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e. coli gene expression microarray microarray 8×15 k  (Agilent technologies)


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    Structured Review

    Agilent technologies e. coli gene expression microarray microarray 8×15 k
    EvgAS > YdeO > DctR/NhaR/GadE/GadW regulatory network in <t>E.</t> <t>coli</t> .
    E. Coli Gene Expression Microarray Microarray 8×15 K, 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
    https://www.bioz.com/product/e%2E+coli+gene+expression+microarrays/pmc04222967-154-1-9
    Average 90 stars, based on 1 article reviews
    e. coli gene expression microarray microarray 8×15 k - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Characterization of the YdeO Regulon in Escherichia coli"

    Article Title: Characterization of the YdeO Regulon in Escherichia coli

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0111962

    EvgAS > YdeO > DctR/NhaR/GadE/GadW regulatory network in E. coli .
    Figure Legend Snippet: EvgAS > YdeO > DctR/NhaR/GadE/GadW regulatory network in E. coli .

    Techniques Used:

    Related Articles

    Labeling:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Expressing:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Microarray:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Mutagenesis:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Incubation:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Transformation Assay:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.

    Isolation:

    Article Title: Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in E scherichia coli
    Article Snippet: Six hundred nanograms of labelled cDNA was hybridized overnight to Agilent E. coli Gene Expression Microarrays then immediately washed and scanned using an Aglient SureScan microarray scanner in accordance with the recommended procedure.

    Article Title: Engineering of a Synthetic Metabolic Pathway for the Assimilation of (d)-Xylose into Value-Added Chemicals.
    Article Snippet: 2 2 A synthetic pathway for (D)-xylose assimilation was stoichiometrically evaluated and 3 implemented in Escherichia coli strains.. The pathway proceeds via isomerization of (D)-xylose to (D)-4 xylulose, phosphorylation of (D)-xylulose to obtain (D)-xylulose-1-phosphate (X1P), and aldolytic 5 cleavage of the latter to yield glycolaldehyde and DHAP.. Stoichiometric analyses showed that this 6 pathway provides access to ethylene glycol with a theoretical molar yield of 1.

    Article Title: Optimization of ethylene glycol production from ( d )-xylose via a synthetic pathway implemented in Escherichia coli
    Article Snippet: The Low Input Quick Amp Labeling kit (Agilent) was used to convert RNA samples to labeled cDNA which was hybridized on E. coli Gene Expression Microarrays (8 × 15 K, Agilent) following the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol.



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    Image Search Results


    EvgAS > YdeO > DctR/NhaR/GadE/GadW regulatory network in E. coli .

    Journal: PLoS ONE

    Article Title: Characterization of the YdeO Regulon in Escherichia coli

    doi: 10.1371/journal.pone.0111962

    Figure Lengend Snippet: EvgAS > YdeO > DctR/NhaR/GadE/GadW regulatory network in E. coli .

    Article Snippet: The E. coli Gene Expression Microarray microarray 8×15 K (Agilent) was used.

    Techniques: