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Byosens GmbH LYTE96便攜式無標(biāo)記酶標(biāo)儀,便攜式酶聯(lián)**檢測儀

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  • 產(chǎn)品名稱:Byosens GmbH LYTE96便攜式無標(biāo)記酶標(biāo)儀,便攜式酶聯(lián)**檢測儀
  • 產(chǎn)品型號:LYTE96
  • 產(chǎn)品展商:Byosens GmbH
  • 產(chǎn)品文檔:無相關(guān)文檔
簡單介紹

BYOSENS LYTE96 THE FIRST PORTABLE LABEL-FREE MICROPLATE READER! yte96無標(biāo)記便攜生物傳感器是基于康寧Epic系統(tǒng)設(shè)計的,可進(jìn)行一系列細(xì)胞內(nèi)試驗的96孔微孔板讀出設(shè)備。lyte96將無線連接和集成電池結(jié)合放置到一個緊湊的結(jié)構(gòu)中,使得它方便移動和易于整合進(jìn)液體處理系統(tǒng)。主要是對系列廣泛的生物反應(yīng)進(jìn)行檢測,如信號轉(zhuǎn)導(dǎo)、細(xì)胞凋亡、細(xì)胞毒

產(chǎn)品描述

BYOSENS LYTE96**臺便攜式無標(biāo)記酶標(biāo)儀(便攜微孔板檢測器)

 

lyte96無標(biāo)記便攜生物傳感器系統(tǒng)介紹

 

lyte96無標(biāo)記便攜生物傳感器是基于康寧Epic系統(tǒng)設(shè)計的,可進(jìn)行一系列細(xì)胞內(nèi)試驗的96孔微孔板讀出設(shè)備。lyte96將無線連接和集成電池結(jié)合放置到一個緊湊的結(jié)構(gòu)中,使得它方便移動和易于整合進(jìn)液體處理系統(tǒng)。主要是對系列廣泛的生物反應(yīng)進(jìn)行檢測,如信號轉(zhuǎn)導(dǎo)、細(xì)胞凋亡、細(xì)胞**,貼壁、增殖和擴(kuò)散等。

lyte96無標(biāo)記便攜生物傳感器的工作原理是基于折射波導(dǎo)光柵光學(xué)生物傳感器。傳感器結(jié)構(gòu)由一個三層系統(tǒng):玻璃基板、薄膜光波導(dǎo)薄膜與光柵結(jié)構(gòu),和細(xì)胞/生物分子層。當(dāng)寬譜帶光照射時,生物傳感器反映光的特定波長是接近傳感器表面折射率的靈敏函數(shù)。通過 Epic系統(tǒng)測量細(xì)胞內(nèi)的粘合物事件或細(xì)胞內(nèi)蛋白質(zhì)運(yùn)動引起反射光的波長偏移。形成一系列波長偏移、波長、強(qiáng)度、時間之間的函數(shù)來進(jìn)行分析。

lyte96無標(biāo)記便攜生物傳感器的優(yōu)勢:

移動性: lyte96**設(shè)計之處是給使用者帶來了*大的靈活性。緊湊的結(jié)構(gòu)結(jié)合了無線連接和集成的電池使lyte96方便移動。這使得它對于研究人員和開發(fā)人員來說成為一個**的分析工具。

易用性: lyte96簡化了研發(fā)實驗室中的過程。實驗開始時不需要復(fù)雜的預(yù)置,直觀輔助的軟件保證了高水平的易用性。由于**技術(shù)體系,lyte96幾乎是免費維護(hù)。

數(shù)據(jù)分析:根據(jù)已建立的康寧Epic系統(tǒng),高敏性的lyte96可進(jìn)行寬光譜的細(xì)胞內(nèi)試驗,從開始試驗到幾天的時間都可以提供實時數(shù)據(jù)以便研究。 

 

1. 萊特96無標(biāo)記便攜生物傳感器

 

 

2.測量原理示意圖

 

1:在增殖試驗中,用lyte96實時監(jiān)測細(xì)胞數(shù)量,發(fā)現(xiàn)細(xì)胞數(shù)目和傳感器表面的質(zhì)量是成正比的。微孔板和lyte96放置在加濕的培養(yǎng)箱內(nèi)通過藍(lán)牙無線連接電腦。經(jīng)典增殖試驗中,A431細(xì)胞加入到孔中,記錄37?C的細(xì)胞生長。

 

2:動態(tài)質(zhì)量再分配(DMR)的測定

像許多其他的信號檢測,GPCR測定動態(tài)質(zhì)量再分配過程中(DMR)是由lyte96無標(biāo)記傳感器測定的。和A431細(xì)胞緩激肽試驗一樣,這個試驗是在室溫下進(jìn)行。得到的EC500.45 nm,這類似于從文獻(xiàn)的結(jié)果

參考文獻(xiàn):

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Camp, N. D. et al. Dynamic mass redistribution reveals diverging importance of PDZ-ligands for G protein-coupled receptor pharmacodynamics. Pharmacological. Research, 105, 13-21 (2016).

 

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Klepac, K. et al. The Gq signalling pathway inhibits brown and beige adipose tissue. Nat. Commun. 7, 10895 (2016).

 

2015

Hamamoto, A., Kobayashi, Y. & Saito, Y. Identification of amino acids that are selectively involved in Gi/o activation by rat melanin-concentrating hormone receptor 1. Cell. Signal. 27, 818–827 (2015).

 

Navarro, G. et al. Orexin – Corticotropin-Releasing Factor Receptor Heteromers in the Ventral Tegmental Area as Targets for Cocaine. J. Neurosci. 35, 6639–6653 (2015).

 

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2014

Beckert, U. et al. Biochemical and Biophysical Research Communications cNMP-AMs mimic and dissect bacterial nucleotidyl cyclase toxin effects. Biochem. Biophys. Res. Commun. 451, 497–502 (2014).

 

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Fang, Y. Label-Free Cell Phenotypic Drug Discovery. Comb. Chem. High Throughput Screen. 17, 566–578 (2014).

 

Fang, Y. Label-free drug discovery. Front. Pharmacol. 5, 1–8 (2014).

 

Febles, N. K., Ferrie, A. M. & Fang, Y. Label-Free Single Cell Kinetics of the Invasion of Spheroidal Colon Cancer Cells through 3D Matrigel. Anal. Chem. 86, 8842–8849 (2014).

 

Lee, M. Y. et al. A Comparison of Assay Performance Between the Calcium Mobilization and the Dynamic Mass Redistribution Technologies for the Human Urotensin Receptor. Assay Drug Dev. Technol. 12, 361–368 (2014).

 

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Ferrie, A. M., Zaytseva, N. & Fang, Y. Divergent Label-free Cell Phenotypic Overexpressed b2-Adrenergic Receptors. Sci. Rep. 4, 3828 (2014).

 

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 2013

Sundstr?m, L., Greasley, P. J., Engberg, S., Wallander, M. & Ryberg, E. Succinate receptor GPR91 , a G ai coupled receptor that increases intracellular calcium concentrations through PLC b. FEBS Lett. 587, 2399–2404 (2013).

 

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Morse, M., Sun, H., Tran, E., Levenson, R. & Fang, Y. Label-free integrative pharmacology on-target of opioid ligands at the opioid receptor family. BMC Pharmacol. Toxicol. 14, 1–18 (2013).

 

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Deng, H., Sun, H. & Fang, Y. Label-free cell phenotypic assessment of the biased agonism and efficacy of agonists at the endogenous muscarinic M3 receptors. J. Pharmacol. Toxicol. Methods 68, 1–24 (2014).

 

Zaytseva, N. et al. Resonant waveguide grating biosensor-enabled label-free and fluorescence detection of cell adhesion. Sens. Actuators B Chem. 1–17 (2013).

 

Zhao, H., French, J. B., Fang, Y. & Benkovic, S. J. The purinosome, a multi-protein complex involved in the de novo biosynthesis of purines in humans. Chem. Commun. (Camb). 49, 1–17 (2014).

 

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