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Figure 4 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 4. Putative cloverleaf secondary structures of the 22 tRNAs of P. eriobotryae. The dot "." indicated mismatched base pairs.
Figure 3 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 3. The ratios of nonsynonymous substitutions (Ka) and synonymous substitutions (Ks), and the ratio of Ka/Ks for each PCGs in the mitogenome of P. eriobotryae.
Figure 7 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 7. Phylogenetic tree of thrips obtained from Maximum-likelihood and MrBayes based on 13 PCGs dataset. The numbers on branches are superimposed with bootstrap support values (BP) and the Bayesian posterior probability (PP).
Figure 2 in Characterizing the complete mitochondrial genome of Psephenothrips eriobotryae Dang & Qiao (Thysanoptera: Phlaeothripidae) with massive gene arrangement in Phlaeothripidae
Figure 2. Codons distribution and usage in the mitogenome of P. eriobotryae. A. Amino acid composition: codon families are provided on the x-axis; numbers of codons of each amino acid are provided on the y-axis. B. The relative synonymous codon usage (RSCU).
Figure 4 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 4: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the COI gene sequence alignment under the GTR + I + G model. Posterior probabilities and bootstrap values ≥70% are given for appropriate clades. New sequences are indicated by bold font.
Figure 1 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 1: Photomicrographs of cysts, vulval cones, and J2 of P. stonei from Virginia. A, B: Anterior ends of J2s; C: Excretory pore and hemizonid with arrow pointing toward hemizonid; D, E: Entire cysts with D showing both fenestra in the middle; F: Cyst posterior part showing vulval and anal fenestrae; G: Lateral field with four incisures for J2; H, I: Tails of J2s with arrow pointing toward the anal area in I.J2, second-stage juveniles.
Figure 2 in First report of morphological and molecular characterization of Moroccan populations of Globodera pallida
Figure 2: Photomicrographs of morphological characterization of cyst, egg, and second-stage juvenile. A, B: Cyst of GlOBOdeRa pallida, C: Vulva (v), anus (a), and cuticular ridges (r) of cyst, D, E: Stylet knob shape of J2, F: Juvenile tail.
Figure 3 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 3: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the ITS rRNA gene sequence alignment under the GTR + I + G model. Posterior probabilities and bootstrap values ≥70% are given for appropriate clades. New sequences are indicated by bold font. *Identified as P. punctata in the GenBank and by Sabo et al. (2002).
Figure 1 in Molecular and morphological characterization of the alfalfa cyst nematode, Heterodera medicaginis, from Utah
Figure 1: Photomicrographs of second-stage juveniles (A-F) and vulva cones (G and H) of HeterOdera mediCaginiS. A-B heads; C-D tails; E-F lateral field; G-H cone mounts, G showing the bullae and H showing the underbridge. The scale bar=10 µm.
Figure 3 in First report of morphological and molecular characterization of Moroccan populations of Globodera pallida
Figure 3: Amplified PCR products from GlOBOdeRa Spp. digested by three enzymes AluI, MboI, and RsaI. A: Amplified PCR products, B: AluI, C: RsaI, D: MboI, MW: molecular weight markers (1 kb), NC: negative control, PC: undigested DNA, S1-S2: Eastern region samples, S3-S4: Western region samples (Gharb), S5-S6: Doukkala region samples.
Figure 2 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 2: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the D2–D3 of 28S rRNA gene sequence alignment under the GTR + I + G model. Posterior probabilities and bootstrap values ≥70% are given for appropriate clades. New sequences are indicated by bold font.
Figure 6 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 6. Localization of EtCHP18905 in infected DF-1 cells by indirect immunofluorescence. Parasites incubated with anti-rEtCHP18905, stained with FITC (green)-conjugated secondary antibodies, and counterstained with DAPI (blue). Infected DF-1 cells were collected at indicated time points post-infection. (A) Sporozoites (Spz) in PBS, pRB, posterior refractile body; (B) Spz in complete medium. Infected DF-1 cells were collected at the indicated time points post-infection (pi); (C) 2 hours pi (hpi); (D) immature schizonts (iSC) 48 hpi; (E) mature schizonts (mSC) 72 hpi; (F) merozoites (Mrz) in PBS.
Figure 3 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 3. Expression and purification of rEtCHP18905. (A) SDS-PAGE analysis of the 5rEtCHP18905. Lanes 1, protein marker; 2, negative control (not induced with IPTG); 3, the rEtCHP18905 protein with the GST-tag protein of the vector (induced with IPTG for 6 h). (B) Western blot analysis of purified rEtCHP18905 protein. Lane 2, protein recognized by an anti GST-Tag monoclonal antibody. (C) Western blot analysis of purified rEtCHP18905 protein. Lane 2, protein recognized by rabbit sera against sporozoite, lane 4 incubated with naïve rabbit serum.
Figure 2 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 2. Bioinformatic analysis of EtCHP18905. The stop codon is indicated with an asterisk. N-myristoylation sites are double underlined. The transmembrane domain is shaded yellow with black lettering. N-glycosylation sites are surrounded by a black box. cAMP- and cGMP-dependent protein kinase phosphorylation sites are shaded black with white lettering. Tyrosine kinase phosphorylation site is shaded grey with black lettering. Casein kinase II phosphorylation sites are indicated with red lettering. Protein kinase C phosphorylation sites are underlined by a wavy line.
Figure 1 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 1. Multiple alignment analysis of EtCHP18905 with other Eimeria proteins. DNAMAN was used to analyze the deduced protein sequences. The identical amino acids are listed at the bottom. NCBI reference sequence accession numbers: Eimeria tenella, XP_013231819, Eimeria necatrix, XP_013438465, Eimeria mitis, XP_013355934, Eimeria maxima, XP_013336337, Eimeria acervulina, XP_013251133; GenBank accession numbers: Eimeria praecox, CDI76926, Eimeria brunetti, CDJ52365.
Figure 7 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 7. Inhibition of sporozoite invasion in vitro by antirEtCHP18905. Anti-rEtCHP18905, rabbit anti-rEtCHP18905 IgG; NA, naïve rabbit sera IgG; GST control, rabbit anti-GST IgG. The symbol "*" represents p <0.05, "**" represents p <0.01, and "***" represents p <0.001 for comparison of treatment with antirEtCHP18905 and naïve rabbit sera IgG and anti-GST IgG at the same concentration. The error bars indicate the standard deviation. All assays were performed in triplicate.
Figure 4 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 4. Transcription levels of EtCHP18905 in different developmental stages of E. tenella. UO, unsporulated oocysts; SO, sporulated oocysts; Spz, sporozoites; Mrz, merozoites. Bars with different letters indicate significantly different expression levels (p <0.05) and the error bars indicate standard deviations.
Figure 5 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 5. Expression levels of EtCHP18905 in different developmental stages of E. tenella. (A) Western blot of the internal reference tubulin and EtCHP18905 protein. (B) Relative expression levels of the EtCHP18905 protein. Bars with different letters indicate significantly different expression levels (p <0.05) and the error bars indicate standard deviations.
Figure 8 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 8. Levels of IgG (A), sCD4 (B), sCD8 (C), cytokines IFN-γ (D), IL-10 (E), IL-17 (F) and TGF-β1 (G) in chicken sera were measured using ELISA. Chickens of group rEtCHP18905-50 μg and group rEtCHP18905-100 μg were immunized with 50 μg or 100 μg of rEtCHP18905 protein, respectively. Challenged and unchallenged groups were immunized with PBS and served as controls. The IgG titers and the concentrations of sCD4, sCD8, and cytokines are expressed as Min to Max. (*p <0.05, **p <0.01, ***p <0.001; ns, p> 0.05).
Figure 3. SDS PAGE and Western blots with rEnSerp1 in Identification and partial characterization of a novel serpin from Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)
Figure 3. SDS PAGE and Western blots with rEnSerp1, ESP and CWE. Lines 1–3, 1D gel. Lines 4–10, Western blot. M, protein standard; 1, rEnSerp1; 2, ESP; 3, CWE sample; 4, rEnSerp1 with anti-HIS antibodies; 5, rEnSerp1 without primary antibodies; 6, rEnSerp1 with anti-rEnSerp1 sera; 7, rEnSerp1 with pre-immune sera; 8, ESP with anti-rEnSerp1 sera; 9, ESP with pre-immune sera; 10, CWE with anti-rEnSerp1 sera. Arrow points to the expected recombinant EnSerp1 band. Arrowhead points to the natural form of EnSerp1 in the ESP sample. Dots indicate fragmented parts of rEnSerp1.
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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.