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Fig. 3 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 3. Mass spectra of different types of Panax notoginseng samples analyzed by iEESI-MS. (a) Mass spectrum of Panax notoginseng from Kunming, (b) Mass spectrum of Panax notoginseng from Qujing, (c) Mass spectrum of Panax notoginseng from Hongjiaozhou, (d) Mass spectrum of Panax notoginseng from Wenshan (1 year), (e) Mass spectrum of Panax notoginseng from Wenshan (2 year), (f) Mass spectrum of Panax notoginseng from Wenshan (3 year), (g) Mass spectrum of Panax notoginseng from Hongjiaozhou (black soil), (h) Mass spectrum of Panax notoginseng from Hongjiaozhou (white soil), (i) Mass spectrum of Panax notoginseng from Hongjiaozhou (red soil). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 2. Chemical structures of eight ginsenosides used in this study as reference standards. G, ginsenoside; NG, notoginsenoside; glc, glucoside; rha, rhamnoside; xyl, xyloside; ara, arabinoside.
Fig. 1 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 1. Schematic illustration of iEESI-MS for direct analysis of Panax notoginseng samples. (a) Analytical procedure of Panax notoginseng analysis by iEESI-MS. Approximately 0.1 mg of Panax notoginseng tissue was loaded into the sample chamber by punching without sample pretreatment, (b) Disposable iEESI device and its components, (c) Photo of iEESI-MS interface.
Data and Codes of "A Pharmacological Representation-based LSTM Network for Drug–Drug Interaction Extraction"
<p>The datasets and source codes used and/or analyzed in study "A Pharmacological Representation-based LSTM Network for Drug–Drug Interaction Extraction".</p>
dataset for paper entitled "Effect of Moringa Oleifera Leaf Extract On Body Length, Malondialadehyd and Interleukin-6 Levels in Zebrafish Larvae (Danio Rerio) Induced Stunting Model with Rotenone"
<p>The dataset consist of:</p> <p>1. Appendices of tools and material used for laboratory research</p> <p>2. Certificate of ethical test </p> <p>3. Data of moringa oleifera controls</p> <p>4. Data of zebrafish growth </p>
Unlocking the genomes of formalin-fixed freshwater fish specimens: An assessment of factors influencing DNA extraction quantity and quality
<p>DNA quality and quantity metrics (Microsoft Excel worksheet with 3 sheets, one per species).</p> <p>We compared two protocols developed to extract DNA from formalin-fixed tissues using specimens of three freshwater fishes: Southern Brook Lamprey <em>Ichthyomyzon gagei</em>, Slimy Sculpin <em>Cottus cognatus</em>, and Brown Trout <em>Salmo trutta</em>. Extractions were attempted using hot alkali digestion with and without buffer wash pretreatments to compare the DNA concentration, purity, and fragment length of DNA recovered between extraction protocols, tissue types (muscle and caudal fin tissue for Brown Trout and Slimy Sculpin), and preservation periods (5 or 7 years for Southern Brook Lamprey).</p> <p>Four metrics were collected: DNA quantity (measured using Qubit 3.0 instrument with dsDNA high sensitivity kit); DNA purity measured by A260/A280 ratio (measured using NanoDrop 2000 spectrophotometer); DNA purity measured by A260/A230 ratio (measured using NanoDrop 2000 spectrophotometer); and percent fragments >= 300 base pairs (measured using ImageJ). For spectrophotometric absorbance ratios, an A260/A280 ratio of 1.8 and an A260/ A230 ratio of 2.0 were considered to represent “pure” DNA (i.e., free of contaminants). For analyses of DNA purity, deviations from 1.8 for the A260/A280 ratio and from 2.0 for the A260/A230 ratio were used as the response variables, such that larger deviation values corresponded to less-pure DNA.</p> <p>Please see attached README.md file for additional information.</p>
Master data of the article "Effect of ethanol extract of nigella sativa L seeds and propofol on BDNF protein level as neuroplasticity and neuroprotection of traumatic brain injury in rats"
<p><strong>Master data of the article "Effect of ethanol extract of nigella sativa L seeds and propofol on BDNF protein level as neuroplasticity and neuroprotection of traumatic brain injury in rats"</strong></p>
TransBic: extracting bucket trend-preserving biclusters for analysis of gene expression data
<p>Datasets of TransBic: extracting bucket trend-preserving biclusters for analysis of gene expression data</p>
Fig. 5 in Magnetic Ti C MXene functionalized with β-cyclodextrin as magnetic solid-phase extraction and in situ derivatization for determining 12 phytohormones in oilseeds by ultra-performance liquid chromatography-tandem mass spectrometry
Fig. 5. Spatio-temporal distribution of target phytohormones in different tissue of rapeseed germination.
Fig. 2 in Magnetic Ti C MXene functionalized with β-cyclodextrin as magnetic solid-phase extraction and in situ derivatization for determining 12 phytohormones in oilseeds by ultra-performance liquid chromatography-tandem mass spectrometry
Fig. 2. XRD spectrum (a), FI-TR pattern (b), Raman spectrum (c) of the composite material, and magnetization hysteresis loop of Fe3O4@Ti3C2@β-CD (d).
Fig. 1 in Magnetic Ti C MXene functionalized with β-cyclodextrin as magnetic solid-phase extraction and in situ derivatization for determining 12 phytohormones in oilseeds by ultra-performance liquid chromatography-tandem mass spectrometry
Fig. 1. Schematic of the synthetic route for Fe3O4@Ti3C2@β-CD and the sample pre-treatment procedure.
Fig. 4 in Magnetic Ti C MXene functionalized with β-cyclodextrin as magnetic solid-phase extraction and in situ derivatization for determining 12 phytohormones in oilseeds by ultra-performance liquid chromatography-tandem mass spectrometry
Fig. 4. Effects of different cleanup sorbents (a), effects of the amount of magnetic solid-phase extraction sorbents (b), effects of the simultaneous derivatization and magnetic solid phase extraction time (c), effects of the desorption time (d). 5 mg rapeseed spiked with 10 ng/g of each analyte.
Fig. 3 in Magnetic Ti C MXene functionalized with β-cyclodextrin as magnetic solid-phase extraction and in situ derivatization for determining 12 phytohormones in oilseeds by ultra-performance liquid chromatography-tandem mass spectrometry
Fig. 3. SEM image of Ti3C2 (a) and Fe3O4@Ti3C2@β-CD (b), TEM image of Ti3C2(c) and Fe3O4@Ti3C2@β-CD (d), elemental mapping and chemical composition of Fe3O4@Ti3C2@β-CD (e).
Fig. 3 in The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
Fig. 3. Heatmap and dendrogram based on Euclidean distance and Ward's clustering algorithm. FSG = fructose–sucrose–glucose; Glu_ChCl = glucose–choline chloride; Pro_Mal = proline–malic acid; Su_Ca = sucrose–citric acid.
Figure 1 in The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
Figure 1. Principal component analysis scores plot indicating the sample groupings of the different NaDES extracts. This analysis was based only on the putative phenolic compounds. FSG = fructose–sucrose–glucose; Glu_ChCl = glucose– choline chloride; Pro_Mal = proline–malic acid; Su_Ca = sucrose–citric acid.
Fig. 4 in The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
Fig. 4. PCA biplot of the anthocyanins determined by HPLC. FSG = fructose–sucrose–glucose; Glu_ChCl = glucose–choline chloride; Pro_Mal = proline–malic acid; Su_Ca = sucrose–citric acid.
Fig. 5 in The phenolic profile extracted from the desiccation-tolerant medicinal shrub Myrothamnus flabellifolia using Natural Deep Eutectic Solvents varies according to the solvation conditions
Fig. 5. Bar plots showing the concentrations of the anthocyanins detected using HPLC in the different NaDES extracts. Values are based on the mean of three replicates. The error bars represent the standard deviation.
Developing a Method to Automatically Extract Road Boundary and Linear Road Markings from MMS Point Cloud using OBB Collision Detection Techniques
<p>This video demonstrates the application of our method in a software tool for constructing road boundaries and lane marking data.</p>
dataset for paper entitled "Forty Six Years of Research about Extract of Plants as Herbal Medicine on Embryo of Zebrafish and Their Properties to Human "
<p>This is the dataset of list of papers related to use of plants on embryo of Zebrafish from 1977-2023 on Scopus website </p>
Comparison of leaves and stem Aq. extract of Tridax Procumbens for antimicrobial activity
<p>In present study, aq. extracts of leaves and stem part of Tridax Procumbens were compared for antimicrobial activity. Firstly, all organoleptic and physicochemical properties of leaves and stem powder were evaluated and it shows that drug is pure and having required constituents sufficiently. Aq. extract of leaves powder and stem powder was prepared separately using Soxhlet extraction technique. Both the extracts were evaluated for physiochemical screening using standard procedures. Aq. extract of leaves shows presence of tannis, saponins, anthocyanin, coumarins, alkaloids, proteins, amino acids, diterpenes, phytosterol, cardial glycosides, phlobatannins and flavonoids. Aq. extract of stem shows presence of tannins, coumarins, phenol, cardial glycosides and flavonoids. Both extracts were primarily evaluated for antimicrobial activity against E.coli and S. aureus by selecting dose of 500 mg. Finally, antimicrobial assay was performed for both extracts (500mg) against E.coli and S. aureus by well diffusion method using Amoxicillin and Amikacin as standards respectively. Antimicrobial assay shows that aq. extract of stem part is more effective against S. aureus than E.coli; leaves aq. extract also shows antimicrobial activity against S .aureus and E.coli. From present studies we can conclude that aq. extract of stem and leaves of Tridax Procumbens having antimicrobial activity and stem extract is more effective against S. aureus as compared to leaf extract</p>
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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.