kinetic model identification tools Search Results


spectramax id5 multi mode microplate reader  (Danaher Inc)
97
Danaher Inc spectramax id5 multi mode microplate reader
Spectramax Id5 Multi Mode Microplate Reader, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinetic+model+identification+tools/SpectraMax+iD5+Multi-Mode+Microplate+Reader+with+injectors/pm34514924-81-28-33
Average 97 stars, based on 1 article reviews
spectramax id5 multi mode microplate reader - by Bioz Stars, 2026-10
97/100 stars
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microplate reader  (Danaher Inc)
99
Danaher Inc microplate reader
Microplate Reader, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinetic+model+identification+tools/SpectraMax+ABS+PLUS+Microplate+Reader/pm35634373-50-20-22
Average 99 stars, based on 1 article reviews
microplate reader - by Bioz Stars, 2026-10
99/100 stars
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kinetics neo software package  (NETZSCH)
90
NETZSCH kinetics neo software package
Kinetics Neo Software Package, supplied by NETZSCH, 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/product/kinetic+model+identification+tools/kinetics+neo+software/10__1002_slash_pat__5060-46-14-20
Average 90 stars, based on 1 article reviews
kinetics neo software package - by Bioz Stars, 2026-10
90/100 stars
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software pmod version 2.85  (PMOD Technologies)
90
PMOD Technologies software pmod version 2.85
Software Pmod Version 2.85, supplied by PMOD Technologies, 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/product/kinetic+model+identification+tools/pmod+software+package/pm18797470-113-8-11
Average 90 stars, based on 1 article reviews
software pmod version 2.85 - by Bioz Stars, 2026-10
90/100 stars
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s. cerevisiae kinetic glycolysis model  (Biomodels LLC)
90
Biomodels LLC s. cerevisiae kinetic glycolysis model
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
S. Cerevisiae Kinetic Glycolysis Model, supplied by Biomodels LLC, 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/product/kinetic+model+identification+tools/dynamic+model+of+the+central+carbon+metabolism+of+e++coli/pmc06167078-20-0-7
Average 90 stars, based on 1 article reviews
s. cerevisiae kinetic glycolysis model - by Bioz Stars, 2026-10
90/100 stars
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chi-square test  (CH Instruments)
90
CH Instruments chi-square test
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
Chi Square Test, supplied by CH Instruments, 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/product/kinetic+model+identification+tools/chi+square+test/pmc10070660-94-13-13
Average 90 stars, based on 1 article reviews
chi-square test - by Bioz Stars, 2026-10
90/100 stars
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r928 photomultiplier tube  (Hamamatsu)
90
Hamamatsu r928 photomultiplier tube
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
R928 Photomultiplier Tube, supplied by Hamamatsu, 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/product/kinetic+model+identification+tools/photomultiplier+tube+hamamatsu+r928/pm39352411__ja4c08927_si_001-151-21-21
Average 90 stars, based on 1 article reviews
r928 photomultiplier tube - by Bioz Stars, 2026-10
90/100 stars
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software supported modelling in pharmacokinetics  (Verlag GmbH)
90
Verlag GmbH software supported modelling in pharmacokinetics
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
Software Supported Modelling In Pharmacokinetics, supplied by Verlag GmbH, 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/product/kinetic+model+identification+tools/software+supported+modelling+in+pharmacokinetics/10__1007_slash_11875741-3466-11-3
Average 90 stars, based on 1 article reviews
software supported modelling in pharmacokinetics - by Bioz Stars, 2026-10
90/100 stars
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nanomedicine  (NanoCarrier Co)
90
NanoCarrier Co nanomedicine
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
Nanomedicine, supplied by NanoCarrier Co, 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/product/kinetic+model+identification+tools/nanomedicines/10__1016_slash_j__onano__2023__100167-13-133-119
Average 90 stars, based on 1 article reviews
nanomedicine - by Bioz Stars, 2026-10
90/100 stars
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96-well plates  (Corning Life Sciences)
90
Corning Life Sciences 96-well plates
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
96 Well Plates, supplied by Corning Life Sciences, 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/product/kinetic+model+identification+tools/96+well+plates/pmc05939596-404-21-23
Average 90 stars, based on 1 article reviews
96-well plates - by Bioz Stars, 2026-10
90/100 stars
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real time pcr  (Bio-Rad)
99
Bio-Rad real time pcr
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
Real Time Pcr, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinetic+model+identification+tools/CFX96+and+CFX384+Real-Time+PCR+Detection+Systems+Firmware+Update/us12357601-165-19-23
Average 99 stars, based on 1 article reviews
real time pcr - by Bioz Stars, 2026-10
99/100 stars
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langmuir kinetics model  (Nicoya Lifesciences)
86
Nicoya Lifesciences langmuir kinetics model
The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. <t>cerevisiae</t> . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .
Langmuir Kinetics Model, supplied by Nicoya Lifesciences, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinetic+model+identification+tools/langmuir+model/pmc12582022-112-45-52
Average 86 stars, based on 1 article reviews
langmuir kinetics model - by Bioz Stars, 2026-10
86/100 stars
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Image Search Results


The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. cerevisiae . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .

Journal: Cell Systems

Article Title: Machine Learning Predicts the Yeast Metabolome from the Quantitative Proteome of Kinase Knockouts

doi: 10.1016/j.cels.2018.08.001

Figure Lengend Snippet: The Deletion of Each Yeast Kinase Triggers a Unique Reconfiguration of Enzyme Expression in the Cell (A) Similarity and overlap between enzyme expression proteomes obtained upon kinase deletion in S. cerevisiae . Each cell represents the overlap in the compendium of differentially expressed enzymes (relative to the parental strain BY4741-pHLUM) between any pair of kinase knockouts. An enzyme is considered differentially expressed if the fold change > |log 2 (1.4/0.714)|, BH adj. p < 0.01. The matrix distinguishes between upregulated (red, upper right part of the matrix) and downregulated (blue, lower left part) enzymes. For illustration purposes, rows and columns are clustered according to the Jaccard distance between the proteomes, disregarding the directionality of the expression changes. The overlap between each pair of proteomes is shown as Jaccard similarity. (B) The fraction of differentially expressed metabolic enzymes in comparison to total differential protein expression in all kinase mutants (bar chart). The absolute average similarity of kinase deletion enzyme proteomes, across all kinase mutants, is depicted as a black line. The typical kinase deletion causes a unique enzyme expression signature, with a median dissimilarity between kinase proteome pairs of 88% (average overlap between enzymes differentially expressed = 12%). (C) The typical overlap of perturbed enzyme proteomes in kinases mutants is not more than ∼25% (dotted median line). (D) Enzyme expression changes (log 2 -fold change) are not better explained by the signaling pathway annotations as obtained from KEGG or Reactome databases compared to randomly assembled pathways. More comparisons are provided in and .

Article Snippet: S. cerevisiae kinetic glycolysis model , , BioModels: MODEL1303260018.

Techniques: Expressing, Comparison

Journal: Cell Systems

Article Title: Machine Learning Predicts the Yeast Metabolome from the Quantitative Proteome of Kinase Knockouts

doi: 10.1016/j.cels.2018.08.001

Figure Lengend Snippet:

Article Snippet: S. cerevisiae kinetic glycolysis model , , BioModels: MODEL1303260018.

Techniques: Recombinant, Plasmid Preparation, Software, Control