首页> 外文期刊>American Journal of Tropical Medicine and Hygiene >Development of an Alamar BlueTM Viability Assay in 384-Well Format for High Throughput Whole Cell Screening of Trypanosoma brucei brucei Bloodstream Form Strain 427
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Development of an Alamar BlueTM Viability Assay in 384-Well Format for High Throughput Whole Cell Screening of Trypanosoma brucei brucei Bloodstream Form Strain 427

机译:用于高通量布鲁氏锥虫布鲁氏菌血流形式菌株全细胞筛选的384孔格式Alamar BlueTM活力测定方法的开发

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摘要

There is an urgent need for new compounds for the drug development pipeline for treatment of patients with African sleeping sickness. One approach for identifying such compounds is by high throughput screening (HTS) of compound collections. For time and cost considerations, there is a need for the development of an assay that uses at least 384-well formats. To our knowledge, there are currently no viability assays for whole cell screening of trypanosomes in the 384-well plate format. We have developed and optimized an Alamar Blue viability assay in a 384-well format for Trypanosoma brucei brucei bloodstream form strain 427 (BS427). The assay had a Z' > 0.5 and tolerated a final dimethyl-sulfoxide concentration of 0.42%. Drug sensitivity was compared with those reported from previously developed 96-well methods and was found to be comparable. The sensitivity and cost benefit of the Alamar Blue assay make it an excellent candidate for HTS application.
机译:迫切需要用于药物开发的新化合物 管道,以治疗非洲昏睡病患者。 一种识别此类化合物的方法是通过高通量 < / sup>筛选(HTS)化合物集合。出于时间和成本方面的考虑,需要开发至少使用384孔形式的分析方法。据我们所知,目前尚无用于384孔板形式锥虫小体全细胞筛查的生存力测定法。我们已经开发并优化了384孔格式的锥虫布鲁氏菌血流427菌株(BS427)的Alamar Blue生存力测定法。测定 的Z'> 0.5,并且最终的二甲基亚砜浓度 为0.42%。将药物敏感性与先前开发的96孔方法报道的 进行比较,发现 是可比的。 Alamar Blue 分析的灵敏性和成本优势使其成为HTS应用的理想选择。

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    Eskitis Institute for Cell and Molecular Therapies, GriffithUniversity, Nathan, Queensland, Australia;

    Eskitis Institute for Cell and Molecular Therapies, GriffithUniversity, Nathan, Queensland, Australia;

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