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CS0010

Sigma-Aldrich

β-分泌酶(BACE1) 活性检测试剂盒(荧光法)

1 kit sufficient for 250 reactions

同義詞:

BACE1 活性检测试剂盒(荧光法)

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About This Item

分類程式碼代碼:
12161503
NACRES:
NA.84

品質等級

用途

 kit sufficient for 250 reactions

運輸包裝

wet ice

儲存溫度

−20°C

基因資訊

human ... BACE1(23621)

生化/生理作用

作为一种跨膜蛋白酶,BACE1负责切割淀粉样前体蛋白 (APP) 的β位点来产生β淀粉样肽 (Aβ)。大脑中Aβ积累是阿尔茨海默氏症的主要病因。BACE1是抑制剂药物研发的靶点。

適合性

该试剂盒包含有效检测BACE1活性所需的全部试剂。其中包含筛选潜在BACE1抑制剂的酶。该检测基于荧光共振能量转移 (FRET) 技术,即在BACE1切割底物后观测增强的荧光信号。

僅套裝組件

產品號碼
描述

  • Fluorescent Assay Buffer 50 mL

  • Stop Solution 15 mL

  • Substrate (MOCA-SEV-NL-DAEFR-DNP-RR) 500 μL

  • Assay Standard 140 μL

  • BACE1 (β−Secretase) 300 units 100 μL

儲存類別代碼

10 - Combustible liquids


分析證明 (COA)

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Vijay K Nuthakki et al.
Bioorganic chemistry, 90, 103062-103062 (2019-06-21)
Alkaloids have always been a great source of cholinesterase inhibitors. Numerous studies have shown that inhibiting acetylcholinesterase as well as butyrylcholinetserase is advantageous, and have better chances of success in preclinical/ clinical settings. With the objective to discover dual cholinesterase
Lucas J Gutierrez et al.
Journal of biomolecular structure & dynamics, 35(2), 413-426 (2016-01-28)
We report here two new small-size peptides acting as modulators of the β-site APP cleaving enzyme 1 (BACE1) exosite. Ac-YPYFDPL-NH2 and Ac-YPYDIPL-NH2 displayed a moderate but significant inhibitory effect on BACE1. These peptides were obtained from a molecular modeling study.
L Hong et al.
Biochemical Society transactions, 30(4), 530-534 (2002-08-28)
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Terrusnolides A-D (1-4), four butenolides were isolated from an endophytic Aspergillus from Tripterygium wilfordii. The structures of 1-4 were established by comprehensive spectroscopic analyses and electronic circular dichroism (ECD) calculation. It is interesting that 1 was a butenolide derived by
Raúl Horacio Camarillo-López et al.
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Alzheimer's disease (AD) is a neurodegenerative disease with no cure nowadays; there is no treatment either to prevent or to stop its progression. In vitro studies suggested that tert-butyl-(4-hydroxy-3-((3-(2-methylpiperidin-yl)propyl)carbamoyl)phenyl) carbamate named the M4 compound can act as both β-secretase and

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