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The algorithm reduces the variability of assays performed across different reagent and array batches, methods of sample preservation, multiple personnel, and among different laboratories.
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The chemicals industry, for example, keeps its production lines running in continuous processes that are more automated and efficient than the batch methods used by drug makers.
These batch methods have essentially two drawbacks.
Batch methods, while simple, cannot be used for all enzymes.
Batch methods are better than continuous processes and they facilitate testing of more variables as well.
Batch methods showed 56 63% of adsorption with A. niger, and 44 59% with A. terreus.
The detection limit in potentiometric measurements is lower than in batch methods.
Batch methods not relying on discretized state-spaces include the ML-PDA [9] and Histogram PMHT [10] algorithms.
Simple batch methods were proposed to determine Y, kd, μmax, and Ks, which are important for NDBPR process design.
The in situ ATR- FTIR method used is also advantageous compared to batch methods since it admits molecular level information of adsorbed species in real time.
The fluoride adsorption as a function of pH, initial fluoride concentration, EGANaCl dose, temperature, co-ions and cycles of regeneration was studied using batch methods.
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