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Figure 3 in Identification and expression of Dmrt1 and Sox9 during the gonadal differentiation of Rana chensinensis
Figure 3. Nucleotides and deduced amino acids of rcSox9. The HMG-box domain is boxed in shaded rectangles, while the Sox-N domain and PQA-rich element are underlined with a solid and dotted line, respectively. The stop codon is marked by an asterisk.
Figure 3 in Validation of reference genes for quantitative expression analysis by qPCR in various tissues of date mussel (Lithophaga lithophaga)
Figure 3. Pairwise variation (V-value) of candidate reference genes in date mussel (L. lithophaga) using geNorm.
Figure 2 in The effects of feeding obese rats with bee bread on leptin and ghrelin expression
Figure 2. Cells stained with ghrelin (A) and leptin (B) in hypothalamus tissue are shown with black arrows. A: Group 1 (fed with standard rat food), B: Group 2 (obese - fed with high-fat diet), C: Group 3 (high-fat diet and 100 mg/kg/day bee bread), D: Group 4 (high-fat diet and 200 mg/kg/day bee bread), E: Group 5 (high-fat diet and 300 mg/kg/day metformin). Image zoom 400×.
Figure 1 in The effects of feeding obese rats with bee bread on leptin and ghrelin expression
Figure 1. Cells, stained with hematoxylin and eosin in hypothalamus tissue are shown with black arrows. Image zoom 400×. A: Group 1 (fed with standard rat food), B: Group 2 (obese - fed with high-fat diet), C: Group 3 (high-fat diet and 100 mg/kg/day bee bread), D: Group 4 (high-fat diet and 200 mg/kg/day bee bread), E: Group 5 (high-fat diet and 300 mg/kg/day metformin).
Figure 2 in Autophagic chemicals effect to Atg8 and rice stripe virus relative expressions, and Wolbachia relative density in Laodelphax striatellus (Hemiptera: Delphacidae)
Figure 2. Comparison of Atg8, Wolbachia, and RSV relative expressions and densities. Vertical bar lines indicate the ± of SD. Significant difference was determined by the Student's t-tests accompanied by Bonferroni correction (0.05). Control was used as a reference. Asterisks represent a significant difference in genes between treatment and control (*p <0.05).
Figure 1 in Autophagic chemicals effect to Atg8 and rice stripe virus relative expressions, and Wolbachia relative density in Laodelphax striatellus (Hemiptera: Delphacidae)
Figure 1. Comparison of Atg8, Wolbachia, and RSV relative expressions and densities. Vertical bar lines indicate the ± of SD. Significant difference was determined by the Student's t-tests accompanied by Bonferroni correction (0.05). Control was used as a reference. Asterisks represent a significant difference in genes between treatment and control (*p <0.05).
Fig. 1 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 1. Zymogram of midgut proteins from Trichoplusia ni with casein as substrate. (A) 6-12% Z Blue casein (substrate in gel), or (B) 4-16% Tricine gel, incubated in casein solution postelectrophoresis. Migration of molecular markers is indicated on the lef, and proposed T. ni protease numbering (P1 – P7) on right, based on migration in the gel.
Fig. 2 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 2. Zymogram of midgut proteins from Trichoplusia ni with either 2% Xen- Tari (A) or 1% Cry1Ac-HD73 (B) as substrate. GT and G represent the GTO strain. Migration of molecular markers is indicated on the lef, and proposed T. ni protease numbering (P1 – P7) on right, based on migration in the gel.
Fig. 4 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 4. Relative DNA detected by semi-quantitative RT-PCR using the imageJ sofware, comparing the tnapn1 versus the rs5 control transcript as amplification reference. Trichoplusia ni strains NLX, GTOX and USX represent NL, US and GTO afer 5 generations being exposed to XenTari.
Fig. 3 in Activity and expression of midgut proteases from Mexican and US Trichoplusia ni (Hübner) strains exposed to Bacillus thuringiensis
Fig. 3. Detection of protease activity in midgut extracts from different Trichoplusia ni strains using class-specific substrates. (A) N-a-benzolyl-L-arginine-pNA (BApNA) for detection of trypsin-like activity; (B) N-succinyl-ala-ala-pro-phepNA (SAAPFpNA) for detection of chymotrypsin-like activity; and (C) N-succinylala-ala-pro-leu-pNA (SAAPLpNA) for detection of elastase-like activity.
Figure 1 in The Combined Expression Patterns of Ikaros Isoforms Characterize Different Hematological Tumor Subtypes
Figure 1. - Location of sites cited in table I, where the new records were gathered. 1) San Jorge, 2) La Poma, 3) Punta del Diablo, 4) Patos Island, 5) El Chivero, 6) La Reina, 7) La Tordilla, 8) San Pedro Mártir.
Fig. 1. Differentially expressed genes between infected and uninfected P in Subtle transcriptomic response of Eurasian perch (Perca fluviatilis) associated with Triaenophorus nodulosus plerocercoid infection
Fig. 1. Differentially expressed genes between infected and uninfected P. fluviatilis in a) spleen and b) liver tissues. Filled-in and empty boxes on the top of each plot represent infected and uninfected individuals, respectively. N/A indicates unknown protein.
FIGURE 1 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 1 | Partial sequence of nucleotides and amino acids (AA) encoding glut2 (glucose transporter 2) from Petenia splendida taken from Gen Bank to design specific oligonucleotides for qPCR.
FIGURE 3 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 3 | Phylogenetic tree based on the sequence of glut2 (glucose transporter 2) from Petenia splendida and other teleosts using the neighbor-joining (NJ) method. Values at branch points represent percentage frequencies for tree topology after 1,000 interations.
FIGURE 4 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 4 | Relative expression of glut2 in kidney (K), liver (L), muscle (M), brain (B), pancreas (P), gill (G), heart (H), intestine (I), stomach (S) and testis (T) of adult Petenia splendida (mean ± SEM; n = 3). Lowercase letters indicate significant differences between the expression level in the tissues (p <0.05).
FIGURE 2 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 2 | Amino acid sequence of glut2 in Petenia splendida aligned with other species other species of teleost fish. Identical amino acids are presented in black, and the high and less conserved amino acids are presented in gray and period, respectively.
FIGURE 5 in Characterization and expression of the gene glucose transporter 2 (GLUT2) in embryonic, larval and adult Bay snook Petenia splendida (Cichliformes: Cichlidae)
FIGURE 5 | Relative expression of glut2 during the early ontogeny of Petenia splendida. Lowercase letters indicate significant differences in the expression of glut2 as a function of developmental time (p <0.05). AN: Artemia nauplii (3–10 dph), CF: cofeeding (Artemia nauplii and tilapia feed) (11–13 dph), TF: trout feed (14–30 dph) (mean ± SEM; n = 3).
Figure 2 in Expression analysis of phosphate induced genes in contrasting maize genotypes for phosphorus use efficiency
Figure 2. Phylogenetic analysis based on nucleotide sequences of plant phosphate transporters. Plant phosphate transporters were assembled using ClustalX, and NJ-plot was used to develop the tree. Abbreviations are shown for respective transporters: ZmPTs: Zea mays phosphate transporters;AtPT: Arabidopsis thaliana phosphate transporters;LePT: Lycopersicon esculentum phosphate transporters; OsPT: Oryza sativa phosphate transporters; HvPT: Hordeum vulgare phosphate transporters; SbPT: Sorghum bicolor phosphate transporters.
Figure 1. A – P in Expression analysis of phosphate induced genes in contrasting maize genotypes for phosphorus use efficiency
Figure 1. A – P-efficient and P-inefficient maize plants grown in the Cerrado under low Pi conditions.B – Dry weight of maize genotypes. C – Root/shoot ratio of maize plants. D and E – Phosphorus content. F – Anthocyanin concentration. G and H – Units of APA activity. B to H, The maize plants were grown in hydroponics culture in the presence (250 µM Pi - gray bar) or absence (0 µM Pi – black bar) of phosphate harvested after 15 days in treatment. Each bar is the mean of three replicates with a standard deviation.
Figure 3. A in Expression analysis of phosphate induced genes in contrasting maize genotypes for phosphorus use efficiency
Figure 3. A – Northern blot analysis of phosphate starvation-induced ZmPTs genes in maize genotypes. B – Expression of ZmPTs in a plant grown in different phosphorus concentrations. C – Suppression of the ZmPTs expression by Pi resupply. D – Expression of ZmPT genes using RNA isolated from different root parts. E – Expression of ZmPTs in different maize plants under Pi starvation. F – Effect of duration of phosphate starvation on ZmPTs genes expression in maize genotypes. G – Expression of ZmPT homologs in roots of two sorghum genotypes. Total RNA isolated from different times of hydroponically grown plants supplied with half-strength modified Hoagland's solution containing 250 µM phosphate (+) or no phosphate (-) for different days or different concentrations as indicated. All the blots were probed with 32P labeled ZmPTs. The panel below the Northern blots is the ethidium bromide-stained gel prior to blotting showing the RNA integrity and uniformity of loading.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.