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After ssDNA absorbed numerous methylene blue (MB), an ultrasensitive electrochemical readout was obtained.
The probe was inserted into the rectum up to 2 cm deep and held in the same position for 15 seconds until a stable temperature readout was obtained.
The readout was obtained by calculating the ratio of MCF-7 RLuc-MAP1LC3BWT/MCF-7 Rluc-MAP1LC3BG120A luminesceneighboringhboring wells exposed to the same treatment.
Confirmation on a cellular protein level of the results obtained using kinase inhibitors on the EGFR/AP-1 pathway in a cell-based reporter readout was obtained through immunocytochemistry.
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The readout is obtained from four readout channels with the linear encoding based on integrated resistors and the Center of Gravity approach.
For nucleic-acid-amplification the Amplified Tuberculosis Direct Test (Genprobe, San Diego, CA) was performed in duplicate according to the manufacturer's instructions (H37Rv served as a positive control and M. intracellulare served as the negative control) and readouts were obtained using a Leader 50 Luminometer (Genprobe, San Diego, CA).
After subtracting the polyclonals, low quality sequences, and nontemplated ISPs, 5-6 million final readouts were obtained from each run.
Reduced to only three injections, no measurable effect on the behavioral readout of hippocampal functions was obtained.
An experiment system was established and the sensitivity about −1.75 ppm/cm was obtained in the readout range of 1 20 cm.
The speed at which the animal became unable to stay on the drum was obtained and used as readout parameter.
Very good sensitivity was obtained in an electrical readout system using sheets of anti α-fetoprotein-functionalized graphene on a graphite electrode.
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