细胞技术/aCella™ AChE/100/CLACHE100

价格
¥43900.00
货号:CLACHE100
浏览量:127
品牌:Cell Technology
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商品描述
  • Description
  • Additional Information
  • Readable Documents
  • Assay Principle
  • Reviews

Key Benefits

  • Safe – Non Radioactive Enzyme activity assay.
  • Versatile: Nerve Gas, Pesticide Monitoring, drug screening Applications
  • Homogenous – One-step, no wash assay.
  • FAST – Results in 30 secs – 5 minutes.
  • Highly Sensitive
  • HTS – Adaptable for High Throughput format
  • Applications – Standard luminometer readout

Additional information

Kit Size

100, 500, 1000

We have developed a highly sensitive, very rapid, extremely simple assay for AChE activity, using the natural substrate, acetylcholine. As shown in Figure 1, a series of coupled enzyme reactions quickly translates the presence of active AChE into a change in the luminance of the reaction. First (reaction I), acetylcholine is hydrolyzed by the AChE to yield acetate and choline. The acetate and choline then enter a coupled enzyme reaction (reaction II) that results in consumption of ATP, and finally the ATP concentration is measured by the well-established luciferase method (reaction III). These reactions can occur simultaneously, and the result is generally obtained in five minutes or less. Inhibitors of AChE are readily detected by an increase in luminance due to reduced consumption of ATP.

The following reaction illustrates the sequence of events if AChE inhibitors are present:

Reaction I: AChE + Inhibitor  No Acetate and CholineReaction II: Coupled Enzyme Reaction + ATP arrow Reaction does not proceedReaction III: ATP (remaining) + Luciferase/Luciferin arrow LIGHT

acellatm_ache2-aFigure A. Tacrine (a mixed-mode inhibitor of AChE) was serially diluted in DI water. Next 10mL of the diluted Tacrine (x axis labeling represents mM final concentration of Tacrine) was added to a white opaque 96-well microplate along with 50 mL of component A (AChE enzyme). The samples were incubated for 5 minutes after which 50mL of component B was added to all the wells. Data were collected using a luminometer. Data shown represents T=2 minutes after the addition of component B.

acellatm_ache1-bFigure B. Malathion, a common pesticide, was first diluted in DMSO and subsequently serially diluted in Di water. 10μL of the diluted Malathion (x axis represents μM final concentration of Malathion) was added to a white opaque 96-well microplate followed by 50 μL of component A (AChE enzyme). The mixture was incubated for 15 minutes, after which 50 μL of component B was added to all the wells. Data were collected using a luminometer. Data shown is at T= 5 minutes. Data shown represents T=2.5 minutes after the addition of component B.

Document Title
aCella-AChEProtocol
aCella-AChE Datasheet
msds.aCella-AChE

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Cell Technology的Apo Active 3PE对活性人和鼠半胱天冬酶3具有高度特异性。其他测定需要利用基于肽的(DEVD)试剂,这些试剂倾向于与半胱天冬酶7和其他半胱天冬酶交叉反应。应用 –流式细胞仪,荧光显微镜或荧光酶标仪。产生定量和定性结果。发出强烈的积极信号。可以与其他抗体或染色剂一起使用。无需进行细胞裂解液或蛋白质印迹分析。单元可以固定,以后再分析。适用于人类,小鼠和大鼠细胞系。