BUSCADOR RECOLECTA

All images show projections of confocal sections, except D, I, L, O, and Q, which show single confocal sections. (A, B) The overexpression of GFP-kkv in the trachea leads to the presence of intracellular chitin vesicles at early stages (pink arrowheads) (A, A’). At later stages, intracellular chitin vesicles are not present, and chitin is deposited extracellularly in the lumen (blue arrowheads and inset) (B, B’). (C, C’) In exp reb mutants, the overexpression of GFP-kkv in the trachea produces intracellular chitin punctae until late stages (pink arrowheads). (D) The overexpression of GFP-kkv in salivary glands produces intracellular chitin vesicles (pink arrowheads). (E) Schematic representation of Exp protein. (F, G) In exp reb mutants, the expression of a wild-type form of exp/reb rescues the lack of extracellular chitin deposition (F, white arrow and inset), while expΔMH2/rebΔMH2 do not (G, white arrow points to absence of CBP). (H, I) The co-overexpression of GFP-kkv and expΔMH2 in control embryo does not produce morphogenetic defects in trachea (H) or extracellular chitin deposition in salivary glands (white arrow) (I); however, intracellular chitin punctae are present (pink arrowheads in H, I, and inset in H). (J) The coexpression of GFP-kkv and expΔMH2 in exp reb mutants produces intracellular chitin particles (pink arrowheads) but does not rescue the lack of extracellular chitin deposition. (K, L) RebΔMH2 localises apically in trachea (K) and in salivary glands (L). (M) MH2-reb is not able to rescue the absence of extracellular chitin deposition in exp reb mutants. (N, O) The simultaneous expression of MH2-reb and GFP-kkv does not produce morphogenetic defects or ectopic chitin deposition in trachea (N) and in salivary glands (white arrow in O), but intracellular chitin vesicles are present (pink arrowhead in O). (P, Q) MH2-Exp protein does not localize apically in trachea (P) or in salivary gland (Q). Scale bars A-C, F-H, J, M, N: 25 μm; D, I, K, L, O-Q: 10 μm., Peer reviewed

The magnetoelectric phase diagram of A-site ordered REBaMn2O6 and A-site disordered RE0.5Ba0.5MnO3 perovskites studied in this investigation. Comparison between the X-ray diffraction patterns of the ordered REBaMn2O6 and disordered RE0.5Ba0.5MnO3 (RE: Sm and Y) samples at room temperature. Details about the experimental procedure to obtain k range extended EXAFS free of Nd and Sm self-absorption. Comparison of XANES spectra for the ordered YBaMn2O6 sample at 80 K recorded by Mn Kbeta-detected HERFD and conventional transmission modes., Peer reviewed

The excerpted portion of the immunoblot shown in the figures is highlighted by a black box., Peer reviewed

6 pages. -- S1. Optical characterization of the plasmonic biosensor. -- S2. Representative sensorgrams of antigen and virus detection assays. -- S3. SARS-CoV-2 virus detection with conventional SAM biofunctionalization. -- S4. Representative sensorgrams of neutralization assays with SARS-CoV-2 antigens. -- S5. Representative sensorgrams of neutralization assays with SARS-CoV-2 viruses., Peer reviewed

6 pages. -- Table S1: Description of various coatings developed for spray casting. -- Table S2: Theoretical density of materials for slurry preparation. -- Table S3: Specifications of electrodes. -- Figure S1: Gravimetric capacitance at different scan rates. -- Figure S2: Volumetric capacitance at different scan rates. -- Figure S3: Cyclic polarisations of different electrode materials at 10 mV s−1. -- Figure S4: Dependence of electrode gravimetric capacitance (at 10 mV s−1) on thickness and porosity. -- Figure S5: Dependence of electrode volumetric capacitance (at 10 mV s−1) on thickness and porosity. -- Figure S6: Gravimetric capacitance (at 10 mV s−1) of various electrodes as a function of thickness and mass. -- Figure S7: Volumetric capacitance (at 10 mV s−1) of various electrodes as a function of thickness and mass., Peer reviewed

Surface pressure decay vs time while barriers are stopped in cssc protocol Surface potential rise vs time during barriers are stopped in cssc protocol Model of the 2D Ni3(HHTP)2 planes UV-vis reflection spectra of the Ni3(HHTP)2 Langmuir film using the cc protocol AFM images of Cu foil substrate Cyclic Voltammetry at different v rates Estimation of b-value CV plots at 0.1 mVs-1 before and after cycling High resolution XPS spectra of C1s and O1s, Peer reviewed

19 pages. -- Characterization. -- Electrode preparation and electrochemical measurements. -- Theoretical method. -- Table S1. Complete list of samples produced and characterized, including name, precursors and processing conditions. -- Figures S1-S25. -- Table S2. Comparison of OER activity of obtained catalyst. -- Table S3. Cdl and ECSAs of various catalysts. -- Table S4. Simulated parameters from the relevant equivalent circuits. -- Table S5. OER activity of CoFexOy-SO4 and other Co-based catalysts in 1M KOH electrolyte., The electrochemical oxygen evolution reaction (OER) plays a fundamental role in several energy technologies, which performance and cost-effectiveness are in large part related to the used OER electrocatalyst. Herein, we detail the synthesis of cobalt-iron oxide nanosheets containing controlled amounts of well-anchored SO42– anionic groups (CoFexOy-SO4). We use a cobalt-based zeolitic imidazolate framework (ZIF-67) as the structural template and a cobalt source and Mohr’s salt ((NH4)2Fe(SO4)2·6H2O) as the source of iron and sulfate. When combining the ZIF-67 with ammonium iron sulfate, the protons produced by the ammonium ion hydrolysis (NH4+ + H2O = NH3·H2O + H+) etch the ZIF-67, dissociating its polyhedron structure, and form porous assemblies of two-dimensional nanostructures through a diffusion-controlled process. At the same time, iron ions partially replace cobalt within the structure, and SO42– ions are anchored on the material surface by exchange with organic ligands. As a result, ultrathin CoFexOy-SO4 nanosheets are obtained. The proposed synthetic procedure enables controlling the amount of Fe and SO4 ions and analyzing the effect of each element on the electrocatalytic activity. The optimized CoFexOy-SO4 material displays outstanding OER activity with a 10 mA cm–2 overpotential of 268 mV, a Tafel slope of 46.5 mV dec–1, and excellent stability during 62 h. This excellent performance is correlated to the material’s structural and chemical parameters. The assembled nanosheet structure is characterized by a large electrochemically active surface area, a high density of reaction sites, and fast electron transportation. Meanwhile, the introduction of iron increases the electrical conductivity of the catalysts and provides fast reaction sites with optimum bond energy and spin state for the adsorption of OER intermediates. The presence of sulfate ions at the catalyst surface modifies the electronic energy level of active sites, regulates the adsorption of intermediates to reduce the OER overpotential, and promotes the surface charge transfer, which accelerates the formation of oxygenated intermediates. Overall, the present work details the synthesis of a high-efficiency OER electrocatalyst and demonstrates the introduction of nonmetallic anionic groups as an excellent strategy to promote electrocatalytic activity in energy conversion technologies., Peer reviewed

Table of Contents for the Supporting Information Section S1. Discussion for the DPPC and CHOL isotherms and their mixtures Section S2. Discussion for the CCM stability at the air-water interface Section S3. Thermodynamic study of the binary mixtures Section S4. Thermodynamic study of the ternary mixtures at the air-water interface., Peer reviewed

(A) Projection of confocal sections of salivary glands shows that Kkv is normally expressed in salivary glands and accumulates apically. (B-D) Single confocal sections of trachea at early stages. Single chitin punctae do not colocalise with deacetylases or Gasp. (E, F) Single confocal sections of salivary glands expressing serp and verm. Single chitin punctae do not colocalise with deacetylases. (G) Frames from live imaging movie 2 show that common GFP-Kkv and chitin punctae (yellow arrow) can separate from each other; many GFP-Kkv (green arrow) and chitin puncta (red arrow) do not colocalise. (H) The luminal GFP-Kkv punctae are labelled by GFP and Kkv. Scale bars A, E, F: 5 μm; C-D, G: 10 μm., Peer reviewed

Table of contents: 1. Materials and Methods 2. Synthetic Schemes and Experimental Details of the Synthesis of Compounds. 3. NMR Spectra of Representative Compounds 4. Thermal and Liquid Crystal Properties of The Compounds. 5. X-ray diffraction studies, Peer reviewed