Er 3+-related absorption bands were recorded using a white light pump source together with an optical spectrum analyzer.
Amplification products were separated electrophoretically in 1% agarose gel, and ethidium bromide-stained bands were recorded using a Gel-Doc 2000 system (Bio-Rad).
Bands were recorded using a BCIP/NBT color development kit (Promega, Madison, WI, USA).
Bands were recorded using BCIP/NBT color development kit (Promega, Madison, WI, USA).
Bands were recorded using BCIP/NBT color development kit (Promega, Madison,W1, USA).
The activity was detected by WB analysis and the bands were recorded using the BCIP/NBT color development kit (Promega).
After silver staining, electrophoresis bands were recorded using the Banscan software, for the same migration distance, positive band was recorded as "1," negative band as "0," and failure of amplification as "9".
The EEG was recorded using Cognitrace software (ANT Software, Enschede, The Netherlands), and was amplified using an ANT amplifier, with a half-amplitude band pass of 0.016 100 Hz.
These antibodies were detected with a 1 10,000 dilution of the corresponding horseradish peroxidase-conjugated secondary antibody from Jackson ImmunoResearch Laboratories (West Grove, PA), and Enhanced Chemiluminescence reagents (EMD Millipore, Billerica, MA) and band intensities were recorded using a CCD camera-based imager (MicroChemi 4.2; FroggaBio, Toronto, ON, Canada).
X-Band spectra of semiquinones were recorded using a TM9103 resonator equipped with a temperature controller system (Bruker).
