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505 results for “carriers”
Single-Carrier: Experimental Loop Recirculation Data Set - 250G
<p>Data set containing experimental results on the propagation of single-carrier optical signals over pure silica core fiber (PSCF) inside a recirculating loop. The net bit-rate is fixed at 250G (PM-16QAM).</p>
Single-Carrier: Experimental Loop Recirculation Data Set - 200G
<p>Data set containing experimental results on the propagation of single-carrier optical signals over pure silica core fiber (PSCF) inside a recirculating loop. The net bit-rate is fixed at 200G (PM-16QAM).</p>
Data used in article 'Tuning Charge Carrier Dynamics and Surface Passivation in Organolead Halide Perovskites with Capping Ligands and Metal Oxide Interfaces'
<p>Data underlying the article 'Tuning Charge Carrier Dynamics and Surface Passivation in Organolead Halide Perovskites with Capping Ligands and Metal Oxide Interfaces' published in Advanced Optical Materials.</p>
Dataset: Star Bulk Carriers Corp. (SBLK) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Figure 7 in Inflammation reduction potential of nanostructured lipid carriers encapsulated with rat's bone marrow cells' lysate
Figure 7. In-vivo Gene Expression Analysis: (A) represents apoptotic markers; BAX and Caspase-3, expression in treated nanostructured lipid carriers (T-NLC), treated bone marrow-derived mesenchymal stromal cells (BMSCs) lysate (C-I-BMSCs-L) and NLC loaded BMSCs lysate (C-I-NLC-BMSCs-L) groups as compared to normal (N) and carrageenan injected injury (C) groups (B) shows proinflammatory markers (IL-6 and IL-8) expression levels in treated C-I-BMSCs-L and treated C-I-NLC-BMSCs-L groups as compared to N and C groups (C) shows Proliferative markers (Ki-67, PCNA and TOP2A) expression in treated C-I-BMSCs-L and treated C-INLC-BMSCs-L group as compared to N and C groups. Whereas N-NS represents normal rats injected with normal saline, C-NS represents carrageenan-injected normal saline, C-I-DFS represents carrageenan-injected diclofenac sodium. Where; the* sign shows significance between untreated and treated groups while α and ss sign shows significance between carrageenan injury and other treatment groups. Where, ns is non-significant, * & α represents P<0.05, ** & ss represents P<0.001, *** & αss represents P<0.0001.
Figure 6 in Inflammation reduction potential of nanostructured lipid carriers encapsulated with rat's bone marrow cells' lysate
Figure 6. Percentage inhibition of inflammation at a time interval (hr) in carrageenan-induced rat's hind paw oedema model. The effect of different treatment groups, i.e., normal (N), normal rat paw injected with normal saline (N-NS), carrageenan injected group (C), carrageenan injected with normal saline group (C-NS), carrageenan injected with diclofenac sodium group (C-I-DFS), carrageenan injected with nanostructured lipid carriers group (C-I-NLC), carrageenan injected with bone marrow-derived mesenchymal stromal cells (BMSCs) lysate group (C-I-BMSCs-L) and Carrageenan injected with NLC loaded BMSCs lysate group (C-I-NLC-BMSCs-L); on hind paw oedema at different hours (0, 1 2, 3, 6 & 24 hours). Where; the* sign shows significance between normal and carrageenan-induced treated groups while α and ss sign shows significance between carrageenan injected and carrageenaninduced treatment groups. Where; ns is non-significant, ** & ss denotes P<0.001, *** & αss denotes P<0.0001.
Figure 4 in Inflammation reduction potential of nanostructured lipid carriers encapsulated with rat's bone marrow cells' lysate
Figure 4. (A) Expression analysis of angiogenesis marker vascular endothelial growth factor (VEGF) via immunocytochemistry; (B) Expression analysis of apoptotic marker p53 via immunocytochemistry; (C) Expression analysis of apoptotic marker p53 via immunocytochemistry. Where: Untreated (UT), H 2 O 2 injury (I-H 2 O 2), treated NLC (T-NLC), treated BMSCs lysate (T-BMSCs-L), and treated NLC loaded bone marrow-derived mesenchymal stromal cells lysate (T-NLC-BMSCs-L). Stained cells are red, and blue denotes the nuclei counterstained with 4′,6-diamidine-2′-phenylindole dihydrochloride (DAPI,) while arrows show the positive cells expressing the protein. Scale bar: 200µm.
Figure 2 in Inflammation reduction potential of nanostructured lipid carriers encapsulated with rat's bone marrow cells' lysate
Figure 2. Represents cytotoxicity analysis/percentage cell viability and standardized viability concentration (SVC) values of different treatment groups on NIH 3T3 Cells (A) Represents the percentage of NIH 3T3 cells viability treated with different concentrations of nanostructured lipid carriers (NLC), bone marrow-derived mesenchymal stromal cells lysate (BMSCs-L), and NLC loaded BMSCs lysate (NLC-BMSCs-L). N represents % age viability of normal cells that receive no treatment and no H 2O2 injury; (B) Cytotoxicity analysis of various concentrations (500µg/µL, 1mg/mL, 2mg/mL, and 3mg/mL) of BMSCs lysate (C) SVC of BMSCslysate on NIH 3T3 cells; (D) Cytotoxicity analysis of various concentrations (500µg/µL, 1mg/mL, 2mg/mL, and 3mg/mL) of NLC loaded BMSCs lysate (E) shows SVC of NLC loaded BMSCs lysate on cells. Where; ***P<0.0001, *shows significance between untreated and treated groups while α and ss sign shows significance between H 2O2 injury and other treatment groups, αss shows P<0.0001, and ns is non-significant.
Figure 1 in Inflammation reduction potential of nanostructured lipid carriers encapsulated with rat's bone marrow cells' lysate
Figure 1. (A) Scanning Electron Micrograph of NLC and (B) Scanning Electron Micrograph of NLC-BMSCs-L; (B) Characterization of nanostructured lipid carriers (NLC) loaded bone marrow-derived mesenchymal stromal cells (BMSCs) lysate via enzyme-linked immunosorbent assay (ELISA):vascular endothelial growth factor (VEGF) and interleukin-6 (IL-6) expression in NLC, BMSCs-L, and NLC loaded bone marrow-derived mesenchymal stromal cells lysate (NLC-BMSCs-L).Where; *P<0.05, **P<0.01, ***P<0.0001, ns is non-significant.
Data for article: Understanding the Visible-light Photocatalytic Activity of GaN:ZnO Solid Solution: the Role of Rh2-yCryO3 Cocatalyst and Charge Carrier Lifetimes Over Tens of Seconds
<p>Dataset underlying the publication 'Understanding the Visible-light Photocatalytic Activity of GaN:ZnO Solid Solution: the Role of Rh<sub>2-y</sub>Cr<sub>y</sub>O<sub>3</sub> Cocatalyst and Charge Carrier Lifetimes Over Tens of Seconds', published in Chemical Science (doi: 10.1039/C8SC02348D)</p>
example stimuli of "Behavioral effects of rhythm, carrier frequency and temporal cueing on the perception of sound sequences"
<p>Exemplary subset of stimuli accompanying the manuscript "Behavioral effects of rhythm, carrier frequency and temporal cueing on the perception of sound sequences"</p>
Fig. 1 in Investigations into the carrier-state of Theileria sp. (buffalo) in cattle
Fig. 1. Frequency distribution curves for Theileria parva and Theileria sp. (buffalo) positive animals. Indicated are frequency distribution plots of the CP values and the percentage observed in buffalo from National Parks, buffalo from the Bedrog ranch, and cattle from the Bedrog ranch sampled during the outbreak (3/12/2013) and monitored afterwards for T. parva (top panel) and T. sp. (buffalo) (bottom panel).
Fig. 2 in Investigations into the carrier-state of Theileria sp. (buffalo) in cattle
Fig. 2. Monitoring of Theileria parva and Theileria sp. (buffalo) positive animals over a period of 24 months. The gray shaded areas indicate CP values below the cutoff of the PCR assays. Stars indicate animals that were splenectomized and the arrow indicate the date of splenectomy. The cross indicates an animal that died of natural causes.
Fig. 3 in Carrier and vector of Pectobacterium carotovorum subsp. carotovorum and its handling through a base of entomopathogenic fungi in Agave sp.
Fig. 3. Massive growth of the Metarhizium anisopliae fungus on the Pectobacterium carotovora bacterium.
Fig. 2 in Carrier and vector of Pectobacterium carotovorum subsp. carotovorum and its handling through a base of entomopathogenic fungi in Agave sp.
Fig. 2. Countable growth of the Pectobacterium carotovora bacterium in a BD Bioxion cultivation medium (MacConkey agar).
Fig. 1 in Carrier and vector of Pectobacterium carotovorum subsp. carotovorum and its handling through a base of entomopathogenic fungi in Agave sp.
Fig. 1. (A) Growth of the Beauveria bassiana bacterium; (B) Growth of the Pectobacterium carotovorum bacterium.
The solute carrier superfamily interactome
<p><span>Solute carrier (SLC) transporters form a protein superfamily that enables</span><span> transmembrane transport of a wide range of substrates including nutrients, vitamins, </span><span>ions</span><span> and drugs</span><span>. There are about 450 different SLCs, </span><span>residing</span><span> in cellular and a variety of subcellular membranes, and playing a vital role in cellular homeostasis and metabolic regulation. Loss-of-function of an unusually high proportion of SLC transporters is genetically associated with a plethora of human diseases, making them a rapidly emerging but challenging drug target</span><span> class</span><span>. Knowledge of the protein environment of transporters </span><span>may elucidate </span><span>the molecular basis for their functional integration with</span> <span>metabolic and cellular pathways </span><span>and </span><span>help conceive pharmacological interventions based on modulating </span><span>proteostatic</span><span> regulations</span><span>,</span><span> including functional rest</span><span>o</span><span>ration. We aimed at obtaining a global survey of the SLC protein interaction landscape by using </span><span>a </span><span>robust</span><span>,</span><span> standardized</span><span>,</span><span> one-step </span><span>interaction proteomics</span><span> protocol. We mapped the protein-protein interactions of 396 SLCs, covering thousands of novel </span><span>relationships</span><span>, to be assessed individually in the future using transporter-specific assays. Network and clustering analysis allowed </span><span>identification of </span><span>proteins likely to affect the </span><span>proteostatic</span><span> regulation of transporters. We employed a streamlined functional assessment process based on RNA interference (RNAi)-genetic perturbation of cells and measurement of protein stability and localization, including some transport assays, to positively </span><span>validate</span><span> the functional role of over 50 </span><span>new </span><span>interactions. As an example, we</span> <span>d</span><span>etail</span><span> the role of a SLC16A6 phospho-degron in</span><span> the</span><span> recruitment of a SKP1-CUL1-F-box protein E3 ligase, and the contributions of PDZ-domain proteins LIN7C and MPP1 to the subcellular localization of SLC43A2. Overall, our work provides insights into the complex molecular network of membrane transporters while offering the largest </span><span>experimental mass spectrometry-derived </span><span>membrane protein data</span> <span>set</span> <span>to date as a resource for the scientific community.</span></p>
Original Data for Manuscript "Energy and Momentum Distribution of Surface Plasmon-induced Hot Carriers Isolated via Spatiotemporal Separation"
<p>Raw data of the time-dependent energy density calculation and time-resolved photoemission electron microscopy (TR-PEEM) measurements used in the manuscript.</p> <p>A preprint of the manuscript is available on arXiv: <a href="https://arxiv.org/abs/2107.14277">2107.14277</a></p> <p>The manuscript was published in <em>ACS Nano</em> 2021, 15, 12, 19559-19569 <a href="https://doi.org/10.1021/acsnano.1c06586">10.1021/acsnano.1c06586</a></p> <p>The data is provided in hdf5 files, which were produced using the snomtools python package (<a href="https://github.com/hartelt/snomtools">availale on github</a>) and can be read with any <a href="https://support.hdfgroup.org/HDF5/tools5desc.html">hdf5 compatible software</a>. The calculated data was produced as described in Ref.1 with the parameters given in the manuscript. For the experimental data, each zip file contains the raw data (hdf5 Files) as well as the PEEM settings used (sav Files as output from the experiment control software) for the respective measurement.</p> <p>Parts of the manuscript that are generated from the calculated data [calculation_energy_density.zip]:</p> <ul> <li>Figure 2 A</li> <li>Figure S2</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM real space dataset [PEEM_realspace.zip]:</p> <ul> <li>Figure 2 B</li> <li>Figure 3</li> <li>Figure S1</li> <li>Figure S3</li> <li>Figure S4</li> <li>Movie S2 [timeseries_binned_fermi.avi] in the supplementary material</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) SPP dataset [PEEM_k-space_timesteps_SPP.zip]:</p> <ul> <li>Figure 4 (in combination with the pump pulse reference dataset)</li> <li>Figure S5 B</li> <li>Figure S6 B</li> <li>Figure S7 B</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) pump pulse reference dataset [PEEM_k-space_timesteps_pump.zip]:</p> <ul> <li>Figure 4 (in combination with the SPP dataset)</li> <li>Figure S5 A</li> <li>Figure S6 A</li> <li>Figure S7 A</li> </ul> <p>Parts of the manuscript that are evaluated from the PEEM momentum space (momentum microscopy) data of the full timetrace, combining SPP dataset [PEEM_k-space_full-timetrace_SPP.zip] and pump pulse reference dataset [PEEM_k-space_full-timetrace_pump.zip]:</p> <ul> <li>Figure S8</li> </ul>
Figure 5 in First record of Poecilochirus mrciaki Mašán, 1999 (Acari, Parasitidae) and its phoretic carriers in the Iberian peninsula
Figure 5 Box plot of number of P. mrciaki per carrier [central line of box: median; box upper limit: upper quartile; box lower limit: lower quartile; outsiders are lower and upper extremes]. AST: Anoplotrupes stercorosus, CAL: Calliphoridae, CMA: Creophilus maxilosus, NLI: Necrodes littoralis, NVE: Nicrophorus vespilloides, TPY: Trypocopris pyrenaeus, DIP: unidentified Diptera.
Figure 2 Poecilochirus mrciaki deutonymph. A in First record of Poecilochirus mrciaki Mašán, 1999 (Acari, Parasitidae) and its phoretic carriers in the Iberian peninsula
Figure 2 Poecilochirus mrciaki deutonymph. A, ventral view (scale bar, 200 µm); B, tectum with irregular shape (scale bar, 10 µm); C, metapodal shield with a granulated surface (scale bar, 10 µm). Gn, gnathosoma; St, sternal plate; Op, opisthosoma; An, anal plate; CxII, coxa II; CxIII, coxa III.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.