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中文名稱：小鼠去甲腎上腺素(NA)酶聯免疫試劑盒
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貨號：CSB-E07870m
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規格：96T/48T
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價格：￥3800/￥2500
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其他：
產品詳情
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產品描述：小鼠去甲腎上腺素(NA)酶聯免疫試劑盒（CSB-E07870m）為競爭法ELISA試劑盒，定量檢測血清、血漿樣本中的NA含量。小鼠去甲腎上腺素（NA）作為一種重要的神經遞質，在中樞神經系統和交感神經系統中參與調節生理過程，如感覺信號、注意力、清醒與睡眠、學習與記憶等。其釋放或信號傳遞的受損與精神疾病和神經退行性疾病相關。近年來，研究者開發了新型基因編碼的NA熒光探針，通過實時監測NA動態變化，為研究NA相關神經環路提供了重要工具。試劑盒檢測范圍為7.5 pg/mL-300 pg/mL，本試劑盒適用于神經生物學研究、應激反應機制探索、心血管藥理學實驗中對NA分泌水平的動態監測，也可用于評估抗高血壓藥物或神經調節劑對NA代謝通路的影響。本品僅用于科研，不用于臨床診斷，產品具體參數及操作步驟詳見產品說明書。
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別名：N/A
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縮寫：NA
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種屬：Mus musculus (Mouse)
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樣本類型：serum, plasma
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檢測范圍：7.5 pg/mL-300 pg/mL
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靈敏度：7.5 pg/mL
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反應時間：1-5h
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樣本體積：50-100ul
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檢測波長：450 nm
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研究領域：Neuroscience
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測定原理：quantitative
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測定方法：Competitive
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精密度：
Intra-assay Precision (Precision within an assay): CV%<15% Three samples of known concentration were tested twenty times on one plate to assess. Inter-assay Precision (Precision between assays): CV%<15% Three samples of known concentration were tested in twenty assays to assess. -
線性度：
To assess the linearity of the assay, samples were spiked with high concentrations of mouse noradrenaline in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. Sample Serum(n=4) 1:1 Average % 100 Range % 98-104 1:2 Average % 87 Range % 84-90 1:4 Average % 86 Range % 83-89 1:8 Average % 91 Range % 88-94 -
回收率：
The recovery of mouse noradrenaline 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 Type Average % Recovery Range Serum (n=5) 85 82-89 EDTA plasma (n=4) 97 94-100 -
標準曲線：
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. 
pg/ml OD1 OD2 Average 300 0.371 0.396 0.384 150 0.548 0.578 0.563 69 0.775 0.798 0.787 22.5 1.126 1.168 1.147 7.5 1.672 1.587 1.630 0 2.201 2.209 2.205 -
數據處理：
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貨期：3-5 working days
引用文獻
- Xiao‐Chai‐Hu‐Tang Ameliorates Depressive Symptoms via Modulating Neuro‐Endocrine Network in Chronic Unpredictable Mild Stress‐Induced Mice Y Feng, W Wang, Y Zhang, Y Feng,CNS Neuroscience & Therapeutics,2025
- Chronic stress disturbed the metabolism of homocysteine in mouse hippocampus and prefrontal cortex C Xue, B Liu, Y Zhao, X Wang, ZW Sun, F Xie, LJ Qian,Neuroscience,2024
- UVB Induces Sympathetic Nervous System Activation and Norepinephrine Secretion to Regulate The Skin Color of Mice Through the β2-AR/AP-1 Pathway in Epidermal Keratinocytes Q Deng, X Liu, X Wen, H Huang, H Tang,Inflammation,2025
- CAR T cells secreting NGF-neutralizing scFv enhance efficacy in clear cell renal cell carcinoma by relieving immunosuppression through immunosympathectomy P Yang, X Chen, F Yu, L Wang, M Li,Journal for Immunotherapy of Cancer,2024
- Exercise-induced anxiety impairs local and systemic inflammatory response and glucose metabolism in C57BL/6J mice I Gálvez, C Navarro, S Torres-Piles,Brain, Behavior, & Immunity-Health,2024
- Sleep Deprivation Triggers the Excessive Activation of Ovarian Primordial Follicles via β2 Adrenergic Receptor Signaling L Weng, H Hong, Q Zhang, C Xiao, Q Zhang,Advanced Science,/
- Immunoneuroendocrine, Stress, Metabolic, and Behavioural Responses in High-Fat Diet-Induced Obesity M del Carmen Navarro,Nutrients,2024
- Effect of quercetin on the progression of breast cancer in mice with chronic stress by regulating the polarization of microglia T Luo,Journal of Functional Foods,2024
- Peripheral administration of lipidized NPAF and NPFF analogs does not influence central food intake regulation but induces anxiety-like behavior V Strnadová,Neuropeptides,2024
- Kaempferol Improves Breast Cancer-Related Depression through the COX-2/PGE2 Pathway Q Zhu,IMR Press,2023
- Combined SGLT1 and 2 Inhibition Os Associated With Improved Glucose Control and Multi-Organ Protection in the Type 1 Diabetic Akimba Mouse L Herat,SSRN,2023
- Whitening of brown adipose tissue inhibits osteogenic differentiation via secretion of S100A8/A9 R Ramendra,iScience,2024
- SGLT1/2 inhibition improves glycemic control and multi-organ protection in type 1 diabetes. LY Herat,iScience,2023
- LncRNA Nron deficiency protects mice from diet-induced adiposity and hepatic steatosis B Liu,Metabolism,2023
- The Sympathetic Nervous System Regulates Sodium Glucose Co-Transporter 1 Expression in the Kidney J Matthews,Biomedicines,2023
- Hypothermia evoked by stimulation of medial preoptic nucleus protects the brain in a mouse model of ischaemia S Zhang,Nature communications,2022
- Local hyperthermia therapy induces browning of white fat and treats obesity Yu Li,Cell,2022
- Aminergic status in the brain of urokinase gene-deficient mice with malignant tumors growing in presence of chronic neurogenic pain YA Pogorelova,Journal of Clinical Oncology,2021
- Оказывает ли влияние изменение нейротрансмиттерного статуса мозга на рост перевивной меланомы? ОИ Кит,/,2021
- SGLT2 Inhibitor-Induced Sympathoexcitation in White Adipose Tissue: A Novel Mechanism for Beiging. JR Matthews,Biomedicines,2020
- Intestinal microbiota contributes to altered glucose metabolism in simulated microgravity mouse model Wang Y, et al,Faseb Journal,2019
- Intrauterine exposure to hyperglycemia retards the development of brown adipose tissue Yu DQ, et al,Faseb Journal,2019
- Acute tobacco smoke exposure exacerbates the inflammatory response to corneal wounds in mice via the sympathetic nervous system Xiao C, et al,Acta Crystallographica Section F-Structural Biology Communications,2019
- IL-25 induces beige fat to improve metabolic homeostasis via macrophage and innervation Lingyi Li, et al,BioRxiv,2018
- AMP-Activated Protein Kinase (AMPK) Regulates Energy Metabolism through Modulating Thermogenesis in Adipose Tissue Lingyan Wu.et al,ORIGINAL RESEARCH ARTICLE,2018
- p38α function in osteoblasts influences adipose tissue homeostasis. Rodr鉚guez-Carballo E.et al,FASEB J.,2015
- NMDA Receptor Antagonist Attenuates Bleomycin-Induced Acute Lung Injury. Yang Li, et al,PLoS One,2015
- Curcumin promotes browning of white adipose tissue in a norepinephrine-dependent way Wang S. et al,Biochem Biophys Res Commun,2015
- Intestinal gluconeogenesis is crucial to maintain a physiological fasting glycemia in the absence of hepatic glucose production in mice Penhoat A et al,Metabolism,2013
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