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.
6,383
datasets available to search
ShareScore release 0.9.0
Dataset results
6,383 results for “isolates”
FIGURE 3. Agerinia roselli from Les Saleres. IPS-82793, isolated right M1 in New dental material and redescription of Agerinia roselli (Primates, Adapiformes) from Les Saleres (early Eocene, NE Iberian Peninsula)
FIGURE 3. Agerinia roselli from Les Saleres. IPS-82793, isolated right M1 in occlusal (1), buccal (2) and lingual (3) views. IPS-82816, isolated right M1 in occlusal (4), buccal (5) and lingual (6) views. IPS-2542, left mandible fragment with M2 in occlusal (7), buccal (8) and lingual (9) views. IPS-82794, right mandible fragment with M2 in occlusal (10), buccal (11) and lingual (12) views. IPS-1981, holotype, left mandible fragment with M2 and M3 in occlusal (13), buccal (14) and lingual (15) views. IPS-2541, right mandible fragment with M2 and M3 in occlusal (16), buccal (17) and lingual (18) views. IPS-82795, right mandible fragment with M3 in occlusal (19), buccal (20) and lingual (21) views. IPS- 82790, left mandible fragment preserving part of the ramus mandibularis and a fragment of the M3 in occlusal (22), buccal (23) and lingual (24) views. Scale bar represents 3 mm.
FIGURE 4 in Methods for isolation and quantification of microfossil fish teeth and elasmobranch dermal denticles (ichthyoliths) from marine sediments
FIGURE 4. Examples of select taxonomically identifiable fossil ichthyoliths and modern counterparts. All modern ichthyoliths were isolated from specimens in the Scripps Marine Vertebrate Collection. The fossil Myctophidae and Triakidae specimens are from ODP Site 1262, and are 62 million years old. The Scaridae modern teeth are from Smithsonian National Museum of Natural History's Fish Collection and subfossil teeth are from coral reef sediment cores taken off of the coast of Bocas del Toro, Panama, and are approximately 1200 years old.
FIGURE 3. Paleocene-aged ichthyoliths from ODP Site 1262, stained with Alizarin Red S in Methods for isolation and quantification of microfossil fish teeth and elasmobranch dermal denticles (ichthyoliths) from marine sediments
FIGURE 3. Paleocene-aged ichthyoliths from ODP Site 1262, stained with Alizarin Red S. The scale bar is 500 μm, with teeth>106 μm in the upper row and teeth <106 μm in the lower. Note that in the coloring effect is present in all teeth, however, the degree of staining varies.
FIGURE 2. A flowchart showing the steps for sediment processing for efficient and effective ichthyolith isolation from a in Methods for isolation and quantification of microfossil fish teeth and elasmobranch dermal denticles (ichthyoliths) from marine sediments
FIGURE 2. A flowchart showing the steps for sediment processing for efficient and effective ichthyolith isolation from a variety of sediment types. Sediment types are in boxes, while processing steps are shown in ovals.
FIGURE 1 in Methods for isolation and quantification of microfossil fish teeth and elasmobranch dermal denticles (ichthyoliths) from marine sediments
FIGURE 1. An assortment of large (>106 μm fraction) denticles (elasmobranch scales; left) and fish teeth (right) from DSDP Site 596, a red clay core in the South Pacific. These ichthyoliths are approximately 52 million years old. Image was taken on the Hull Lab Imaging System, Yale University. Scale bar is 500 μm.
Figure 4 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 4. Enhancement of the root and shoot lengths of barley when inoculated with LCK121. *Indicates a significant effect (P value <0.05).
Figure 5 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 5. TEM micrograph of chitosan nanoparticles prepared by ionic gelation method. Table 3. Antimicrobial activity of silver nanoparticles (µl) with different concentrations against fungal and bacterial isolates.
Figure 1 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 1. Mean weight of healthy and infected fourth and fifth instar larvae of B. mori. Isolation and identification of bacterial isolates: Total of 7 bacterial were successfully isolated from the outer surface and the inner bоdy of silkworm larvae.
Figure 3 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 3. Enhancement of the root and shoot lengths of barley when inoculated with LCK121, A.LCK121-treated ones; B.control seedlings.
Figure 2 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 2. Evolutionary relationships of LCK121 and other related bacterial species as inferred using the neighbor-joining method.
Figure 5 in Isolation and characterization of Klebsiella oxytoca from the rhizosphere of Lotus corniculatus and its biostimulating features
Figure 5. Enhancement of the root and shoot dry weight of barley when inoculated with LCK121. *Indicates a significant effect (P value <0.05).
Figure 1 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 1 Molecular chemical structure of the substances 4-nerolidylcatechol (4-NC), isolated of Piper peltata, and catechol and nerolidol were obtained from Sigma-Aldrich®, used in larvicidal and cytotoxicity bioassays.
Figure 3 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 3 Frequency of anomalies in interphase nuclei. a – damage to Aedes aegypti neuroblasts exposed to 4-NC for two generations. b – data on Ae. aegypti oocytes exposed to 4-NC in G1.
Figure 2 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 2 Microphotographs of abnormalities in interphasic and metaphasic nuclei of neuroblasts and oocytes of Aedes aegypti, stained with Giemsa (pH 5.8) and lacto-acetic orcein (2%). Arrows indicate: a – normal interphasic nuclei of neuroblasts of the NC group, G 1; b and c – micronuclei in interphasic nuclei of neuroblasts of G 2 (40 and 60 µg/mL), respectively; d – budding and telophasic bridging nucleus of neuroblasts (60 µg/mL, G2); e – budding in interphasic nucleus of oocytes (40 µg/mL, G1); f – normal metaphasic chromosomes (NC, G1); g and h – chromosomal metaphases of neuroblasts showing achromatic secondary constriction (60 µg/mL, G2). Magnification: 1600×. Scale bar: 5 and 10 µm.
Genetic analysis of mycobacteria isolated from suspect bovine tuberculosis lesions in Wolaita, Ethiopia - code and datasets.
<p>Bovine tuberculosis (bTB), caused by Mycobacterium bovis and other members of the Mycobacterium tuberculosis complex (MTBC), is a significant concern for livestock and public health in Ethiopia. This study aimed to assess the prevalence and causative agents of bTB in cattle from four abattoirs in the Wolaita region of Ethiopia. </p>
Fig. 1 in Genetic identification and biological characterization of Baculovirus isolated from Helicoverpa armigera (Lepidoptera: Noctuidae) in Brazil
Fig. 1. Phylogenetic relationships among HearNPV isolates (BR1, BR2, BR3, Br4, and GEM) based on analysis of concatenated nucleotide sequences of the lef-8 and lef-9. The evolutionary history was inferred by using the Maximum Likelihood method. The tree with the highest log likelihood (−799.3699) is shown. The percentage of trees in which the associated taxa clustered together is shown next to the branches. Initial tree(s) for the heuristic search were obtained by applying the Neighbor-Joining method to a matrix of pairwise dis- tances estimated using the Maximum Composite Likelihood (MCL) approach. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 14 nucleotide sequences. All posi- tions containing gaps and missing data were eliminated.
Fig. 2 in Genetic identification and biological characterization of Baculovirus isolated from Helicoverpa armigera (Lepidoptera: Noctuidae) in Brazil
Fig. 2. Survival curves of Helicoverpa armigera (Lepidoptera: Noctuidae) afer feeding on corn leaves inoculated with 1 × 106 polyhedra per mL of baculovirus isolated. Gemstar®LC, BR1, BR2, BR3, BR4, and in control obtained with KaplanMeier estimator.
Fig. 4 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 4 RNA interference (RNAi) of CpCHSB in third-instar larvae (n = 200). a Expression levels of CpCHSB at 72 h after injecting siCHSB assessed by RT-qPCR. b siCHSB injection into third-instar reduces body length in fourth-instar larvae, as well as midgut length (c). d Percentage of pupation (x-axis) after egg-hatching. e Comparison of wing length in wild type (WT), negative control (NC) and siCHSB adults. f Number of follicles per ovary and the number of eggs per female mosquito (g) after injecting (n = 50) siCHSB. All surviving individuals were used for measurements, and results are shown as the mean ± SE (Student's t-tests: **P <0.01, ***P <0.001)
Figure 3 in Isolation and characterization of bacteria associated with silkworm gut under antibiotic-treated larval feeding
Figure 3. Phylogenetic relationship of bacterial strains isolated in this study with each other based on 16S rRNA gene sequence through Neighbor-Joining method using 1000 bootstrap replicates.
Figure 1 in Isolation and characterization of bacteria associated with silkworm gut under antibiotic-treated larval feeding
Figure 1. Amplification of 16S rRNA gene (1500 bp) of isolated bacterial strains; lane 1 = HG1, lane 2 = HG2, lane 3 = HG3, lane 4 = DG1, lane 5 = DG2, lane 6 = DG3, -ve = negative control, +ve = positive control, M = 1kb DNA marker.
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.