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Concentrations of dissolved 1-MCP were monitored by analysis of headspace atmosphere over aqueous 1-MCP solutions in sealed jars.
The kinetics of the US-assisted enzymatic hydrolysis was monitored by analysis of the target compounds using liquid chromatography tandem mass spectrometry.
Each stage was monitored by analysis in 12% SDS polyacrylamide gels.
Polymerization was monitored by analysis of products on 20% sequencing gels [59].
Blood stage infections were monitored by analysis of Giemsa-stained blood smears of tail blood collected on day 4 10 after inoculation of sporozoites or infection by mosquito bite.
Toxin B-induced intoxication was monitored by analysis of the glucosylation status of Rac1 in HT-29 cell lysates, using a specific anti-Rac1 antibody that recognizes only non-glucosylated Rac1.
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Differentiation of CD34+ cells was monitored by morphological analysis of MGG-stained cytospins and by flow-cytometric analysis of CD34, CD38 and CD14 surface antigen expression.
Photodegradation reaction experiments were monitored by HPLC analysis.
The UV curing process was monitored by FTIR analysis.
The functional groups in the PVC-matrix nanocomposite films were also monitored by FTIR analysis.
Concentrations of glycerol and 1,3PD in the media were monitored by HPLC analysis.
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