data analysis software chart v. 5.0.1 Search Results


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LI-COR li cor odyssey clx
Li Cor Odyssey Clx, supplied by LI-COR, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GraphPad Software Inc ms excel and graphpad prism 5.01 software
Ms Excel And Graphpad Prism 5.01 Software, supplied by GraphPad 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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GraphPad Software Inc prism 5 software
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GraphPad Software Inc prism 5.01 software
Prism 5.01 Software, supplied by GraphPad 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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RStudio software r studio
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SAS institute software package jmp 5.0.1a
Software Package Jmp 5.0.1a, supplied by SAS institute, 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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SAS institute statview software
Statview Software, supplied by SAS institute, 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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Inforsense Ltd inforsense 5.0.1
Inforsense 5.0.1, supplied by Inforsense Ltd, 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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Agilent technologies masshunter lc-ms data acquisition software (version b.05.01, build 5.01.5125.2
ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. <t>LC-MS</t> traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text
Masshunter Lc Ms Data Acquisition Software (Version B.05.01, Build 5.01.5125.2, supplied by Agilent technologies, 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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SAS institute jmp software 5.0.1j
ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. <t>LC-MS</t> traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text
Jmp Software 5.0.1j, supplied by SAS institute, 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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Abacus Concepts statview statistical package version 5.0.1
ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. <t>LC-MS</t> traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text
Statview Statistical Package Version 5.0.1, supplied by Abacus Concepts, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/statview statistical package version 5.0.1/product/Abacus Concepts
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statview statistical package version 5.0.1 - by Bioz Stars, 2026-04
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Adept Scientific Inc analysis of variance (anova) statview 5.0.1
ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. <t>LC-MS</t> traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text
Analysis Of Variance (Anova) Statview 5.0.1, supplied by Adept Scientific 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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analysis of variance (anova) statview 5.0.1 - by Bioz Stars, 2026-04
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ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. LC-MS traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text

Journal: BMC Genomics

Article Title: A comprehensive multi-omics approach uncovers adaptations for growth and survival of Pseudomonas aeruginosa on n -alkanes

doi: 10.1186/s12864-017-3708-4

Figure Lengend Snippet: ATCC 33988 does not use rhamnolipids to improve n -alkane degradation. ( a ) Rhamnolipid synthesis pathway: RhlI produces the autoinducer N-butyryl-DL-homoserine lactone (C 4 -HSL.) When levels of C 4 -HSL reach a threshold limit, they activate the transcription factor RhlR. RhlR increases transcription of the rhamnolipid biosynthetic enzymes RhlA, RhlB and RhlC, which produce rhamnolipids. ( b ) Heat map representing the fold-change in total RNA (column R), ribosome footprints (column F) and protein (column P) of genes in the rhamnolipid synthesis pathway. All expression values are log 2 -transformed. Undetected genes are shaded grey. If a gene is not present in ATCC 33988, the log 2 (fold-change) is given the value 1. LC-MS traces of the autoinducer molecule C 4 -HSL ( c ) and a sample di-rhamnolipid ( d ) in the extracellular media. e Surface tension of each culture. * indicates p < 0.05 for data discussed in the text

Article Snippet: Data acquisition was performed using Agilent MassHunter LC-MS Data Acquisition Software (version B.05.01, build 5.01.5125.2).

Techniques: Expressing, Transformation Assay, Liquid Chromatography with Mass Spectroscopy

ATCC 33988 shows muted expression from the QS network. ( a ) Schematic showing QS autoinducer synthesis genes and cognate receptors for in Pseudomonas aeruginosa as discussed in text. LC-MS traces of the autoinducer molecules ( b ) 3-oxo-C 12 -HSL and ( c ) PQS in the extracellular media. Triangles represent putative PQS isomers with different retention times but the same exact mass as the PQS standard

Journal: BMC Genomics

Article Title: A comprehensive multi-omics approach uncovers adaptations for growth and survival of Pseudomonas aeruginosa on n -alkanes

doi: 10.1186/s12864-017-3708-4

Figure Lengend Snippet: ATCC 33988 shows muted expression from the QS network. ( a ) Schematic showing QS autoinducer synthesis genes and cognate receptors for in Pseudomonas aeruginosa as discussed in text. LC-MS traces of the autoinducer molecules ( b ) 3-oxo-C 12 -HSL and ( c ) PQS in the extracellular media. Triangles represent putative PQS isomers with different retention times but the same exact mass as the PQS standard

Article Snippet: Data acquisition was performed using Agilent MassHunter LC-MS Data Acquisition Software (version B.05.01, build 5.01.5125.2).

Techniques: Expressing, Liquid Chromatography with Mass Spectroscopy