The lowest energy span (ΔG = 28.7 kcal/mol) was identified for a neutral rhodium catalyst with E = C and X = NH in dichloromethane or tetrahydrofuran solution yielding a predicted TOF of 90 h−1 at 130 °C.
For PI-b-PFMMA with total molecular weight 13400 g/mol a phase transition at 105 °C was identified leading to the segmental mixing at T > 105 °C and microphase separation at T < 105 °C.
The apparent activation energies for ethanol (77.7 kJ/mol) and acetaldehyde (81.9 kJ/mol) formation suggested that both originated from the same surface intermediate whereas, a higher activation barrier was identified for methanol (114.5 kJ/mol).
The precursor of each novel miRNA was identified and could form a proper secondary hairpin structure with a maximal free energy of -18 kcal/mol.
Several glasses containing 5 mol% mixed alkali were identified in a strontium boro-galliosilicate compositional region for use at 850 °C.
Several studies have shown that glasses with 50 mol% P2O5 content are dominant in long chains or rings (i.e., Q species), whilst both Q and Q species have been identified for glasses with 45 mol% P2O5 [ 4, 28].
Laterally acquired DNA in bacteria can be identified by local anomalies in GC mol% content, and is often associated with IS elements or tRNA genes [ 52].
With X-ray diffraction (XRD), Transmission electron telescope (TEM), and absorption spectra (UV Vis), Cu0 NPs and Cu+ were identified in the glasses with low Cu concentrations (0.02; 0.04; 0.1 mol%), and Cu+ and Cu2+ were identified in the glasses with high Cu concentrations (0.2; 0.4; 0.6 mol%).
Such additional markers may be identified by WGS comparison of different isolates with the same commonly observed MOL-PCR profile.
Precursors of these novel miRNAs were identified and formed proper secondary hairpin structures, with free energies ranging from -26.91 kcal mol-1 to -132 kcal mol-1 (average of -52.54 kcal mol-1) (Table 2, Additional file 1).
Slm1 and Slm2 were identified originally as PP2B/calcineurin-binding proteins nearly contemporaneously in three different labs [Bultynck G et al. (2006) Mol. Cell. Biol. 26: 4729-4745; Tabuchi M et al. (2006) Mol. Cell. Biol. 26 : 5861 -5875; Daquinag A et al. (2007) Mol. Cell. Biol. 27: 633-650].
