S3 Table

Supporting Information to Accompany “Designing Two-Photon Fluorescent Probes Based on Target-Induced Enhancement of Absorption Cross Section”

(S3) Measurement of two-photon cross section. (S3) Cytotoxicity assay. (S3) Cell culture. (S4) Two-photon and one-photon fluorescence bioimaging. (S4) Calculation of mean fluorescence intensity (S4) Table S1. Absorption and emission maxima of 1a~1c in DMSO. (S4) Table S2. Absorption and emission maxima of 1c in various solvents. (S10) Fig. S10. 2P microscopy of 2a-labeled HeLa cells for biothio...

Correction: MoSET1 (Histone H3K4 Methyltransferase in Magnaporthe oryzae) Regulates Global Gene Expression during Infection-Related Morphogenesis

The gene list under the H3K4me2 column on the enriched_in_GT tab in S3 Table is incorrect. Please view the correct S3 Table below. S3 Table. List of genes differentially enriched for H3K4me2/me3 between mycelia and germtubes. access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provi...

Permutation Symmetry, Tri-Bimaximal Neutrino Mixing and the S3 Group Characters

We postulate that the neutrino mass matrix in the lepton flavour basis is an S3 group matrix in the natural representation of S3. This immediately requires one neutrino to be trimaximally mixed, as suggested by the solar neutrino data. We go on to postulate that the charged-lepton mass matrix in the neutrino massbasis is an S3 class matrix in the natural representation of the S3 class-algebra, ...

The IPEA dilemma in CASPT2† †Electronic supplementary information (ESI) available: Original data (Table S1) and additional comments for the literature survey; note on symmetry (Table S2), geometries (Table S3), data (Tables S4–S6) and comments (Section S2) for calculations on di-/triatomic molecules; results (Tables S7–S25) and comments (Section S3) for calculations on the organic molecular data set. See DOI: 10.1039/c6sc03759c Click here for additional data file.

S2 CASPT2/CASSCF vs. FCI Benchmark S20 S2.1 Computational Details . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . S20 S2.2 Closed-Shell vs. Open-Shell Characterization . . . . . . . . . . . . . . . . . . . S21 S2.3 Ground State Geometries of Diand Triatomic Molecules . . . . . . . . . . . . S23 S2.4 Excited State Energies of Diand Triatomic Molecules . . . . . . . . . . . . . . ...

High-level ab initio potential energy surface and dynamics of the F– + CH3I SN2 and proton-transfer reactions† †Electronic supplementary information (ESI) available: Benchmark classical and adiabatic relative energies (Table S1), vibrational frequencies of all the stationary points (Tables S2 and S3), direct/indirect trajectory separation function parameters (Table S4), entrance-channel potential (Fig. S1), structures of the minima and saddle points corresponding to the abstraction channel (Fig. S2), reaction probabilities (Fig. S3), trajectory integration time distributions (Fig. S4), trajectory integration time vs. I– velocity distributions (Fig. S5), and mechanism-specific reaction probabilities (Fig. S6). See DOI: 10.1039/c7sc00033b Click here for additional data file.

Direct cloning and refactoring of a silent lipopeptide biosynthetic gene cluster yields the potent antibiotic taromycin

1. Experimental methods 2. Strains and plasmids used in this study (Table S1) 3. Deduced functions and sequence comparison of the tar genes (Table S2) 4. Schematic diagram of the tar gene cluster direct cloning (Figure S1) 5. Restriction mapping of pCAP01-tar and its derivatives (Figure S2). 6. Results of heterologous expression of the tar gene cluster in S. coelicolor M1146 (Figure S3) 7. Resu...