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The method was successfully tested with human ubiquitin.
DHE and sumatriptan were tested with human 5-HT1B and 5-HT1D receptors in this study.
Future work will include a full design circle, where shared control will be optimized on measurements of neuromuscular control and tested with human experiments.
This method is tested with human recognition based on benchmark ear and face databases to verify the effectiveness and the advantages of the proposed method.
When tested with human whole blood in vitro, the FcMBL hemoadsorption filter (FcMBL-HF) produced efficient (90 99%) removal of Gram negative (Escherichia coli) and positive (Staphylococcus aureus) bacteria, fungi (Candida albicans) and lipopolysaccharide (LPS -endotoxin.
In this case the proposed method is tested with human recognition based on the face and ear biometric measures, where the proposed method aims at finding non-dominated solutions based on the number of data points for training and the recognition error.
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We went through a complete system development and evaluation cycle: designing the algorithms and interface for our prototype, implementing them and testing with human users.
The sensitivity and specificity of the newly developed multiplex RT-PCR method was evaluated by testing with human and porcine rotaviruses of known SG I, SG II, SG (I + II), and SG non-(I + II) strains in comparison with monoplex RT-PCR and VP6 sequence analysis.
Phosphate buffered saline was used as negative control and all positive samples were re-tested with human blood donor serum as negative control.
When genomic DNA from HeLa cells, Vero cells, and human N4124 was tested with the human 26plex the resulting repeats for the D6S1017 locus were (8, 8), (8, 9), and (11, 12), respectively.
Finally, the superhydrophobicity was tested with diluted human plasma, as preliminary step toward the use of micropillars for biomolecular detection in human samples.
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