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Calibration curves were obtained by analyzing standards prepared from authentic standards (Steraloids) and extracted with the method used for samples.
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The accuracy of the proposed methods was evaluated by analyzing standard solutions of ebastine.
The accuracy of the proposed method was evaluated by analyzing standard solutions of EBS.
The analytical procedure was validated by comparing predicted and experimental values of sediment samples and by analyzing standard reference material.
The proprietary technology works much like a video scaler, analyzing standard definition (compressed) audio signals like MP3 audio files and upscales them to 192 KHz resulting in higher quality audio.
Absolute copy numbers of GrB and GAPDH mRNA were determined by simultaneously analyzing standard titrations of GrB and GAPDH plasmids.
The LOD and LOQ were calculated by repeatedly analyzing standard replicates over a period of 3 months.
The calibration curve was checked by analyzing standard solutions of each analyte at eight different levels.
Accuracy for blood lead and mercury was verified by analyzing standard reference material from the National Institute of Standards and Technology (Gaithersburg, MD, USA).
We determined the accuracy of methods by means of analyzing standard reference material 1640 [National Institute of Standards and Technology NISTT) Gaithersburg, MD, USA].
Agreement of HPLC data with analyzed standards prior to sample analyses and in between ten sample runs were satisfactory.
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