Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
324
datasets available to search
ShareScore release 0.9.0
Dataset results
324 results for “fluorescent imaging”
Fig. 7 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 7. (A) Fluorescence microscopy imaging of control (untreated cells (a), DPBA treated (b)) and treated with AE (c), CY (e) AE@DPBA (d), CY@DPBA (f) B16–F10 cells, for 24 h. The B16–F10 cells were stained for nuclei-DAPI (Blue), cytoskeleton-phalloidin Alexa 488 (Green), and AN@DPBA (Red), Scale bars, 20 and 10 μm. (B) Measurement of AN@DPBA complex fluorescence intensity in AE- and CY treated cells, compared to the free DPBA control. The results are expressed as means ± SD. Statistical analysis were performed by Student's t-test. (p-value ≤ 0.05 was considered statistically significant. ** (p <0.01); ns (non-significant)).
Fig. 2 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 2. (A) Proposed reaction route of DPBA complexing with cyanidin CY; (B) 1HNMR spectra at 400 MHz in D3COD for CY (blue), CY@DPBA complex (green), and DPBA (red). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 1. Fluorescence spectrometric analysis of (A) AN-rich chokeberry extract (AE) (black spectrum) and in the presence of DPBA (0.2%) (red spectrum), respective of (B) cyanidin-chloride standard (CY) free (black spectrum) and in the presence of DPBA (0.2%) (red spectrum). AE concentration: 9.2 μM, CY concentration: 92 μM. Excitation wavelength: 570 nm (A, B).
Fig. 6 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 6. (A) AN cytotoxicity in B16–F10 murine melanoma cells after 24 h of incubation with different concentrations of anthocyanin-extract (AE), determined with the WST-1 assay; (B) B16–F10 cells viability after 24 h of incubation with different concentrations of AE (9.2 μM), respective CY (92 μM) and their complexed forms with DPBA (0.2%).
Fig. 5 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 5. Representative chromatograms of the in-vitro metabolization and cellular absorption of cyanidin and cyanidin effects on the extract of AN obtained from chokeberry fruits, showing the identified compounds after 2 and 24 h of incubation with B16–F10 cells, in the cell culture medium. The main peaks are numbered according to Fig. 2A. Chromatograms were processed at 520 nm for cyanidin detection, and at 270 nm for cyanidin breakdown products. (A). AE 2 h, (B). AE 24 h, (C). CY 2 h, (D). CY 24 h.
Fig. 8 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 8. (A) Histograms showing the fluorescence intensity of cellular AE/CY@DPBA following 2 h and 24 h incubation time. (B) Fluorescence measurement of B16–F10 melanoma cells, incubated for 2 and 24 h with AE (9.2 μM) and CY (92 μM) complexed with DPBA dye (0.2%).
Fig. 4 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 4. HPLC/DAD/ESI+-MS total ion chromatograms of anthocyannins identified in the aqueous chokeberry extract (AE) and recorded at 520 nm: (A) m/z = 449, specific to Cy-3-gal and Cy-3-glu; (B) m/z = 419, characteristic for Cy-3- ara and Cy-3-xyl; and (C) m/z = 287, the CY aglycon fragment. For peak identification see Table 1.
Fig. 3 in Real-time fluorescence imaging of anthocyanins complexed with diphenylboric acid 2-aminoethyl inside B16-F10 melanoma cells
Fig. 3. Representative HPLC-DAD chromatograms of chokeberry AN containing extract (A) and the cyanidin chloride standard (B), recorded at 520 nm. Identified peaks at 520 nm correspond to (A): Cy-3-gal (peak 1), Cy-3-glu (peak 2), Cy-3-ara (peak 3), Cy-3-xyl (peak 4), and Cy (peak 5); (B). Cy-chloride.
Single-Cell Imaging Dataset: Hela FUCCI Cell Fluorescence Analysis
<p>Hela FUCCI Cell Dataset: Fluorescence Intensity and Segmentation</p> <p>The "Hela FUCCI Cell Dataset" is a comprehensive collection of fluorescence microscopy data capturing the fluorescence intensity of Hela FUCCI cells. The dataset encompasses a diverse range of cellular images acquired through fluorescence imaging techniques, offering valuable insights into the cellular behavior and fluorescent signal patterns.</p> <p>Contents:</p> <p>Fluorescence Intensity Data: The dataset includes fluorescence images of Hela FUCCI cells captured in both red and green channels. These images represent the intensity levels of cellular fluorescence signals.</p> <p>Purpose:<br> The dataset serves as a resource for researchers and scientists interested in cellular fluorescence analysis. It supports investigations into cellular dynamics, cell cycle studies, and fluorescence signal patterns. Researchers can utilize this dataset to develop and evaluate image processing, analysis, and machine learning techniques for cell detection and fluorescence quantification.</p> <p>Data Collection:<br> The data were collected using fluorescence microscopy techniques, capturing the distinct fluorescence signals emitted by Hela FUCCI cells. </p> <p>Usage:<br> Researchers can use this dataset to:</p> <p>Investigate fluorescence patterns and intensities of Hela FUCCI cells.<br> Develop and validate machine learning algorithms for cell segmentation and detection.<br> Explore cellular behaviors and dynamics under various experimental conditions.</p> <p>Citation:<br> If you use this dataset in your research, please cite the original source to acknowledge its contribution.</p> <p>Access and Availability:<br> The dataset is openly available through Zendo, accessible via the following link: https://zenodo.org/. Researchers are encouraged to explore, analyze, and contribute to the dataset's applications and advancements in cellular fluorescence analysis.</p>
The Value of Lymph Node Dissection of Indocyanine Green-guided Near-infrared Fluorescent Imaging in Esophagectomy
ClinicalTrials.gov study NCT04615806. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Precision Thyroid Cancer Surgery With Molecular Fluorescent Guided Imaging
ClinicalTrials.gov study NCT03470259. IPD Sharing: NO. Countries: 1. Publications: 2.
Fluorescence Imaging With Indocyanine Green(ICG) in Endoscopic Spinal Surgery
ClinicalTrials.gov study NCT05808140. IPD Sharing: Not stated. Countries: 1. Publications: 7.
Laser Speckle Contrast Imaging, Surgical Eye & ICG Fluorescence Imaging for Perfusion Assessment of the Gastric Conduit
ClinicalTrials.gov study NCT05685862. IPD Sharing: UNDECIDED. Countries: 1. Publications: 19.
Targeted Fluorescence Imaging in AMD
ClinicalTrials.gov study NCT05262244. IPD Sharing: NO. Countries: 1. Publications: 0.
Fibered Confocal Fluorescence Microscopy Imaging in Patients With Diffuse Parenchymal Lung Diseases
ClinicalTrials.gov study NCT01624753. IPD Sharing: Not stated. Countries: 1. Publications: 4.
ICG-based Fluorescence Imaging in Localization of Prostate Cancer and Metastatic Lymph Nodes
ClinicalTrials.gov study NCT02840617. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Fluorescence Image-Guided Lymphadenectomy in Robotic Gastrectomy
ClinicalTrials.gov study NCT03931044. IPD Sharing: Not stated. Countries: 1. Publications: 12.
Accuracy of Indocyanine Green (ICG) Fluorescence Imaging in Tenosynovial Giant Cell Tumor Surgery
ClinicalTrials.gov study NCT07315841. IPD Sharing: NO. Countries: 1. Publications: 10.
Near-Infrared Fluorescence Imaging With Indocyanine Green to Evaluate Bowel Anastomoses in Gynecologic Oncology Surgery
ClinicalTrials.gov study NCT06871787. IPD Sharing: UNDECIDED. Countries: 1. Publications: 7.
NIR Fluorescence Imaging Technique in Thoracic Surgery With ICG
ClinicalTrials.gov study NCT02611245. IPD Sharing: Not stated. Countries: 1. Publications: 4.
ScienceDex guides
Understand access before you commit
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.