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Figure 2 in Characterization of glutamine synthetase from the ammonium-excreting strain HM053 of Azospirillum brasilense
Figure 2. Western blot assays of glutamine synthetase after treatment with snake venom phosphodiesterase. Samples (~ 0.3 µg GS protein) were separated by SDS‐PAGE followed by Western blotting with an anti‐GS antibody. A) Wild-type glutamine synthetase; B) P347L glutamine synthetase. Lane 1: GS after 0 min of incubation at 30 ºC without any treatment; lanes 2 to 5: GS after 0, 10, 30 and 60 min incubation at 30 ºC with snake venom phosphodiesterase. Lane 6: GS after 60 min incubation at 30 ºC without treatment.
Fig. 7 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 7. Alignment of the predicted amino acid sequences of the CYP307A1 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. We detected a sense amino acid mutation (14-threonine to serine).. This figure is shown in color in a supplementary document online as Suppl. Fig. 7 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 5 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 5. Alignment of the predicted amino acid sequences of CYP307A1 in Panonychus citribetween the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Only one amino acid mutation (278-lysine to glutamine) was detected.. This figure is shown in color in a supplementary document online as Suppl. Fig. 5 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 6 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 6. Nucleotide sequence comparison of CYP381A2 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Just one SNP site was detected. The nucleotide transition of A to T was at position 40.. This figure is shown in color in a supplementary document online as Suppl. Fig. 6 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 4 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 4. Nucleotide sequence comparison of the CYP307A1 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Three SNP sites were detected in all. The first nucleotide mutation (A to C) is located at 841, the second mutation is 1395-T to C, and the final mutation is 1491-T to C.. This figure is shown in color in a supplementary document online as Suppl. Fig. 4 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 3 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 3. Quantitative Real-time PCR analysis of CYPs in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. The numbers of genes down-regulated and up-regulated in the RR relative to the SS are indicated above or below the X axis. The light or dark gray was susceptible strain and resistant strain, respectively.
Fig. 1 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 1. Number, family and clan distribution of cytochrome P450 genes in Panonychus citri. The number shown along each column represents the P450 family and the number in parenthesis is the number of individual genes in the corresponding family. The P450 gene sequence information generated is from the VectorBase of the P. citri transcriptome sequence.
Fig. 2 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 2. Neighbor-joining phylogenetic analysis of cytochrome P450 from Panonychus citri and Tetranychus urticae. 4clans were observed. There are species (P. citri and T. urticae) in the phylogenetic tree. Only 10 sequences belong to T. urticae; A (Pc) before the CYP name denotes P. citri, a (Tu) before the CYP name denotes T. urticae. Numbers at nodes are bootstrap values.
Fig. 2 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)
Fig. 2. General displacement of Anastrepha ludens SMR strain (solid line) and Tap-7 strain (broken line) in a Cartesian plane.
Fig. 1 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)
Fig. 1. Contours of displacement of the SMR strain (lef) and Tap-7 strain (right) of Anastrepha ludens inside the field plot. The density of the flies at each contour is indicated by the number.
Fig. 3 in Effects of a pathogenic Beauveria bassiana (Hypocreales: Cordycipitaceae) strain on detoxifying and protective enzyme activities in Xylotrechus rusticus (Coleoptera: Cerambycidae) larvae
Fig. 3. Effects of infection by Beauveria bassiana strain BbCC01 on protective enzyme activity in Xylotrechus rusticus larvae over time. A. Catalase (CAT). B. Peroxidase (POD). C. Superoxide dismutase (SOD). Data are expressed as mean ± SE (n = 3). Different letters indicate significant differences between means (P <0.05).
Fig. 4 in Effects of a pathogenic Beauveria bassiana (Hypocreales: Cordycipitaceae) strain on detoxifying and protective enzyme activities in Xylotrechus rusticus (Coleoptera: Cerambycidae) larvae
Fig. 4. Change of the protein content in Xylotrechus rusticus larvae infected with Beauveria bassiana strain BbCC01. Data are expressed as mean ± SE (n = 3). Different letters indicate significant differences between means (P <0.05).
Fig. 2 in Effects of a pathogenic Beauveria bassiana (Hypocreales: Cordycipitaceae) strain on detoxifying and protective enzyme activities in Xylotrechus rusticus (Coleoptera: Cerambycidae) larvae
Fig. 2. Effects of infection by Beauveria bassiana strain BbCC01 on detoxifying enzyme activity in Xylotrechus rusticus larvae over time. A. Carboxylesterase (CarE). B. Glutathione S-transferase (GST). C. Acetylesterase (AchE). Data are expressed as mean ± SE (n = 3). Different letters indicate significant differences between means (P <0.05).
Fig. 1 in Effect of Colombian strains of Steinernema colombiense (Rhabditida: Steinernematidae) and Heterorhabditis bacteriophora (Rhabditida: Heterorhabditidae) against Eurhizococcus colombianus (Hemiptera: Margarodidae) and Aeneolamia sp. (Hemiptera: Cercopidae)
Fig. 1. Percentage mortality (mean ± SE) of Aeneolamia sp. nymphs treated with Steinernema colombiense and Heterorhabditis bacteriophora strain Fresno at 12 d afer inoculation under greenhouse conditions. Different letters indicate significant differences (ANOVA and Tukey's HSD test at P <0.05).
Fig. 4 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 4. Production of mucilaginous colonies by Hirsutella citriformis Mexican strains under dark conditions. Mucilaginous colony produced by strain INIFAP- Hir-1 (lef) and colonies without mucilage in strain IB-Hir-1 (right), both afer 5 days of culture under dark conditions.
Fig. 1 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 1. Phylogenetic tree constructed with sequences of ITS1-5.8S-ITS2 of 19 Hirsutella species enlisted in the NCBI and 7 Mexican strains isolated from D. citri in Mexico. Percentages from bootstrap analysis that support branches in the tree are shown in the respective nodes. Scale represents the number of substitutions/100 nucleotides.
Fig. 5 in Mexican strains of Hirsutella isolated from Diaphorina citri (Hemiptera: Liviidae): Morphologic and molecular characterization
Fig. 5. Mortality of Diaphorina citri caused by Hirsutella citriformis blastospores. Values followed by the same letter did not differ statistically (Tukey; P = 0.05). Lines in the bars indicate SD.
Strain rate sensitivity of a Cu/Al2O3 multi-layered thin film
<p>AD: as deposited</p> <p>HT: heat treated</p> <p>Samples P01-16 : ~4.0 um wide pillars</p> <p>Samples P01-09 : ~2.9 um wide pillars</p> <p>Pillar dimensions and deformation properties are included in the Excel file. The supplied mechanical data is compliance and baseline (drift) corrected.</p>
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West) in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West)
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV in Morphological and molecular variability of Peridinium volzii Lemmerm. (Peridiniaceae, Dinophyceae) and its relevance for infraspecific taxonomy
◂Fig. 1 Morphology of thecate and coccoid cells, with labelled thecal plates. a–c, i, m Light microscopy, d–h, k–l scanning electron microscopy. a Ventral view of strain GeoM*788; b dorsal view of strain GeoM*793; c apical view of strain GeoK*044; d ventral view of strain GeoK*037; e dorsal view of strain GeoM*788; f apical view of strain GeoK*024, with the dehiscence of epithecal opening indicated by a blue line; g antapical view of strain GeoK*044; h leftlateral view of strain GeoM*866; i motile cell of strain GeoK*037; k–m coccoid cells showing variability in shape and size of strains k GeoM*866, l GeoM*793 and m GeoK*024. Abbreviations: n′: apical plate, n′′: precingular plate, n′′′: postcingular plate, n′′′′: antapical plate, na: anterior intercalary plate, nC: cingular plate, Sa: anterior sulcal plate, Sd: right sulcal plate, Sp: posterior sulcal plate. Ss: left sulcal plate. Scale bar: 10 µm. UA: 15 kV
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.