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The air samplers were analyzed at the Exposure Assessment Facility at the Johns Hopkins Bloomberg School of Public Health (JHSPH) for nicotine content analysis by gas chromatography technique.
These samplers were analyzed for PM10 and lead by Quanzhou Environmental Monitoring (Quanzhou, China), a professional institution for environmental monitoring, by weighing and by graphite furnace atomic absorption spectrophotometry, respectively.
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The material collected by the passive samplers was analyzed using a highly sensitive protocol involving thermal desorption followed by GC MS.
The amount of influenza viral RNA contained in the samplers was analyzed using quantitative real-time reverse-transcription PCR (qPCR) targeting the matrix gene M1.
Runoff, triggered by storm water events, was collected using ISCO auto-samplers from June 2010 to August 2011 and the samples were analyzed for TSS, turbidity, biochemical oxygen demand, electrical conductivity, and pH.
Ten dummy datasets with different randomizations of every sequence were analyzed by MOTIF SAMPLER using background model orders 0 3.
The concentrations were analyzed by accredited laboratories specializing in analyzing the samplers, and were reported as average values across the 7-day measurement period.
Her wardrobe was analyzed and re-analyzed.
The main components profile of SHT was analyzed at the 254 nm UV wavelength using the Elite Lachrom HPLC system (Hitachi High-Technologies Co., Tokyo, Japan) consisting of pump L-21300), auto-sampler (L-2200), column oven L-23500), andiodede array UV/VIS detector L-24555).
Twenty-one days of integrative accumulation was conducted in laboratory scale experiments, and the accumulated PFASs in the samplers were eluted and analyzed by high performance liquid chromatography coupled with tandem mass spectrometry (HPLC MS/MS).
The samplers were desorbed with carbon disulfide, shaken for 30 minutes and analyzed by gas chromatography coupled with mass spectrometry.
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