During the incubation, the active transcription factor complexes in the sample were bound to their specific probes, whereas unbound probes were removed utilizing Marligen's patented digestion step.
Furthermore, the photoluminescence lifetime imaging at different oxygen levels exhibited that P1 is an excellent oxygen probe utilizing the sensitive phosphorescent lifetime to oxygen level.
When multiple probes were utilized, each probe was assembled separately and then mixed in SLO/medium just prior to delivery in equimolar concentrations.
Solvent-etching and fracturing were utilized for probing the interior lamellar textures of the blend samples.
Photoluminescence spectroscopy and fluorescence microscopy were utilized to probe the underlying photophysics of the perovskite film.
Solid-based spectroscopy techniques allowed identification of the chemical composition of the polymers, while gas sorption measurements were utilized to probe the microporosity, surface area, and pore size distribution of the constructed solids.
Polarization-dependent refractive indices were utilized to probe the free volume and anisotropic chain orientation of several types of microporous polyimides (PIs)/copolyimides (co-PIs) based on Tröger's base (TB).
These chemicals were utilized for probing accessibility of the reactive moieties upon changes in the protein structures due to unfolding, or intermolecular interactions.
The probes were further tested for possible partial cross hybridization and 56,163 probes were finally utilized for producing 105 K Agilent custom arrays.
A 10-MHz probe was utilized, and C-IMT was measured on both sides of the common carotid artery approximately 1.0 cm proximal to the carotid bulb.
