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Fig.2. Relationship between unsaturated and saturated1 in Characterization of the ovary fatty acids composition of Rhamdia quelen (Quoy & Gaimard) (Teleostei: Siluriformes), throughout their reproductive cycle
Fig.2. Relationship between unsaturated and saturated1fatty acids in Rhamdia quelen ovaries collected from natural environment and grouped according to their gonadal maturation stage. UFA/SFA = (monounsaturated fatty acids + polyunsaturated fatty acids)/ saturated fatty acids.
Figure 6. Caspase 3 in Physical characterization and wound healing properties of Zamzam water
Figure 6. Caspase 3 levels of treatment groups. ***Extremely high significant at p <0.001 when compared to Group 1; **Highly significant lesser at p <0.01 on comparing with Group 2; ns: nonsignificant when compared to group 3 at p <0.05. Group 1: Normal control; Group 2: Disease control (wound without treatment); Group 3: Standard control (treatment with povidoneiodine cream); Group 4: Zamzam water treatment group.
Figure 7. A comparative wound healing study. A1 in Physical characterization and wound healing properties of Zamzam water
Figure 7. A comparative wound healing study. A1: Control animals, dorsal view of wound soon after creating on the 1st day; B1: Dorsal view of the wound after treating with povidone-iodine cream on 3rd day; C1: Dorsal view of the wound after treating with Zamzam water on 3rd day; A2: Control animals, dorsal view of the wound on 6th day; B2: Dorsal view of the wound after treating with povidoneiodine cream on 6th day; C2: Dorsal view of the wound after treating with Zamzam water on 6th day; A3: Control animals, dorsal view of the wound on 12th day; B3: Dorsal view of the wound after treating with povidone-iodine cream on 12th day; C3: dorsal view of the wound after treating with Zamzam water on 12th day.
Figure 2. Serum IL-1 in Physical characterization and wound healing properties of Zamzam water
Figure 2. Serum IL-1β level of treatment groups. *Significantly lesser at p <0.05 on comparing with Group 2; **Highly significant lesser at p <0.01 on comparing with group 2; ns: nonsignificant when compared to Group 3. Group 1: Normal control; Group 2: Disease control (wound without treatment); Group 3: Standard control (treatment with povidone-iodine cream); Group 4: Zamzam water treatment group.
Figure 1 in Physical characterization and wound healing properties of Zamzam water
Figure 1. Zeta potential analysis of Zamzam water. (A) Before exposure to open-air; (B) After exposure to open-air.
Figure 3. Serum IL-6 in Physical characterization and wound healing properties of Zamzam water
Figure 3. Serum IL-6 level of treatment groups. ***Extremely high significant at p <0.001; **Extremely significant at p <0.01 on comparing with Group 2; ns: nonsignificant when compared to Group 3. Group 1: Normal control; Group 2: Disease control (wound without treatment); Group 3: Standard control (treatment with povidone iodine cream); Group 4: Zamzam water treatment group.
Figure 5. Caspase 9 in Physical characterization and wound healing properties of Zamzam water
Figure 5. Caspase 9 levels of treatment groups. ***Extremely high significant at p <0.001 when compared to Group 1; **Significantly lesser at p <0.01 on comparing with Group 2; ns: nonsignificant on comparing with group 3 at p <0.05. Group 1: Normal control; Group 2: Disease control (wound without treatment); Group 3: Standard control (treatment with povidone-iodine cream); Group 4: Zamzam water treatment group.
Figure 6 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 6. Photomicrographs of hepatocytes in control and experimental treated mice. Liver tissue sections stained with oil red O (×200) (A) and scored (B) by the semi-quantitative percentage of damaged area. (Control) control mice and (AEC) treated with C. gracilis extract (250 mg/kg) alone, showed normal structure. (HFD) high fed diet treated mice, showed a significant increase of lipid content; (AEC + HFD) co-treated with high fed diet and alga extract (250 mg/kg), representative micrograph revealed significantly reduced lipid liver content. Values are expressed as the mean ± SD. **p<0.01; ***p <0.001, indicates a significant difference compared to the control group. ++ p<0.01, indicates a significant difference compared to the HFD alone group.
Figure 3 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 3. Effect of ACE supplementation on plasma levels of inflammatory proteins. Data are given as mean ± SD for group of eight mice each. Values are statistically presented as follows: HFD and AEC-treated groups vs. control group: *p <0.05; **p<0.01. HFD + AEC group vs. HFD group: +p <0.05; ++p<0.01.
Figure 2 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 2. Antioxidant activity of different extracts of C. gracilis. Values are mean ± SD of three experimental tests, mg GAE/g DR: mg gallic acid equivalents per g dry residue. Table 4. Effect of AEC on body weight, liver and adipose tissues relative weight of control and treated mice groups.
Figure 5 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 5. Photographs of liver tissues in control and experimental treated mice. Liver tissue sections stained with hematoxylin and eosin (original magnification × 400). (A), in control mice showing normal histoarchitecture and radiating cell arrangement. (B) In mice treated with aqueous extract of C.gracilis (AEC) (250mg/kg) alone showing the normal liver structure. (C) In High fed diet (HFD) mice, representative photograph shows a significant lipid accumulation. (D) In group co-treated with HFD and AEC, was observed the reduction of fat accumulation.
Figure 1 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 1. Phenolic compounds of Cheatomorpha gracilis extract by chemical High Performance Liquid Chromatography (HPLC) analysis (gallic acid, Rutin, quercetin, Apegenin, kaempferol and Naringenin).
Figure 4 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 4. Effects of C.gracilis aqueous extract (AEC) on TBARS and protein carbonyls products (PCO) in HFD-treated mice. TBARS: thiobarbituric acid reactive substance. Data are presented as mean ± SD, n =8. *P≤ 0.05, **P≤ 0.01 compared with the control group. +P ≤0.05, ++P ≤0.01 as compared with HFD- treated mice.
Figure 5 in Escherichia coli expression and characterization of -amylase from Geobacillus thermodenitrificans DSM-465
Figure 5. The interaction of amylopectin (PubChem ID - 439207) and alpha-amylase enzyme active site. The left figure is built by Chimera and the right by MOE software.
Figure 4 in Escherichia coli expression and characterization of -amylase from Geobacillus thermodenitrificans DSM-465
Figure 4. Ramachandran plot for validation of alpha-amylase enzyme 3D structure generated by Raptor-X server.
Figure 3. 3 in Escherichia coli expression and characterization of -amylase from Geobacillus thermodenitrificans DSM-465
Figure 3. 3-dimentionsl protein structure of alpha-amylase built by Raptor-X software.α-helices are indicated by red, β-sheet by yellow and random coils by white. The protein structure consists of a single monomer.
Figure 2 in Escherichia coli expression and characterization of -amylase from Geobacillus thermodenitrificans DSM-465
Figure 2. Enzyme kinetics. (A) The effect of temperature on the enzyme stability; (B) determination of KM and Vmax values of purified alpha-amylase using Lineweaver-Burk plot; (C) The effect of reaction mixture temperature on the enzyme activity indicating an optimum temperature of 70°C; (D) The effect of pH on the enzyme activity, showing maximum activity at pH 8.
Figure 1 in Escherichia coli expression and characterization of -amylase from Geobacillus thermodenitrificans DSM-465
Figure 1. SDS-PAGE photograph indicating the expression and purification of alpha amylase. Lane C- control experiment (without gene), Lane-M. Protein marker (ThermoFisher Scientific PageRulerTM Prestained Protein Ladder, 10 kDa to 180 kDa), Lane E, experimental with expression of gene, Lane P, partially purified enzyme alpha amylase. The molecular weight of the purified enzyme was found as 63 kDa on SDS-PAGE.
Figure 2 in Phenotypic and molecular characterization of fluoroquinolone resistant Pseudomonas aeruginosa isolates in Palestine
Figure 2. Median-joining network of GyrA (A), ParC (B) and ParE (C) of the haplotypes of fluoroquinolone resistant P. aeruginosa isolates. Each haplotype is represented by a circle. The asterisk (*) denotes the founder haplotype. The size of circle is relative to haplotype frequency. Bars indicate the number of nucleotide substitutions for GyrA (A), ParC (B) and ParE (C) sequences from fluoroquinolone resistant P. aeruginosa isolates recovered in Palestine.
Figure 3 in Phenotypic and molecular characterization of fluoroquinolone resistant Pseudomonas aeruginosa isolates in Palestine
Figure 3. Nucleotide variation positions of GyrA (A), ParC (B) and ParE (C) genes among the studied fluoroquinolone resistant P. aeruginosa isolates according to the references from GenBank. Parsimony informative sites are shaded in light grey, while InDels are shaded in dark gray.
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.