Standardized Measurements and Differential Spectroscopy in Microplates
Analytical Biochemistry, ISSN: 0003-2697, Vol: 296, Issue: 1, Page: 29-40
2001
- 10Citations
- 28Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations10
- Citation Indexes10
- 10
- CrossRef8
- Captures28
- Readers28
- 28
Article Description
Microplates (MPs) are excellent devices for the parallel processing of multiple samples for the spectroscopic analysis of chromophores and turbidity, for luminometric measurements, for cell culture applications, or simply for sample storage, library organization, and other high-throughput (HTP) processes. Disadvantages include an ill-defined pathlength, meniscus formation, evaporation, and cross-contamination. Here, we have developed a novel MP and lid system which can serve to minimize these drawbacks. Cup-like lids are inserted into MP wells. Thereby, liquid is pushed aside. The flat bottoms of the cup-like lids guarantee a planar interface and a defined pathlength. In addition, the devised MP system allows for differential spectroscopic analysis of multiple samples comparable to measurements in tandem cuvettes. This was shown by the investigation of the binding of reduced nicotinamide adenine dinucleotide to dihydrolipoamide dehydrogenase. The MP lid system described offers a low-cost solution for standardized spectrophotometric quantitations in any solvent compatible with the MP/lid material. In addition to the system's suitability for routine MP application, it should be advantageous as a simple and noninvasive method, i.e., no labeling and immobilization of analytes is required for detection of the interaction of molecules, for various HTP applications and drug screening purposes.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0003269701952315; http://dx.doi.org/10.1006/abio.2001.5231; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0035450953&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/11520029; https://linkinghub.elsevier.com/retrieve/pii/S0003269701952315; https://dx.doi.org/10.1006/abio.2001.5231
Elsevier BV
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