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Immunoprecipitation of LAP-tagged Nanog protein in Nanog-LAP- and control wildtype ESCs identified well known interaction partners of Nanog including Nr0b1, Zfp281, Sall4, Nac1, Gdf3, Sox2 and Rnf2 and thus validated functionality of the Nanog-LAP ESC line (Table S5).
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In order to validate functionality of the simulators, two error criteria are considered: ideal- and constraint-based errors.
We have loaded, electrophoresed, and detected 108 to 1010 fluorescently labeled DNA molecules in a 25 capillary sub-array to validate functionality.
Transwell migration assays on Jurkat cells were used to validate functionality of the purified CXCL12.
Further investigations are required for validating functionality of these regions.
The inserted features are validated from functionality and manufacturing point of view.
We validated the functionality of the model and algorithm in several tests and comparisons with previously reported experimental data.
Measurements coupling on one hand SThM probe and the integrated RTD and, on the other hand, SThM probe with optical imaging, validated the functionality of the calibration chips.
The DNA biosensor contained two test lines which captured biotin and texas red labelled amplicons; a LAMP internal amplification control line that captured digoxigenin labelled amplicon; and a chromatography control line that validated the functionality of the conjugated gold nanoparticles and membrane.
Antibodies from patient samples on our SPR array were validated for functionality by interaction with the antigen immobilized on the sensor array.
In light of this, we proposed a multifunctional robotic end-effector capable of achieving the maintenance objective functions or goals of the robotic end-effector as shown in Fig. 2 and, thereafter, validated its functionality through a detailed system design evaluation and simulation.
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