cAMP signalling pathway in vascular smooth muscle cells
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34. Influence of dopamine D1 receptor Ala229Thr polymorphism on receptor signal transduction
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37. Zebrafish phosvitin-derived peptide Pt5 inhibits melanogenesis via cAMP pathway
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38. A cardiac mitochondrial cAMP signaling pathway regulates calcium accumulation, permeability transition and cell death
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39. Characterization and expression of soluble guanylate cyclase in skins and melanocytes of sheep
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40. Dietary flavonoid luteolin attenuates uropathogenic Escherichia. Coli invasion of the urinary bladder
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41. Hypoxia-Inducible Factor-2α Limits Natural Killer T Cell Cytotoxicity in Renal Ischemia/Reperfusion Injury
J Am Soc Nephrol. 2016
42. MoRad6-mediated ubiquitination pathways are essential for development and pathogenicity in Magnaporthe oryzae
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43. Nuclear translocation of nuclear factor kappa B is regulated by G protein signaling pathway in arsenite-induced apoptosis in HBE cell line
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44. RNA polymerase III component Rpc9 regulates hematopoietic stem and progenitor cell maintenance in zebrafish
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45. The effects of IGF1 on the melanogenesis in alpaca melanocytes in vitro
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46. Comparative Effects of Urocortins and Stresscopin on Cardiac Myocyte Contractilit
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47. Effect of dobutamine on lung aquaporin 5 in endotoxine shock-induced acute lung injury rabbit
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48. Identification of a novel microRNA important for melanogenesis in alpaca (Vicugna pacos)
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49. Positive Effect of Carbon Sources on Natural Transformation in Escherichia coli: Role of Low-Level Cyclic AMP (cAMP)-cAMP Receptor Protein in the Derepression of rpoS
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50. Alteration of vascular reactivity in heart failure: Role of phosphodiesterases type 3 and 4
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51. cAMP–PKA inhibition of SK3 channel reduced both Ca2+ entry and cancer cell migration by regulation of SK3–Orai1 complex
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52. Comparative study of somatostatin-human serum albumin fusion proteins and natural somatostatin on receptor binding, internalization and activation
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55. Ischemia/Reperfusion-Induced CHOP Expression Promotes Apoptosis and Impairs Renal Function Recovery: The Role of Acidosis and GPR4
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56. Sex is a major determinant of neuronal dysfunction in Neurofibromatosis Type 1
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57. Three genes encoding citrate synthases in Saccharopolyspora erythraea are regulated by the global nutrient-sensing regulators GlnR, DasR, and CRP
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58. Opposing HDAC4 nuclear fluxes due to phosphorylation by β adrenergic activated PKA or by activity or Epac activated CaMKII in skeletal muscle fibres
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59. Subendocardial Increase in Reactive Oxygen Species Production Affects Regional Contractile Function in Ischemic Heart Failure
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60. Transgenic rescue of defective Cd36 enhances myocardial adenylyl cyclase signaling in spontaneously hypertensive rats
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61. Uncoupling of M1 muscarinic receptor/G-protein interaction by amyloid beta(1-42)
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62. Agonist-Dependent And -Independent Dopamine-1-Like Receptor Signalling Differently Regulates Downstream Effectors
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63. Antiarrhythmic effect of prolonged morphine exposure is accompanied by altered myocardial adenylyl cyclase signaling in rats
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