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用于蛋白激酶A的转录筛选激酶检测方法的开发以及数据与滤膜结合检测形式的一致性证明。

Development of a Transcreener kinase assay for protein kinase A and demonstration of concordance of data with a filter-binding assay format.

作者信息

Huss Karen L, Blonigen Pauline E, Campbell Robert M

机构信息

Lilly Research Laboratories A Division of Eli Lilly and Company, Indianapolis, Indiana 46285, USA.

出版信息

J Biomol Screen. 2007 Jun;12(4):578-84. doi: 10.1177/1087057107300221. Epub 2007 Apr 4.

Abstract

A Transcreener kinase fluorescence polarization (FP) assay has been developed for the serine/threonine kinase protein kinase A (PKA). The PKA Transcreener kinase assay is an homogenous, competitive antibody-based FP assay that uses Far Red Alexa Fluor 633-labeled adenosine 5' disphosphate (ADP) tracer and mouse monoclonal anti-ADP antibody. The Transcreener PKA assay was validated with both known PKA inhibitors and library compounds. The Transcreener PKA assay is resistant to low-wavelength (or common) fluorescent interference from small-molecule library compounds and generates IC50 results comparable with current radioactive filter-binding assay.

摘要

已开发出一种用于丝氨酸/苏氨酸激酶蛋白激酶A(PKA)的转录筛选激酶荧光偏振(FP)测定法。PKA转录筛选激酶测定法是一种基于抗体的均相竞争性FP测定法,它使用远红Alexa Fluor 633标记的腺苷5'二磷酸(ADP)示踪剂和小鼠单克隆抗ADP抗体。转录筛选PKA测定法已通过已知的PKA抑制剂和文库化合物进行了验证。转录筛选PKA测定法对小分子文库化合物的低波长(或常见)荧光干扰具有抗性,并产生与当前放射性滤膜结合测定法相当的IC50结果。

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