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The azo adduct formed was processed as described above.
The Ni-doped BZT sample was processed as described in [10, 11, 12, 13, 14].
The reaction mixture was vortex mixed for 10 s and incubated at 50°C for 15 min. The azo adduct formed was processed as described above, and the absorbance reading was taken at 470 nm using acetonitrile as blank solvent.
The mixture was vortex mixed for 10 s and incubated at 50°C for 15 min. For each sample, the azo adduct formed was processed as described above; the absorbance reading was recorded at 470 nm.
For the estimation of total protein by the method of Lowry et al. (1951), 0.5 g of a frozen muscle was processed as described before but homogenized in 4 ml ice-cold 0.5 N NaOH.
For genomic DNA isolation, blood was processed as described above.
Compilation of images from LSCM was processed as described below.
Data was processed as described by Wu et al. [70].
Total RNA was processed as described earlier [50].
Cord blood was processed as described previously by sequential Ficoll density gradient purification [56].
Every microarray in the experiment was processed as described above, including the Mock arrays.
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