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Cluster grouping of Lablab <t>purpureus</t> (L.) Sweet, based on (A) pod length and (B) pod width were done using <t>SPSS</t> (version 16.0) for windows program. The clustering showed quite variation in pod length whereas not much variation in pod width. Variety no (1) to (14) represents different varieties such as AS-PCA-Lp (1); AS-PCA-Lp (2); AS-PCA-Lp (3); AS-PCA-Lp (4); AS-PCA-Lp (5); AS-PCA-Lp (6); AS-PCA-Lp (7); AS-PCA-Lp (8); AS-PCA-Lp (9); AS-PCA-Lp (10); AS-PCA-Lp (11); AS-PCA-Lp (12); AS-PCA-Lp (13); and AS-PCA-Lp (14). These varieties were collected from diverse habitat such as kitchen garden/backyard garden, road side, pond side, disturbed side and other geographical areas of Eastern Uttar Pradesh and field gene bank of these varieties is maintained at Rajgarh block of Mirzapur District of Eastern Uttar Pradesh, India.
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1) Product Images from "Varietal dataset of nutritionally important Lablab purpureus (L.) Sweet from Eastern Uttar Pradesh, India"

Article Title: Varietal dataset of nutritionally important Lablab purpureus (L.) Sweet from Eastern Uttar Pradesh, India

Journal: Data in Brief

doi: 10.1016/j.dib.2019.103935

Cluster grouping of Lablab purpureus (L.) Sweet, based on (A) pod length and (B) pod width were done using SPSS (version 16.0) for windows program. The clustering showed quite variation in pod length whereas not much variation in pod width. Variety no (1) to (14) represents different varieties such as AS-PCA-Lp (1); AS-PCA-Lp (2); AS-PCA-Lp (3); AS-PCA-Lp (4); AS-PCA-Lp (5); AS-PCA-Lp (6); AS-PCA-Lp (7); AS-PCA-Lp (8); AS-PCA-Lp (9); AS-PCA-Lp (10); AS-PCA-Lp (11); AS-PCA-Lp (12); AS-PCA-Lp (13); and AS-PCA-Lp (14). These varieties were collected from diverse habitat such as kitchen garden/backyard garden, road side, pond side, disturbed side and other geographical areas of Eastern Uttar Pradesh and field gene bank of these varieties is maintained at Rajgarh block of Mirzapur District of Eastern Uttar Pradesh, India.
Figure Legend Snippet: Cluster grouping of Lablab purpureus (L.) Sweet, based on (A) pod length and (B) pod width were done using SPSS (version 16.0) for windows program. The clustering showed quite variation in pod length whereas not much variation in pod width. Variety no (1) to (14) represents different varieties such as AS-PCA-Lp (1); AS-PCA-Lp (2); AS-PCA-Lp (3); AS-PCA-Lp (4); AS-PCA-Lp (5); AS-PCA-Lp (6); AS-PCA-Lp (7); AS-PCA-Lp (8); AS-PCA-Lp (9); AS-PCA-Lp (10); AS-PCA-Lp (11); AS-PCA-Lp (12); AS-PCA-Lp (13); and AS-PCA-Lp (14). These varieties were collected from diverse habitat such as kitchen garden/backyard garden, road side, pond side, disturbed side and other geographical areas of Eastern Uttar Pradesh and field gene bank of these varieties is maintained at Rajgarh block of Mirzapur District of Eastern Uttar Pradesh, India.

Techniques Used: Blocking Assay

2) Product Images from "Bacillus subtilis Produces Amino Acids to Stimulate Protein Synthesis in Ruminal Tissue Explants via the Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Beta–Serine/Threonine Kinase–Mammalian Target of Rapamycin Complex 1 Pathway"

Article Title: Bacillus subtilis Produces Amino Acids to Stimulate Protein Synthesis in Ruminal Tissue Explants via the Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Beta–Serine/Threonine Kinase–Mammalian Target of Rapamycin Complex 1 Pathway

Journal: Frontiers in Veterinary Science

doi: 10.3389/fvets.2022.852321

Expression of proteins (A) and genes (B) in the rumen explants with living and inactivated bacteria ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyse the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p
Figure Legend Snippet: Expression of proteins (A) and genes (B) in the rumen explants with living and inactivated bacteria ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyse the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p

Techniques Used: Expressing, Software

Protein expression with adding inhibitor LY294002 (A) and Rapamycin (B) in tissue culture ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. **Indicates highly significant difference ( p
Figure Legend Snippet: Protein expression with adding inhibitor LY294002 (A) and Rapamycin (B) in tissue culture ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. **Indicates highly significant difference ( p

Techniques Used: Expressing, Software

Effects of different concentrations of living bacteria Bacillus subtilis IIIVE-4 (A) and inactivated bacteria Bacillus subtilis IIIVE-4 (B) on protein expressions in the PIK3CB-AKT-mTORC1 pathway in rumen explants ( n = 9). The protective mechanism of 2.0 × 10 7 cfu/ml B. subtilis can promote protein synthesis in rumen explants by the PIK3CB-AKT-mTORC1 pathway. In the rumen of Holstein cows, 2.0 × 10 7 cfu/ml B. subtilis IIIVE-4 was able to secrete nutrients (methionine, leucine, etc.) to enhance protein synthesis by acting on the PIK3CB-AKT-mTORC1 signaling pathway and increasing the expression levels of 4EBP1 and P70S6K proteins. The expression of PIK3CB, p70s6k, AKT, and 4EBP1 proteins was highest when adding live IIIVE-4 bacteria at a concentration gradient of 10 7 cfu/ml, while mTOR proteins reached their highest expression at 10 8 cfu/ml and PDCD4 at 10 6 cfu/ml, but P70S6k and 4EBP1, which are more closely related to protein synthesis, reached their highest at a concentration gradient of 2.0 × 10 7 cfu/ml, so 2.0 × 10 7 cfu/ml was determined as the optimal bacterial solution concentration. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p
Figure Legend Snippet: Effects of different concentrations of living bacteria Bacillus subtilis IIIVE-4 (A) and inactivated bacteria Bacillus subtilis IIIVE-4 (B) on protein expressions in the PIK3CB-AKT-mTORC1 pathway in rumen explants ( n = 9). The protective mechanism of 2.0 × 10 7 cfu/ml B. subtilis can promote protein synthesis in rumen explants by the PIK3CB-AKT-mTORC1 pathway. In the rumen of Holstein cows, 2.0 × 10 7 cfu/ml B. subtilis IIIVE-4 was able to secrete nutrients (methionine, leucine, etc.) to enhance protein synthesis by acting on the PIK3CB-AKT-mTORC1 signaling pathway and increasing the expression levels of 4EBP1 and P70S6K proteins. The expression of PIK3CB, p70s6k, AKT, and 4EBP1 proteins was highest when adding live IIIVE-4 bacteria at a concentration gradient of 10 7 cfu/ml, while mTOR proteins reached their highest expression at 10 8 cfu/ml and PDCD4 at 10 6 cfu/ml, but P70S6k and 4EBP1, which are more closely related to protein synthesis, reached their highest at a concentration gradient of 2.0 × 10 7 cfu/ml, so 2.0 × 10 7 cfu/ml was determined as the optimal bacterial solution concentration. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p

Techniques Used: Expressing, Concentration Assay, Software

Expression of proteins (A) and genes (B) in the rumen explants with supernatant of inactivated bacteria ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyse the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p
Figure Legend Snippet: Expression of proteins (A) and genes (B) in the rumen explants with supernatant of inactivated bacteria ( n = 9). One-way ANOVA in SPSS 22.0 software was used to analyse the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p

Techniques Used: Expressing, Software

The relative expression of CDH1 mRNA at different culture times ( n = 9). CDH1 expression in rumen explants was measured to determine the activity of rumen explants in different culture media and different culture times and to further determine the optimal culture time and medium for the explants. The expression of CDH1 was stable rising before 12 h but decreasing after 16 h and remaining at a low expression level till the cultured end at 72 h. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. # Indicates significant difference compared to other groups at the same time or the same concentration gradient ( p
Figure Legend Snippet: The relative expression of CDH1 mRNA at different culture times ( n = 9). CDH1 expression in rumen explants was measured to determine the activity of rumen explants in different culture media and different culture times and to further determine the optimal culture time and medium for the explants. The expression of CDH1 was stable rising before 12 h but decreasing after 16 h and remaining at a low expression level till the cultured end at 72 h. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. # Indicates significant difference compared to other groups at the same time or the same concentration gradient ( p

Techniques Used: Expressing, Activity Assay, Cell Culture, Software, Concentration Assay

Effects of different concentrations of living IIIVE-4 bacteria on gene expression of key factors in the PIK3CB-AKT-mTORC1 pathway in rumen explants ( n = 9). The expression of 4EBP1 (A) , AKT (B) , mTOR4 (C) , P70S6K (D) , and PI3K (F) genes was highest when adding living IIIVE-4 bacteria at a concentration of 10 7 , while PDCD (E) gene expression was lowest when the bacterial concentration was 10 7 . One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p
Figure Legend Snippet: Effects of different concentrations of living IIIVE-4 bacteria on gene expression of key factors in the PIK3CB-AKT-mTORC1 pathway in rumen explants ( n = 9). The expression of 4EBP1 (A) , AKT (B) , mTOR4 (C) , P70S6K (D) , and PI3K (F) genes was highest when adding living IIIVE-4 bacteria at a concentration of 10 7 , while PDCD (E) gene expression was lowest when the bacterial concentration was 10 7 . One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd. The ratio of all gene expression levels compared to the housekeeping gene β-actin was obtained as the relative expression of the gene. *Indicates significant difference from control group within the same group ( p

Techniques Used: Expressing, Concentration Assay, Software

Effect of LY294002 and Rapamycin on the cell activity of rumen explants was determined by MTT. The MTT data indicated that the addition of LY294002 or Rapamycin did not affect viability or had toxic effects on rumen explants. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd.
Figure Legend Snippet: Effect of LY294002 and Rapamycin on the cell activity of rumen explants was determined by MTT. The MTT data indicated that the addition of LY294002 or Rapamycin did not affect viability or had toxic effects on rumen explants. One-way ANOVA in SPSS 22.0 software was used to analyze the data, presented as mean ± sd.

Techniques Used: Activity Assay, MTT Assay, Software

3) Product Images from "Identification and Characterization of Seven Glutathione S-Transferase Genes from Citrus Red Mite, Panonychus citri (McGregor)"

Article Title: Identification and Characterization of Seven Glutathione S-Transferase Genes from Citrus Red Mite, Panonychus citri (McGregor)

Journal: International Journal of Molecular Sciences

doi: 10.3390/ijms141224255

Developmental stage-specific expression patterns of the seven GST genes in Panonychus citri were evaluated using RT-qPCR. The following life stages were analyzed: egg, larvae, nymph and adult. The mRNA levels are expressed as mean fold transcription relative to egg. The letters above bars show significant differences among different developmental stages. The GAPDH gene was used as a reference. The differences among the four developmental stages were analyzed by one-way analysis of variance (ANOVA), followed by Duncan’s multiple range tests in SPSS 16.0 (SPSS Inc, Chicago, IL, USA).
Figure Legend Snippet: Developmental stage-specific expression patterns of the seven GST genes in Panonychus citri were evaluated using RT-qPCR. The following life stages were analyzed: egg, larvae, nymph and adult. The mRNA levels are expressed as mean fold transcription relative to egg. The letters above bars show significant differences among different developmental stages. The GAPDH gene was used as a reference. The differences among the four developmental stages were analyzed by one-way analysis of variance (ANOVA), followed by Duncan’s multiple range tests in SPSS 16.0 (SPSS Inc, Chicago, IL, USA).

Techniques Used: Expressing, Quantitative RT-PCR

4) Product Images from "Effect of Coconut Protein and Xanthan Gum, Soybean Polysaccharide and Gelatin Interactions in Oil-Water Interface"

Article Title: Effect of Coconut Protein and Xanthan Gum, Soybean Polysaccharide and Gelatin Interactions in Oil-Water Interface

Journal: Molecules

doi: 10.3390/molecules27092879

Elastic Modulus and Loss Modulus for samples at the oil–water interface. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).
Figure Legend Snippet: Elastic Modulus and Loss Modulus for samples at the oil–water interface. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).

Techniques Used:

Dynamic interfacial tension (γ) for sample solutions at the oil–water interface. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).
Figure Legend Snippet: Dynamic interfacial tension (γ) for sample solutions at the oil–water interface. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).

Techniques Used:

ITC titration curves of CP and hydrocolloids. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).
Figure Legend Snippet: ITC titration curves of CP and hydrocolloids. ( a ) CP-XG; ( b ) CP-SPSS; and ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).

Techniques Used: Titration

Intrinsic fluorescence intensity of CP-Hydrocolloid systems. ( a ) CP-XG; ( b ) CP-SPSS; ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).
Figure Legend Snippet: Intrinsic fluorescence intensity of CP-Hydrocolloid systems. ( a ) CP-XG; ( b ) CP-SPSS; ( c ) CP-Gelatin. (CP-Coconut protein, XG-Xanthan gum, SSPS-Soluble soybean polysaccharide).

Techniques Used: Fluorescence

5) Product Images from "Analysis of Environmental DNA and Edaphic Factors for the Detection of the Snail Intermediate Host Oncomelania hupensis quadrasi"

Article Title: Analysis of Environmental DNA and Edaphic Factors for the Detection of the Snail Intermediate Host Oncomelania hupensis quadrasi

Journal: Pathogens

doi: 10.3390/pathogens8040160

Positive correlation scatter plots of eDNA detection probability vs. ( A ) pH, ( B ) phosphorus, ( C ) potassium, ( D ) copper, ( E ) zinc calculated using Pearson Correlation in SPSS v. 16.
Figure Legend Snippet: Positive correlation scatter plots of eDNA detection probability vs. ( A ) pH, ( B ) phosphorus, ( C ) potassium, ( D ) copper, ( E ) zinc calculated using Pearson Correlation in SPSS v. 16.

Techniques Used:

6) Product Images from "Biological control of Erwinia mallotivora, the causal agent of papaya dieback disease by indigenous seed-borne endophytic lactic acid bacteria consortium"

Article Title: Biological control of Erwinia mallotivora, the causal agent of papaya dieback disease by indigenous seed-borne endophytic lactic acid bacteria consortium

Journal: PLoS ONE

doi: 10.1371/journal.pone.0224431

Dendrogram showing clustering and relationships of 24 potential isolates used in the study based on API 50 CH fermentation of 49 carbohydrates. The analysis was performed by calculating the Euclidean distance and the associations of isolates were constructed using the single linkage method (Nearest neighbour) in the IBM SPSS Statistic 22.0.
Figure Legend Snippet: Dendrogram showing clustering and relationships of 24 potential isolates used in the study based on API 50 CH fermentation of 49 carbohydrates. The analysis was performed by calculating the Euclidean distance and the associations of isolates were constructed using the single linkage method (Nearest neighbour) in the IBM SPSS Statistic 22.0.

Techniques Used: Construct

7) Product Images from "Investigation of cypermethrin toxicity in Swiss albino mice with physiological, genetic and biochemical approaches"

Article Title: Investigation of cypermethrin toxicity in Swiss albino mice with physiological, genetic and biochemical approaches

Journal: Scientific Reports

doi: 10.1038/s41598-022-15800-8

The effects of cypermethrin on MI. *Group I: control, Group II: 62.5 mg/kg b.w cypermethrin, Group III: 125 mg/kg b.w cypermethrin, Group IV: 250 mg/kg b.w cypermethrin. MI was calculated by analyzing 1000 cells per animal (for a total 6000 cells per group). Values are shown as mean ± SEM (n = 6). Data were analyzed with SPSS computer program using Duncan test and ANOVA variance analysis.
Figure Legend Snippet: The effects of cypermethrin on MI. *Group I: control, Group II: 62.5 mg/kg b.w cypermethrin, Group III: 125 mg/kg b.w cypermethrin, Group IV: 250 mg/kg b.w cypermethrin. MI was calculated by analyzing 1000 cells per animal (for a total 6000 cells per group). Values are shown as mean ± SEM (n = 6). Data were analyzed with SPSS computer program using Duncan test and ANOVA variance analysis.

Techniques Used:

8) Product Images from "Chemical changes of Angelicae Sinensis Radix and Chuanxiong Rhizoma by wine treatment: chemical profiling and marker selection by gas chromatography coupled with triple quadrupole mass spectrometry"

Article Title: Chemical changes of Angelicae Sinensis Radix and Chuanxiong Rhizoma by wine treatment: chemical profiling and marker selection by gas chromatography coupled with triple quadrupole mass spectrometry

Journal: Chinese Medicine

doi: 10.1186/1749-8546-8-12

Loading plots of PCA for ASR and CR. ( A, B ) Loading plots for crude and wine-treated ASR ( A ) and crude and wine-treated CR ( B ) using common components as the input data. The PCA was performed on the relative peak areas using SPSS for Windows 16.0 software.
Figure Legend Snippet: Loading plots of PCA for ASR and CR. ( A, B ) Loading plots for crude and wine-treated ASR ( A ) and crude and wine-treated CR ( B ) using common components as the input data. The PCA was performed on the relative peak areas using SPSS for Windows 16.0 software.

Techniques Used: Software

9) Product Images from "Resveratrol-induced brown fat-like phenotype in 3T3-L1 adipocytes partly via mTOR pathway"

Article Title: Resveratrol-induced brown fat-like phenotype in 3T3-L1 adipocytes partly via mTOR pathway

Journal: Food & Nutrition Research

doi: 10.29219/fnr.v64.3656

Effects of Res, rapamycin, and MHY1485 on expression of browning marker proteins via mammalian target of rapamycin (mTOR)-mediated pathway. Effects of rapamycin and MHY1485 on expression of mTOR (a) and browning marker proteins (d). The densitometric analysis of browning marker proteins (b and c) and ratio of phosphorylation to total mTOR (e and f). Rapamycin (10 nM) and MHY1485 (2 μM) were used to treat 3T3-L1 adipocytes for 6 days, and protein expression levels were determined by Western blotting. With or without treatment, each compound was indicated by ‘+’and ‘−’, respectively. All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post-hoc tests. Statistical significance between control and Res-treated groups is shown as * P
Figure Legend Snippet: Effects of Res, rapamycin, and MHY1485 on expression of browning marker proteins via mammalian target of rapamycin (mTOR)-mediated pathway. Effects of rapamycin and MHY1485 on expression of mTOR (a) and browning marker proteins (d). The densitometric analysis of browning marker proteins (b and c) and ratio of phosphorylation to total mTOR (e and f). Rapamycin (10 nM) and MHY1485 (2 μM) were used to treat 3T3-L1 adipocytes for 6 days, and protein expression levels were determined by Western blotting. With or without treatment, each compound was indicated by ‘+’and ‘−’, respectively. All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post-hoc tests. Statistical significance between control and Res-treated groups is shown as * P

Techniques Used: Expressing, Marker, Western Blot, Standard Deviation

Effects of resveratrol on lipid accumulation in 3T3-L1 adipocytes. Oil Red O staining of mature 3T3-L1 adipocytes captured at 200× magnifications (a) and relative optical density (OD) value determined at OD540 (b). Oil O Red images were from 3T3-L1 adipocytes treated with Res for 8 days. All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post hoc tests. Statistical significance between control and Res-treated groups is shown as * P
Figure Legend Snippet: Effects of resveratrol on lipid accumulation in 3T3-L1 adipocytes. Oil Red O staining of mature 3T3-L1 adipocytes captured at 200× magnifications (a) and relative optical density (OD) value determined at OD540 (b). Oil O Red images were from 3T3-L1 adipocytes treated with Res for 8 days. All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post hoc tests. Statistical significance between control and Res-treated groups is shown as * P

Techniques Used: Staining, Standard Deviation

Chemical structure of resveratrol (a). Effects of Res on expression of brown adipocytes-specific markers by Western blot analysis (b) and densitometric analysis of brown adipocytes markers (c). All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post-hoc tests. Statistical significance between control and Res-treated groups is shown as * P
Figure Legend Snippet: Chemical structure of resveratrol (a). Effects of Res on expression of brown adipocytes-specific markers by Western blot analysis (b) and densitometric analysis of brown adipocytes markers (c). All data are presented as the mean ± standard deviation (SD), and differences between groups were determined by one-way analysis of variance (ANOVA) using the Statistical Package of Social Science (SPSS, version 20.0; SPSS Inc.) program, followed by Tukey’s post-hoc tests. Statistical significance between control and Res-treated groups is shown as * P

Techniques Used: Expressing, Western Blot, Standard Deviation

10) Product Images from "Clinical evaluation of ocular biometry of dual Scheimpflug analyzer, GALILEI G6 and swept source optical coherence tomography, ANTERION"

Article Title: Clinical evaluation of ocular biometry of dual Scheimpflug analyzer, GALILEI G6 and swept source optical coherence tomography, ANTERION

Journal: Scientific Reports

doi: 10.1038/s41598-022-07696-1

Bland–Altman plot of the LT ( a ) and WTW ( b ) from GALILEI G6 and Anterion. The solid line represents the mean difference, whereas the dotted lines on each side show the upper and lower 95% LoA. Both LT and WTW plot demonstrate that only six eyes from the total of 96 were out of the 95% LoAs, indicating excellent concordance in LT and WTW calculation between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).
Figure Legend Snippet: Bland–Altman plot of the LT ( a ) and WTW ( b ) from GALILEI G6 and Anterion. The solid line represents the mean difference, whereas the dotted lines on each side show the upper and lower 95% LoA. Both LT and WTW plot demonstrate that only six eyes from the total of 96 were out of the 95% LoAs, indicating excellent concordance in LT and WTW calculation between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).

Techniques Used:

Bland–Altman plot of the IOL power using parameters from GALILEI G6 and ANTERION. The solid line represents the mean difference, whereas the dots on each side show the upper and lower 95% LoA. The plot demonstrates that six eyes at IOL power difference of ± 1.5 D (5 eyes) and 2 D (1 eye) from the total of 96 eyes were out of the 95% LoAs, indicating excellent agreement between the two devices’ measurement of IOL power. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).
Figure Legend Snippet: Bland–Altman plot of the IOL power using parameters from GALILEI G6 and ANTERION. The solid line represents the mean difference, whereas the dots on each side show the upper and lower 95% LoA. The plot demonstrates that six eyes at IOL power difference of ± 1.5 D (5 eyes) and 2 D (1 eye) from the total of 96 eyes were out of the 95% LoAs, indicating excellent agreement between the two devices’ measurement of IOL power. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).

Techniques Used:

Bland–Altman plot of the ACD ( a ) and AL ( b ) from GALILEI G6 and ANTERION. The solid line represents the mean difference, whereas the dotted lines on each side show the upper and lower 95% LoA. The ACD and AL plot demonstrate that only three and four eyes respectively of the total of 96 eyes were out of the 95% LoAs, indicating excellent agreement in ACD and AL between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).
Figure Legend Snippet: Bland–Altman plot of the ACD ( a ) and AL ( b ) from GALILEI G6 and ANTERION. The solid line represents the mean difference, whereas the dotted lines on each side show the upper and lower 95% LoA. The ACD and AL plot demonstrate that only three and four eyes respectively of the total of 96 eyes were out of the 95% LoAs, indicating excellent agreement in ACD and AL between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).

Techniques Used:

Bland–Altman plot of the prediction error using parameters from GALILEI G6 and ANTERION. The solid line represents the mean difference, while the dotted lines on each side show the upper and lower 95% LoA. The plot reveals that six eyes were out of the 95% LoAs. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).
Figure Legend Snippet: Bland–Altman plot of the prediction error using parameters from GALILEI G6 and ANTERION. The solid line represents the mean difference, while the dotted lines on each side show the upper and lower 95% LoA. The plot reveals that six eyes were out of the 95% LoAs. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).

Techniques Used:

Bland–Altman plot of K1 ( a ) and K2 ( b ) from GALILEI G6 and ANTERION. The solid line represents the mean difference, while the dotted lines on each side show the upper and lower 95% LoA. The K1 and K2 plot demonstrate that only four and five eyes respectively of the total 96 eyes were out of the 95% LoAs, indicating excellent K1 and K2 measurement agreement between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).
Figure Legend Snippet: Bland–Altman plot of K1 ( a ) and K2 ( b ) from GALILEI G6 and ANTERION. The solid line represents the mean difference, while the dotted lines on each side show the upper and lower 95% LoA. The K1 and K2 plot demonstrate that only four and five eyes respectively of the total 96 eyes were out of the 95% LoAs, indicating excellent K1 and K2 measurement agreement between the two devices. Created by SPSS (Version 22, SPSS Inc., IBM, Chicago, USA).

Techniques Used:

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    SPSS Inc spss 16 0 software
    Functional characterization of the three  TaNPSN s and  TaSYP132  using virus-induced gene silencing (VIGS) assay. (A) mild chlorotic mosaic symptoms were observed on newly expanded third leaves from plants inoculated with BSMV at 9 days post-inoculation (dpi) as a control. Photo-bleaching was evident on the newly expanded fourth leaves in plants pre-infected with BSMV-TaPDS at 14 dpi. (B) After inoculation of the newly expanded fourth leaves with  Pst  avirulent race CYR23. Note the increased number and size of necrotic spots on the wheat leaves pre-infected with BSMV-TaNPSN11, BSMV-TaNPSN13, and BSMV-TaSYP132 compared with those pre-infected with Mock, BSMV-00 and BSMV-TaNPSN12. (C) Relative transcript levels of the three  TaNPSN s and  TaSYP132  in corresponding knockdown plants assayed by qRT-PCR. Leaf samples were collected from plants pre-infected with BSMV-00, BSMV-TaNPSN11, BSMV-TaNPSN12, BSMV-TaNPSN13, and BSMV-TaSYP132 at 24, 48 and 120 hours post-inoculation (hpi) with  Pst  avirulent race CYR23. The relative expression of  TaNPSN s and  TaSYP132  was calculated using the comparative threshold (2 –ΔΔCT ) method. The mean, standard deviation and two-sample  t -tests were calculated by SPSS 16.0 software with data from three independent biological replicates. Mock, wheat leaves treated with 1 × Fes buffer; BSMV, Barley Stripe Mosaic Virus. (This figure is available in colour at  JXB  online.)
    Spss 16 0 Software, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 99/100, based on 473 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Behavioral results for the hole-board test. Young males (YM) performed better than old impaired males (OMI) showing higher reference memory indices (RMI) but not compared to old unimpaired males (OMI) whereas between YM and OMU there was no difference (for statistics see the section “Results”). Given are the mean values and standard errors of the mean, n = 10 for each group). Statistics: 10 animals per group; data analyzed by <t>SPSS</t> Version 22 software (IBM ® SPSS ® Statistics) using general linear model – repeated measures ANOVA; the significance cut-off was set at p
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    SPSS Inc ibm spss software
    Differences of cytokine expression in mPBMCs and PBMCs in children with cerebral palsy. The expression of IL-6 was significantly increased in mPBMCs ( n = 14) than in PBMCs ( n = 14, P = 0.035), and IL-3 was significantly decreased in mPBMCs as compared to PBMCs ( P = 0.048). The Wilcoxon signed-rank test, Kriskal-Wallis tests and Mann Whitney U test were used for inter-group comparisons. All statistical analyses were conducted using <t>IBM</t> <t>SPSS</t> software. The data were expressed as the mean ± SD and * P
    Ibm Spss Software, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Functional characterization of the three  TaNPSN s and  TaSYP132  using virus-induced gene silencing (VIGS) assay. (A) mild chlorotic mosaic symptoms were observed on newly expanded third leaves from plants inoculated with BSMV at 9 days post-inoculation (dpi) as a control. Photo-bleaching was evident on the newly expanded fourth leaves in plants pre-infected with BSMV-TaPDS at 14 dpi. (B) After inoculation of the newly expanded fourth leaves with  Pst  avirulent race CYR23. Note the increased number and size of necrotic spots on the wheat leaves pre-infected with BSMV-TaNPSN11, BSMV-TaNPSN13, and BSMV-TaSYP132 compared with those pre-infected with Mock, BSMV-00 and BSMV-TaNPSN12. (C) Relative transcript levels of the three  TaNPSN s and  TaSYP132  in corresponding knockdown plants assayed by qRT-PCR. Leaf samples were collected from plants pre-infected with BSMV-00, BSMV-TaNPSN11, BSMV-TaNPSN12, BSMV-TaNPSN13, and BSMV-TaSYP132 at 24, 48 and 120 hours post-inoculation (hpi) with  Pst  avirulent race CYR23. The relative expression of  TaNPSN s and  TaSYP132  was calculated using the comparative threshold (2 –ΔΔCT ) method. The mean, standard deviation and two-sample  t -tests were calculated by SPSS 16.0 software with data from three independent biological replicates. Mock, wheat leaves treated with 1 × Fes buffer; BSMV, Barley Stripe Mosaic Virus. (This figure is available in colour at  JXB  online.)

    Journal: Journal of Experimental Botany

    Article Title: Wheat TaNPSN SNARE homologues are involved in vesicle-mediated resistance to stripe rust (Puccinia striiformis f. sp. tritici)

    doi: 10.1093/jxb/eru241

    Figure Lengend Snippet: Functional characterization of the three TaNPSN s and TaSYP132 using virus-induced gene silencing (VIGS) assay. (A) mild chlorotic mosaic symptoms were observed on newly expanded third leaves from plants inoculated with BSMV at 9 days post-inoculation (dpi) as a control. Photo-bleaching was evident on the newly expanded fourth leaves in plants pre-infected with BSMV-TaPDS at 14 dpi. (B) After inoculation of the newly expanded fourth leaves with Pst avirulent race CYR23. Note the increased number and size of necrotic spots on the wheat leaves pre-infected with BSMV-TaNPSN11, BSMV-TaNPSN13, and BSMV-TaSYP132 compared with those pre-infected with Mock, BSMV-00 and BSMV-TaNPSN12. (C) Relative transcript levels of the three TaNPSN s and TaSYP132 in corresponding knockdown plants assayed by qRT-PCR. Leaf samples were collected from plants pre-infected with BSMV-00, BSMV-TaNPSN11, BSMV-TaNPSN12, BSMV-TaNPSN13, and BSMV-TaSYP132 at 24, 48 and 120 hours post-inoculation (hpi) with Pst avirulent race CYR23. The relative expression of TaNPSN s and TaSYP132 was calculated using the comparative threshold (2 –ΔΔCT ) method. The mean, standard deviation and two-sample t -tests were calculated by SPSS 16.0 software with data from three independent biological replicates. Mock, wheat leaves treated with 1 × Fes buffer; BSMV, Barley Stripe Mosaic Virus. (This figure is available in colour at JXB online.)

    Article Snippet: Calculations for the mean, standard error and two-sample t -tests for the statistics were performed using SPSS 16.0 software (SPSS Inc.).

    Techniques: Functional Assay, VIGS Assay, Infection, Quantitative RT-PCR, Expressing, Standard Deviation, Software

    The relative expressions of the three  TaNPSN s and  TaSYP132  in wheat leaves challenged by  Pst  infection using qRT-PCR assay. Leaf samples were collected at 0, 12, 18, 24, 48, 72 and 120 hours post-inoculation (hpi) with  Pst  avirulent race (CYR23) and virulent race (CYR32), respectively. The Y scale indicates transcript levels relative to endogenous control  EF1a . The mean, standard error and two-sample  t -tests were calculated by SPSS 16.0 software with data from three independent biological replicates. (This figure is available in colour at  JXB  online.)

    Journal: Journal of Experimental Botany

    Article Title: Wheat TaNPSN SNARE homologues are involved in vesicle-mediated resistance to stripe rust (Puccinia striiformis f. sp. tritici)

    doi: 10.1093/jxb/eru241

    Figure Lengend Snippet: The relative expressions of the three TaNPSN s and TaSYP132 in wheat leaves challenged by Pst infection using qRT-PCR assay. Leaf samples were collected at 0, 12, 18, 24, 48, 72 and 120 hours post-inoculation (hpi) with Pst avirulent race (CYR23) and virulent race (CYR32), respectively. The Y scale indicates transcript levels relative to endogenous control EF1a . The mean, standard error and two-sample t -tests were calculated by SPSS 16.0 software with data from three independent biological replicates. (This figure is available in colour at JXB online.)

    Article Snippet: Calculations for the mean, standard error and two-sample t -tests for the statistics were performed using SPSS 16.0 software (SPSS Inc.).

    Techniques: Infection, Quantitative RT-PCR, Software

    Effect of 0.04 ppm paraquat on lipid peroxidation at various developmental stages of zebrafish following exposure during the window of dopamine neurogenesis i.e., at 18 hpf. Statistical significance determined by a Multivariate analysis (the developmental stage and treatment as covariates; the MDA levels as dependent variable, respectively) was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of the MDA levels at various developmental stages in paraquat exposed and control. (* = p

    Journal: Toxicology Reports

    Article Title: Paraquat exposure induces behavioral deficits in larval zebrafish during the window of dopamine neurogenesis

    doi: 10.1016/j.toxrep.2015.06.007

    Figure Lengend Snippet: Effect of 0.04 ppm paraquat on lipid peroxidation at various developmental stages of zebrafish following exposure during the window of dopamine neurogenesis i.e., at 18 hpf. Statistical significance determined by a Multivariate analysis (the developmental stage and treatment as covariates; the MDA levels as dependent variable, respectively) was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of the MDA levels at various developmental stages in paraquat exposed and control. (* = p

    Article Snippet: A multivariate analysis (the developmental stage and treatment as covariates; the lipid peroxidation and GSH levels as dependent variable, respectively) was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of viability, GSH level and Lipid peroxidation at various developmental stages in parquat exposed and control. (* = p < 0.0001,** = p < 0.002).

    Techniques: Multiple Displacement Amplification, Software

    Effect of 0.04 ppm paraquat on GSH levels at various developmental stages of zebrafish following exposure during the window of dopamine neurogenesis i.e., at 18 hpf Statistical significance was determined by Multivariate analysis (the developmental stage and treatment as covariates; the GSH levels as dependent variable, respectively) which was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of the GSH levels at various developmental stages in paraquat exposed and control embryos. (* = p

    Journal: Toxicology Reports

    Article Title: Paraquat exposure induces behavioral deficits in larval zebrafish during the window of dopamine neurogenesis

    doi: 10.1016/j.toxrep.2015.06.007

    Figure Lengend Snippet: Effect of 0.04 ppm paraquat on GSH levels at various developmental stages of zebrafish following exposure during the window of dopamine neurogenesis i.e., at 18 hpf Statistical significance was determined by Multivariate analysis (the developmental stage and treatment as covariates; the GSH levels as dependent variable, respectively) which was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of the GSH levels at various developmental stages in paraquat exposed and control embryos. (* = p

    Article Snippet: A multivariate analysis (the developmental stage and treatment as covariates; the lipid peroxidation and GSH levels as dependent variable, respectively) was performed using the SPSS software version 16.0 to evaluate the differences in the mean value of viability, GSH level and Lipid peroxidation at various developmental stages in parquat exposed and control. (* = p < 0.0001,** = p < 0.002).

    Techniques: Software

    Behavioral results for the hole-board test. Young males (YM) performed better than old impaired males (OMI) showing higher reference memory indices (RMI) but not compared to old unimpaired males (OMI) whereas between YM and OMU there was no difference (for statistics see the section “Results”). Given are the mean values and standard errors of the mean, n = 10 for each group). Statistics: 10 animals per group; data analyzed by SPSS Version 22 software (IBM ® SPSS ® Statistics) using general linear model – repeated measures ANOVA; the significance cut-off was set at p

    Journal: Frontiers in Aging Neuroscience

    Article Title: Differences in Hypothalamic Lipid Profiles of Young and Aged Male Rats With Impaired and Unimpaired Spatial Cognitive Abilities and Memory

    doi: 10.3389/fnagi.2020.00204

    Figure Lengend Snippet: Behavioral results for the hole-board test. Young males (YM) performed better than old impaired males (OMI) showing higher reference memory indices (RMI) but not compared to old unimpaired males (OMI) whereas between YM and OMU there was no difference (for statistics see the section “Results”). Given are the mean values and standard errors of the mean, n = 10 for each group). Statistics: 10 animals per group; data analyzed by SPSS Version 22 software (IBM ® SPSS ® Statistics) using general linear model – repeated measures ANOVA; the significance cut-off was set at p

    Article Snippet: To determine statistical significance of the differences over the entire training between all groups of rats, the data were analyzed by SPSS Version 22 software (IBM® SPSS® Statistics) using general linear model – repeated measures ANOVA.

    Techniques: Software

    Differences of cytokine expression in mPBMCs and PBMCs in children with cerebral palsy. The expression of IL-6 was significantly increased in mPBMCs ( n = 14) than in PBMCs ( n = 14, P = 0.035), and IL-3 was significantly decreased in mPBMCs as compared to PBMCs ( P = 0.048). The Wilcoxon signed-rank test, Kriskal-Wallis tests and Mann Whitney U test were used for inter-group comparisons. All statistical analyses were conducted using IBM SPSS software. The data were expressed as the mean ± SD and * P

    Journal: Neural Regeneration Research

    Article Title: Mononuclear cells from the cord blood and granulocytecolony stimulating factor-mobilized peripheral blood: is there a potential for treatment of cerebral palsy?

    doi: 10.4103/1673-5374.172321

    Figure Lengend Snippet: Differences of cytokine expression in mPBMCs and PBMCs in children with cerebral palsy. The expression of IL-6 was significantly increased in mPBMCs ( n = 14) than in PBMCs ( n = 14, P = 0.035), and IL-3 was significantly decreased in mPBMCs as compared to PBMCs ( P = 0.048). The Wilcoxon signed-rank test, Kriskal-Wallis tests and Mann Whitney U test were used for inter-group comparisons. All statistical analyses were conducted using IBM SPSS software. The data were expressed as the mean ± SD and * P

    Article Snippet: All statistical analyses were conducted using IBM SPSS software (version 21; IBM Co., Armonk, NY, USA).

    Techniques: Expressing, MANN-WHITNEY, Software

    Differences in cytokine expression in mPBMCs and PBMCs from healthy adults. The expression of IL-1β ( P = 0.048) and IL-6 ( P = 0.006) was significantly increased in mPBMCs ( n = 14) than in PBMCs ( n = 14). The Wilcoxon signed-rank test, Kriskal-Wallis test and Mann Whitney U test were used for intergroup comparisons. All statistical analyses were conducted using IBM SPSS software. The data were expressed as the mean ± SD and * P

    Journal: Neural Regeneration Research

    Article Title: Mononuclear cells from the cord blood and granulocytecolony stimulating factor-mobilized peripheral blood: is there a potential for treatment of cerebral palsy?

    doi: 10.4103/1673-5374.172321

    Figure Lengend Snippet: Differences in cytokine expression in mPBMCs and PBMCs from healthy adults. The expression of IL-1β ( P = 0.048) and IL-6 ( P = 0.006) was significantly increased in mPBMCs ( n = 14) than in PBMCs ( n = 14). The Wilcoxon signed-rank test, Kriskal-Wallis test and Mann Whitney U test were used for intergroup comparisons. All statistical analyses were conducted using IBM SPSS software. The data were expressed as the mean ± SD and * P

    Article Snippet: All statistical analyses were conducted using IBM SPSS software (version 21; IBM Co., Armonk, NY, USA).

    Techniques: Expressing, MANN-WHITNEY, Software