The compressed audio samples were converted to their respective spectrogram images and were analyzed.
The samples were converted to CO2 by combustion in sealed evacuated quartz tubes containing CuO.
The samples were converted to methyl ester derivatives by the protocol reported by Lepage and Roy (1986).
Zeolite samples were converted into the H-form by calcining them in the atmosphere of air at the temperature of 540 °C for 3 h.
The peak areas obtained from chromatographic analysis of all injected samples were converted to concentrations using the calibration responses of the neurochemical standards.
The concentration of various ions as obtained from chemical analysis of ground water samples were converted to milliequivalent/litre (meq/L) and used to derive certain parameters.
Equal aliquots of total RNA from samples were converted to cDNA with the High-Capacity cDNA Archive kit (Applied Biosystems), and qPCR reactions were performed in triplicate with 10 ng of cDNA and the TaqMan Universal PCR master mix (Applied Biosystems).
Using this standard curve, optical density from samples were converted to Arbitrary Units (AU).
Isolated RNA samples were converted to cDNA in 50 µl fractions using TaqMan® Reverse Transcription reagents (Applied Biosystems).
RNA samples were converted to cDNA using the High Capacity cDNA Archive Kit (Applied Biosystems, Foster City, CA).
Samples were converted to labeled, fragmented, cRNA per the Affymetrix protocol for use on the expression microarray.
