All IMN procedures reported in the five RCT were primary procedures.
RP-EC was prepared following the procedures reported in our previous paper (Ditta et al. 2015).
The graphene film was synthesized using the CVD method similar to procedures reported previously [21 23].
The jam development process was carried out according to standard procedures reported previously [34].
The authentic MMPIP was prepared according to procedures reported previously [11, 14].
However, most of the design procedures reported to date assume constant stream heat transfer coefficients.
Polymorphic tetranucleotide arrays in the PCR products were typed according to procedures reported previously.
Quinazoline derivatives 1 3 (Fig. 1b) were synthesized according to the procedures reported previously by our group [31, 32].
Finally, the in situ loading cycles procedure was critically compared with other in situ activation procedures reported in the literature.
The product was subjected to NaCl wash or Na+ pre-exchange following the procedures reported by Atkins et al. [15].
A monomer bearing a pendant mannose (p-acrylamidophenyl-α-D-mannoside [α-man]) was prepared via procedures reported previously [9].
