Dried samples were reconstituted with the mobile phase and.
All three vials were identical in appearance and were reconstituted with 1 ml saline solution (0.9%).
ENPs were reconstituted with filtered L1 medium (Sigma, MO, USA) before being tested.
The dried, clean extracts were reconstituted with 0.5 ml BUBE (I.S).
NCPs containing the various FRET pairs were reconstituted with the 601 DNA positioning element.
Finally, anti-IgG-labeled MPs were reconstituted with 10 mL of PBS and divided into aliquots of 1 mL each.
Prior to selection, during in vitro evolution, they were reconstituted with buffer and served as the molecular baits.
Prior to selection, during in vitro evolution, they were reconstituted with buffer and served as the baits.
HeminD1 and HeminD2 were reconstituted with apo-HRP successfully to produce the two novel HRPs, rHRP1 and rHRP2, respectively.
The concentrated samples were reconstituted with 80% methanol (5 mL) and filtered through a 0.22-μm membrane syringe filter (CHOICE 13 mm, PTFE, Thermo Scientific, Waltham, MA, USA).
The extracted lipids were reconstituted with 200 µL chloroform and loaded to a pre-conditioned SPE cartridge (500 mg silica, 6 mL, Thermo Scientific).
