database file maker pro 7.0 software Search Results


database file maker pro 7.0 software  (FileMaker Inc)
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FileMaker Inc database file maker pro 7.0 software
Database File Maker Pro 7.0 Software, supplied by FileMaker Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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17 software 27  (STATA Corporation)
99
STATA Corporation 17 software 27
17 Software 27, supplied by STATA Corporation, 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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proteome discoverer software  (Thermo Fisher)
86
Thermo Fisher proteome discoverer software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Proteome Discoverer Software, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteome discoverer software - by Bioz Stars, 2026-03
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xcalibur software  (Thermo Fisher)
90
Thermo Fisher xcalibur software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Xcalibur Software, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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xcalibur software - by Bioz Stars, 2026-03
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peaks software (version 4.2  (Bioinformatics Solutions Inc)
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Bioinformatics Solutions Inc peaks software (version 4.2
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Peaks Software (Version 4.2, supplied by Bioinformatics Solutions Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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peaks software (version 4.2 - by Bioz Stars, 2026-03
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li cor file viewer software  (LI-COR)
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LI-COR li cor file viewer software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Li Cor File Viewer Software, supplied by LI-COR, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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stata statistical software  (STATA Corporation)
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STATA Corporation stata statistical software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Stata Statistical Software, supplied by STATA Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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stata statistical software - by Bioz Stars, 2026-03
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matlab r2015a software  (MathWorks Inc)
90
MathWorks Inc matlab r2015a software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Matlab R2015a Software, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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relational database file maker pro 13  (FileMaker Inc)
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FileMaker Inc relational database file maker pro 13
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Relational Database File Maker Pro 13, supplied by FileMaker Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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relational database file maker pro 13 - by Bioz Stars, 2026-03
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stata 17.0 software  (STATA Corporation)
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STATA Corporation stata 17.0 software
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Stata 17.0 Software, supplied by STATA Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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database swissprot  (Proteome Software Inc)
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Proteome Software Inc database swissprot
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Database Swissprot, supplied by Proteome Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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software package 'file-maker pro  (FileMaker Inc)
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FileMaker Inc software package 'file-maker pro
Validation of the <t>proteome</t> data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image <t>J</t> <t>software</t> and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.
Software Package 'file Maker Pro, supplied by FileMaker Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Validation of the proteome data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image J software and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.

Journal: Molecular & Cellular Proteomics : MCP

Article Title: Integrated Transcriptomic and Proteomic Analysis of the Global Response of Synechococcus to High Light Stress *

doi: 10.1074/mcp.M114.046003

Figure Lengend Snippet: Validation of the proteome data and transcriptome data. A, Comparison of log2 expression of 20 selected differentially regulated genes measured by RNA-Seq and qRT-PCR. Positive and negative log2 expression ratios represent up- and down-regulation after HL exposure, respectively. Each data point is calculated from averages of biological triplicates. B, Results derived from RNA-Seq analysis (white bars; n = 2) were compared with those from qRT-PCR (gray bars; n = 3). C, Western blot analysis of protein expression levels of five representative proteins quantified by proteomics after HL exposure. Fold changes of protein levels were determined using Image J software and normalized by protein concentration. D, The mRNA expression level of the validated proteins as detected by qRT-PCR.

Article Snippet: Database Search Raw data files were processed to generate peak list files using Proteome Discoverer software (Thermo Fisher Scientific, v. 1.3.0.339).

Techniques: Expressing, RNA Sequencing Assay, Quantitative RT-PCR, Derivative Assay, Western Blot, Software, Protein Concentration