WebThe BacTiter-Glo™ Microbial Cell Viability Assay is a homogeneous method to determine the number of viable bacterial cells in culture based on quantitation of ATP. The assay is designed for either single-tube or multiwell-plate formats for … WebJun 14, 2024 · The supernatant was discarded to remove ATP derived from dead bacteria and SBA reagents. The remaining bacterial pellets were resuspended in PBS, transferred to a white 96-well plate (Greiner Bio-One, Roma, Italy) and mixed 1:1 v: v with BacTiter-Glo Reagent (Promega, Southampton, UK). The reaction was incubated for 5 min at room …
BacTiter-Glo Microbial Cell Viability Assay from Promega
WebThe BacTiter-Glo Microbial Cell Viability Assay is a homogeneous method for determining the number of viable microbial cells in culture based on quantitation of the ATP present. A Luminescent Assay to Measure the Number of Viable Microbial Cells in Culture A homogeneous, single reagent assay Offers increased sensitivity, fast results WebMar 11, 2024 · The viability assay was performed using the BacTiter-GloTMMicrobial Cell Viability Assay (Promega Italia S.r.l., Milan, Italy), following the manufacturer’s instructions, at the time points of 24, 48, and 72 h. A Spark microplate reader (Tecan Trading AG, Switzerland) was used to detect luminescence. heart eye prescription glasses
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WebJun 5, 2012 · Promega 成功地开发出基于另一种萤火虫 Photinus pennsylvanica 的一种稳定形式的萤光素酶(Ultra-Glo TM 重组萤光素酶),使用一种能选 择在ATP 检测性能方面有所提高的性质。 另外,我们开发了一个专利配方,可以从不同 的微生物细胞中快速有效地提取ATP(表1)。 BacTiter-Glo TM 试剂中这两个基本因素的 结合使我们能够设计出在培养 … WebMar 20, 2024 · bactiter-glo assay Archives - Promega Connections bactiter-glo assay Wetlands, Water Quality and Rapid Assays Posted on March 20, 2024 by Michele Arduengo The storms of the previous day had moved eastward, leaving in their wake flooded farm fields and saturated roadside wetlands. At dusk, we loaded the Ford Escort wagon and … WebThe Viral ToxGlo™ Assay is a simple, quantifiable method of determining viral-induced cytopathic effects (CPE) in host cells caused by lytic virions. The assay measures cellular ATP as a surrogate measure of host cell viability. When CPE occurs due to viral infection, ATP depletion can be measured and correlated with viral burden. mount clifford residencies