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Rat Atrial Natriuretic Peptide,ANP ELISA Kit

  • 中文名称:
    大鼠心钠肽(ANP)酶联免疫试剂盒
  • 货号:
    CSB-E12982r
  • 规格:
    96T/48T
  • 价格:
    ¥3600/¥2500
  • 其他:

产品详情

  • 产品描述:

    This Rat NPPA ELISA Kit was designed for the quantitative measurement of Rat NPPA protein in serum, plasma, cell culture supernates, tissue homogenates, cell lysates. It is a Sandwich ELISA kit, its detection range is 7.8 pg/mL-500 pg/mL and the sensitivity is 1.95 pg/mL .

  • 别名:
    NppaNatriuretic peptides A ELISA Kit; Prepronatriodilatin) [Cleaved into: Atrial natriuretic factor ELISA Kit; ANF ELISA Kit; Atrial natriuretic peptide ELISA Kit; ANP); Auriculin-B; Auriculin-A; Atriopeptin-1 ELISA Kit; Atriopeptin I); Atriopeptin-2 ELISA Kit; Atriopeptin II); Atriopeptin-3 ELISA Kit; Atriopeptin III)] ELISA Kit
  • 缩写:
  • Uniprot No.:
  • 种属:
    Rattus norvegicus (Rat)
  • 样本类型:
    serum, plasma, cell culture supernates, tissue homogenates, cell lysates
  • 检测范围:
    7.8 pg/mL-500 pg/mL
  • 灵敏度:
    1.95 pg/mL
  • 反应时间:
    1-5h
  • 样本体积:
    50-100ul
  • 检测波长:
    450 nm
  • 研究领域:
    Cardiovascular
  • 测定原理:
    quantitative
  • 测定方法:
    Sandwich
  • 精密度:
    Intra-assay Precision (Precision within an assay): CV%<8%
    Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10%
    Three samples of known concentration were tested in twenty assays to assess.
  • 线性度:
    To assess the linearity of the assay, samples were spiked with high concentrations of rat ANP in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
     SampleSerum(n=4)
    1:5Average %97
    Range %92-105
    1:10Average %94
    Range %89-97
    1:20Average %91
    Range %87-95
    1:40Average %92
    Range %86-96
  • 回收率:
    The recovery of rat ANP spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
    Sample TypeAverage % RecoveryRange
    Serum (n=5) 8782-95
    EDTA plasma (n=4)9690-102
  • 标准曲线:
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
    pg/mlOD1OD2AverageCorrected
    5002.494 2.595 2.545 2.423
    2501.722 1.823 1.773 1.651
    1251.110 1.131 1.121 0.999
    62.50.615 0.646 0.631 0.509
    31.20.407 0.396 0.402 0.280
    15.60.307 0.296 0.302 0.180
    7.80.199 0.196 0.198 0.076
    00.123 0.121 0.122  
  • 数据处理:
  • 货期:
    3-5 working days

引用文献

产品评价

靶点详情

  • 功能:
    Hormone that plays a key role in mediating cardio-renal homeostasis, and is involved in vascular remodeling and regulating energy metabolism. Acts by specifically binding and stimulating NPR1 to produce cGMP, which in turn activates effector proteins, such as PRKG1, that drive various biological responses. Regulates vasodilation, natriuresis, diuresis and aldosterone synthesis and is therefore essential for regulating blood pressure, controlling the extracellular fluid volume and maintaining the fluid-electrolyte balance. Also involved in inhibiting cardiac remodeling and cardiac hypertrophy by inducing cardiomyocyte apoptosis and attenuating the growth of cardiomyocytes and fibroblasts. Plays a role in female pregnancy by promoting trophoblast invasion and spiral artery remodeling in uterus, and thus prevents pregnancy-induced hypertension. In adipose tissue, acts in various cGMP- and PKG-dependent pathways to regulate lipid metabolism and energy homeostasis. This includes upregulating lipid metabolism and mitochondrial oxygen utilization by activating the AMP-activated protein kinase (AMPK), and increasing energy expenditure by acting via MAPK11 to promote the UCP1-dependent thermogenesis of brown adipose tissue. Binds the clearance receptor NPR3 which removes the hormone from circulation.; May have a role in cardio-renal homeostasis through regulation of natriuresis, diuresis, vasodilation, and inhibiting aldosterone synthesis. In vitro, promotes the production of cGMP and induces vasodilation. May promote natriuresis, at least in part, by enhancing prostaglandin E2 synthesis resulting in the inhibition of renal Na+-K+-ATPase. However reports on the involvement of this peptide in mammal blood volume and blood pressure homeostasis are conflicting; according to a report, in vivo it is not sufficient to activate cGMP and does not inhibit collecting duct transport nor effect diuresis and natriuresis. Appears to bind to specific receptors that are distinct from the receptors bound by atrial natriuretic peptide and vessel dilator. Possibly enhances protein excretion in urine by decreasing proximal tubular protein reabsorption.; May have a role in cardio-renal homeostasis through regulation of natriuresis, diuresis, and vasodilation. In vitro, promotes the production of cGMP and induces vasodilation. May promote natriuresis, at least in part, by enhancing prostaglandin E2 synthesis resulting in the inhibition of renal Na+-K+-ATPase. However reports on the involvement of this peptide in mammal blood volume and blood pressure homeostasis are conflicting; according to a report, in vivo it is not sufficient to activate cGMP and does not inhibit collecting duct transport nor effect diuresis and natriuresis. Appears to bind to specific receptors that are distinct from the receptors bound by the atrial natriuretic and long-acting natriuretic peptides. Possibly functions in protein excretion in urine by maintaining the integrity of the proximal tubules and enhancing protein excretion by decreasing proximal tubular protein reabsorption.; May have a role in cardio-renal homeostasis through regulation of diuresis and inhibiting aldosterone synthesis. In vitro, promotes the production of cGMP and induces vasodilation. May promote natriuresis, at least in part, by enhancing prostaglandin E2 synthesis resulting in the inhibition of renal Na+-K+-ATPase. May have a role in potassium excretion but not sodium excretion (natriuresis). Possibly enhances protein excretion in urine by decreasing proximal tubular protein reabsorption.; Hormone produced in the kidneys that appears to be important for maintaining cardio-renal homeostasis. Mediates vasodilation, natriuresis and diuresis primarily in the renal system, in order to maintain the extracellular fluid volume and control the fluid-electrolyte balance. Specifically binds and stimulates cGMP production by renal transmembrane receptors, likely NPR1. Urodilatin not ANP, may be the natriuretic peptide responsible for the regulation of sodium and water homeostasis in the kidney.; May have a role in cardio-renal homeostasis through regulation of natriuresis and vasodilation. In vivo promotes natriuresis and in vitro, vasodilates renal artery strips.; May have a role in cardio-renal homeostasis through regulation of natriuresis and vasodilation. In vivo promotes natriuresis and in vitro, vasodilates renal artery strips.; May have a role in cardio-renal homeostasis through regulation of regulation of natriuresis and vasodilation. In vivo promotes natriuresis. In vitro, vasodilates intestinal smooth muscle but not smooth muscle strips.; May have a role in cardio-renal homeostasis through regulation of natriuresis and vasodilation. In vivo promotes natriuresis. In vitro, selectively vasodilates intestinal and vascular smooth muscle strips.; May have a role in cardio-renal homeostasis through regulation of natriuresis and vasodilation. In vivo promotes natriuresis. In vitro, selectively vasodilates intestinal smooth muscle but not vascular smooth muscle strips.
  • 基因功能参考文献:
    1. we suggest that the order of secretagogue effect of ET family on ANP secretion was ET-1>/=ET-2>>ET-3>s6C and ET-1-induced atrial natriuretic peptide secretion negatively regulates the pressor effect of ET-1. PMID: 27208702
    2. Despite preserved LV structure and function, treatment with GYY increased the levels of the natriuretic peptides ANP and BNP in association with enhanced cyclic GMP levels, paralleled by higher cGMP-dependent protein kinase type I (cGKI) protein levels PMID: 26254181
    3. Angiotensin IV stimulates ANP secretion and concentration via the IRAP and PI3K-Akt-mTOR signaling pathway. PMID: 25451332
    4. augmentation of inhibitory effect on basal motility by ANP in experimental colitis may be due an increased expression of colonic natriuretic peptide receptor-A mRNA PMID: 26660905
    5. ANP mRNA and protein are decreased in diabetic cardiomyopathy. PMID: 26446774
    6. This is due to the fact that ANP is the main hormone of the natriuretic peptide system involved in the regulation of blood pressure in normal conditions, while BNP is the principal regulator of pressure in cardiovascular pathology PMID: 27228659
    7. These results suggest that chronic treatment with nimesulide or NS-398 attenuated hypertension and cardiac hypertrophy partly through ANP release in 2K1C rats. PMID: 25846103
    8. expression arrhythmic in heart and not influenced by rotating light-dark regimens PMID: 25669688
    9. These findings demonstrate an important contributory role of ANP in the OT induced protection in myocardial ischaemia reperfusion. OT also reduced lipid peroxidation with a NO-dependent mechanism. PMID: 25126708
    10. BMP antagonist Noggin was able to inhibit stretch and hypertrophic agonist induced BNP and ANP expression. PMID: 25218476
    11. These findings suggest that HIF-1alpha and ANP, synthesized by the kidney, are involved in an adaptive mechanism in response to a sodium overload. PMID: 24689065
    12. Resistance training did not induce any change in vasopressin levels, and atrial natriuretic peptide levels did not change significantly. PMID: 23551170
    13. NPPA acts on the NPR1 receptor, is expressed in rat dorsal root and trigeminal ganglia, and the spinal cord. PMID: 25123163
    14. Provide direct evidence for the presence and synthesis of ANP and its receptors in both neuronal and non-neuronal cells within the cochlear spiral ganglion. PMID: 24333928
    15. the present study delivers a cooperative mechanism where Anxa6 potentiates ANP-dependent counterhypertrophic responses in cardiomyocytes by facilitating regulated traffic of pro-ANP. PMID: 24403064
    16. We conclude that D1R may play a major role in the ANP resistance observed in puromycin aminonucleoside-induced nephrotic syndrome . PMID: 23956981
    17. a direct evidence for the presence and synthesis of ANP as well as its receptors in the cochlear Spiral ganglion neurons, suggesting a possible role for ANP in modulating the neuronal functions of Spiral ganglion neurons via its receptors PMID: 23578746
    18. Endogenously released ACh tonically stimulates ANP secretion from atrial cardiomyocytes via activation of M2 mAChR-Gi/o-KACh(+) channel signaling. PMID: 23913708
    19. These results outline a PARP-1-dependent signal transduction mechanism that links contraction rate and Ca(2+) mobilization with the expression of genes underlying morphological changes in cardiomyocytes. PMID: 21635224
    20. ANP might be synthesized and secreted by marginal cells of stria vascularis, and it could play an important role in modulating the microenvironment of the inner ear. In addition, ANP might contribute to development and growth process of cochlea. PMID: 21552198
    21. ANF signals via natriuretic peptide receptor-C coupled to the phospholipase C-protein kinase C pathway to increase secretin-induced efflux of cAMP, probably through MPR-4 in pancreas PMID: 21237168
    22. Comparison of vasopressin (VP) to atrial natriuretic peptide (ANP) suggests that in early resistance training, VP release to bloodstream is higher than ANP release; the antidiuretic action of VP should prevail over ANP. PMID: 21287975
    23. Syntaxin-4 and VAMP-1 and VAMP-2 regulate cardiac myocyte exocytosis of ANP. PMID: 20801128
    24. The right ventricle is not a major source of cardiac ANP release in normoxia- or hypoxia-adapted rats. PMID: 20691705
    25. Results describe the involvement of myogenin and GATA4, two tissue-specific transcription factors, and the atrial natriuretic factor promoter, in cardiac transcriptional activity. PMID: 20384792
    26. found a close correlation between pulmonary embolism degree and gene-expression of ANP, and BNP in the cardiac chambers with a selective increase in the right chambers of the heart PMID: 20559433
    27. Results suggest that urotensin-II stimulates high stimulation frequency-induced ANP secretion partly through the urotensin receptor and the PLC/PI3K/PKC pathway. PMID: 19896516
    28. Leptin inhibits ANP secretion through nitric oxide without changing basal or isoproterenol-induced ANP secretion in rats. PMID: 20071611
    29. Mechanical overload in combined models of hypertension determines the evolution of hypertrophy and synthesis and secretion of ANP and BNP. PMID: 20139323
    30. The distribution of ANP after local irradiation of the rat heart depends on the severity of the pathological/structural changes (i.e. myocyte degeneration and fibrosis). PMID: 12020441
    31. ANP reduced TNFalpha release possibly by influencing post-translational processing of TNFalpha in LPS-activated KCs. In addition, we demonstrated that ANP enhances phagocytosis in KCs. PMID: 12022755
    32. ANP expression increased in rat atria throughout the prenatal and postnatal periods, except for a decrease in ANP expression in ventricles from prenatal day 21 onwards; it may have antimitogenic/antiproliferative effects in trabecular myocytes PMID: 12389741
    33. role in hypoxic activation of atrial natriuretic peptide gene promoter PMID: 12413399
    34. antral ANP and somatostatin secretion are linked by paracrine feedback pathways: endogenous ANP, acting via the NPR-A receptor, stimulates somatostatin secretion, and endogenous somatostatin, acting via the sst2 receptor, inhibits ANP secretion PMID: 12527142
    35. Mechanisms of hepatocyte protection against hypoxic injury by atrial natriuretic peptide. ANP recruits 2 independent signal pathways, which further transduce ANP signals to p38 MAPK, that are responsible for ANP protection against hypoxic injury. PMID: 12540777
    36. findings support that ANF exerts a stimulatory effect on pancreatic exocrine secretion mediated by NPR-C receptors coupled to the phosphoinositide pathway PMID: 12829435
    37. Cardiac expression of ANF demonstrated a time-related increase in ANF mRNA. PMID: 14575315
    38. The present study is the first to show linkage between Nppa marker and blood pressure in the rat. p. 935 PMID: 14678232
    39. Atrial natriuretic peptide expressed in the supraoptic nucleus acts as a peptidergic neurotransmitter involved in water and salt regulation during pregnancy and postpartum. PMID: 15117337
    40. Recruitment of PAM-1 to secretory vesicles depends on intact N-terminal proANP and on the lumenal domain of PAM-1. Conversely, PAM-1 participates in shaping the proANP-secretory vesicles. PMID: 15539631
    41. ANP induces MKP-1. ANP is a novel endogenous activator of endothelial Rac1 and Nox/Nox2. PMID: 15569826
    42. The downregulation of ANP and NPRC in retinas of diabetic rats suggests a role for this peptide in experimental diabetic retinopathy. PMID: 15789000
    43. ANP interferes with lysophosphatydic acid-induced DNA synthesis and ROS production. PMID: 16010968
    44. SERCA2alpha gene down-regulation in the non-infarcted myocardium of rats with MI does not correlate with ANP gene upregulation, suggesting that the two genes are not antithetically regulated. PMID: 16087130
    45. Atrial natriuretic peptides are located in mast cell secretory granules and released by mechanism of degranulation. PMID: 16246270
    46. The ANP might play a role on the synthesis of the oxytocin since ANP and its mRNA appear earlier than oxytocin. PMID: 16377580
    47. atrial natriuretic peptide, urodilatin, guanylin and uroguanylin interact in rat kidney PMID: 16814407
    48. The ET-1-induced increase in cell area, ANF mRNA expression and (3)H-phenylalanine incorporation in ET-1-treated NRVM were decreased by NHE-1 or NCX(rev) inhibition. PMID: 16859700
    49. The results indicate that distinct differences in ANF transcriptional regulation exist in vivo in the adult heart as compared with neonatal cardiomyocytes. PMID: 16909307
    50. Blocking nuclear translocation and subsequent binding of pSmad2 and pSmad3 to TGF-beta-Smad response elements in ECM genes may be responsible for the inhibitory effects of ANP on TGF-beta-induced expression of ECM molecules. PMID: 17038494

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  • 亚细胞定位:
    [Long-acting natriuretic peptide]: Secreted.; [Vessel dilator]: Secreted.; [Kaliuretic peptide]: Secreted.; [Urodilatin]: Secreted.; [Atrial natriuretic peptide]: Secreted. Perikaryon. Cell projection.; [Atriopeptin-3]: Secreted.
  • 蛋白家族:
    Natriuretic peptide family
  • 组织特异性:
    High levels of expression in the atria compared to the ventricles. Very low levels of expression detected in extracardiac tissues such as the brain, hypothalamus, pituitary, lung and aorta.; [Auriculin-A]: Atria (at protein level).; [Auriculin-B]: Atria (
  • 数据库链接:

    KEGG: rno:24602

    STRING: 10116.ENSRNOP00000011005

    UniGene: Rn.2004