array designer 1.1 Search Results


11 k microarray platform  (Agilent technologies)
90
Agilent technologies 11 k microarray platform
11 K Microarray Platform, 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/result/11 k microarray platform/product/Agilent technologies
Average 90 stars, based on 1 article reviews
11 k microarray platform - by Bioz Stars, 2026-04
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oligo array  (Agilent technologies)
90
Agilent technologies oligo array
Oligo Array, 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/result/oligo array/product/Agilent technologies
Average 90 stars, based on 1 article reviews
oligo array - by Bioz Stars, 2026-04
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visium  (10X Genomics)
90
10X Genomics visium
Visium, supplied by 10X Genomics, 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/visium/product/10X Genomics
Average 90 stars, based on 1 article reviews
visium - by Bioz Stars, 2026-04
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multi-camera array blackmagic micro cinema camera  (Blackmagic Design Pty Ltd)
90
Blackmagic Design Pty Ltd multi-camera array blackmagic micro cinema camera
Multi Camera Array Blackmagic Micro Cinema Camera, supplied by Blackmagic Design Pty 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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Average 90 stars, based on 1 article reviews
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microarray probe sequences  (Agilent technologies)
90
Agilent technologies microarray probe sequences
Microarray Probe Sequences, 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/result/microarray probe sequences/product/Agilent technologies
Average 90 stars, based on 1 article reviews
microarray probe sequences - by Bioz Stars, 2026-04
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e. coli mg1655 8 × 15k array (gt_cat_11; amadid number 019439)  (Agilent technologies)
90
Agilent technologies e. coli mg1655 8 × 15k array (gt_cat_11; amadid number 019439)
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
E. Coli Mg1655 8 × 15k Array (Gt Cat 11; Amadid Number 019439), 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/result/e. coli mg1655 8 × 15k array (gt_cat_11; amadid number 019439)/product/Agilent technologies
Average 90 stars, based on 1 article reviews
e. coli mg1655 8 × 15k array (gt_cat_11; amadid number 019439) - by Bioz Stars, 2026-04
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alt r crispr cas9 crrna  (Danaher Inc)
95
Danaher Inc alt r crispr cas9 crrna
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
Alt R Crispr Cas9 Crrna, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/alt r crispr cas9 crrna/product/Danaher Inc
Average 95 stars, based on 1 article reviews
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agilent’s custom-designed whole-genome array  (Baylor Genetics)
90
Baylor Genetics agilent’s custom-designed whole-genome array
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
Agilent’s Custom Designed Whole Genome Array, supplied by Baylor Genetics, 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/agilent’s custom-designed whole-genome array/product/Baylor Genetics
Average 90 stars, based on 1 article reviews
agilent’s custom-designed whole-genome array - by Bioz Stars, 2026-04
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meningococcal resequencing microarray (mrm  (Thermo Fisher)
90
Thermo Fisher meningococcal resequencing microarray (mrm
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
Meningococcal Resequencing Microarray (Mrm, 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
https://www.bioz.com/result/meningococcal resequencing microarray (mrm/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
meningococcal resequencing microarray (mrm - by Bioz Stars, 2026-04
90/100 stars
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244,000 feature gene expression microarrays  (Agilent technologies)
90
Agilent technologies 244,000 feature gene expression microarrays
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
244,000 Feature Gene Expression Microarrays, 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/result/244,000 feature gene expression microarrays/product/Agilent technologies
Average 90 stars, based on 1 article reviews
244,000 feature gene expression microarrays - by Bioz Stars, 2026-04
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microarray immunochip  (Illumina Inc)
90
Illumina Inc microarray immunochip
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
Microarray Immunochip, supplied by Illumina Inc, 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/microarray immunochip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
microarray immunochip - by Bioz Stars, 2026-04
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zno nanorod array structures  (Kuang Lung Shing)
90
Kuang Lung Shing zno nanorod array structures
PNP supported growth of E. coli <t>MG1655</t> (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.
Zno Nanorod Array Structures, supplied by Kuang Lung Shing, 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/zno nanorod array structures/product/Kuang Lung Shing
Average 90 stars, based on 1 article reviews
zno nanorod array structures - by Bioz Stars, 2026-04
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Image Search Results


PNP supported growth of E. coli MG1655 (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.

Journal: The Journal of Biological Chemistry

Article Title: The Organophosphate Degradation ( opd ) Island-borne Esterase-induced Metabolic Diversion in Escherichia coli and Its Influence on p -Nitrophenol Degradation *

doi: 10.1074/jbc.M115.661249

Figure Lengend Snippet: PNP supported growth of E. coli MG1655 (pSDP10). A indicates growth of MG1655 (pSDP10), MG1655 (pMMB206), and MG1655 cells in PNP-containing minimal medium. Closed (growth) and open (PNP) circles represent growth and PNP concentration in culture medium containing MG1655 (pSDP10). Similar parameters are indicated with closed (growth) and open (PNP) squares for MG1655 (pMMB206) and closed (growth) and open (PNP) rhombuses for MG1655 cultures. Proteins extracted from MG1655 (pSDP10) cells grown in the presence of normal and 14C-labeled PNP were analyzed by SDS-PAGE, and incorporation of 14C into proteins is shown in the corresponding autoradiogram (B). RNA extracted from similarly grown cultures and the corresponding autoradiogram are shown in C. The intense sharp signal shown by the arrow indicates incorporation of 14C into 5S rRNA. D indicates a decrease in concentration of PNP and concomitant release of stoichiometric amounts of nitrite in resting cells of E. coli (pSDP10). HPLC profiles showing the time-dependent decrease of PNP in the culture medium and the appearance of nitrocatechol (4.5 min) and benzenetriol (8.3 min) are shown in E and F. AU, absorbance units; ND, not detected.

Article Snippet: Probe Design The Agilent Custom Gene Expression E. coli MG1655 8 × 15K array (GT_CAT_11; AMADID number 019439) designed by Genotypic Technology Pvt.

Techniques: Concentration Assay, Labeling, SDS Page

The Orf306-dependent induction of the hca and mhp operons. A, heat map showing expression of the hca and mhp operons at 0, 1.5, and 3.0 h after induction of orf306. The portion of the two-dimensional gel showing Orf306-specific induction of HcaR and MhpA proteins is shown in B. The quantification (qPCR) of mhpA-, mhpR-, hcaE-, and hcaR-specific transcripts under similar growth conditions is shown in C with the error bars representing the S.D. Growth of the MG1655 (pDS10) (●) and hcaE (■), mhpA (▴), and mhpR (♦) mutants in PNP-containing minimal medium is shown in D. E represents agarose gel pictures indicating deletion of hcaE, mhpA, and mhpR genes. The PNP-dependent growth of MG1655 (pDS10) (●) and paaA (■) and maoA (▴) mutants (F) and an agarose gel showing the deletion of the paaA and maoA genes (G) are shown.

Journal: The Journal of Biological Chemistry

Article Title: The Organophosphate Degradation ( opd ) Island-borne Esterase-induced Metabolic Diversion in Escherichia coli and Its Influence on p -Nitrophenol Degradation *

doi: 10.1074/jbc.M115.661249

Figure Lengend Snippet: The Orf306-dependent induction of the hca and mhp operons. A, heat map showing expression of the hca and mhp operons at 0, 1.5, and 3.0 h after induction of orf306. The portion of the two-dimensional gel showing Orf306-specific induction of HcaR and MhpA proteins is shown in B. The quantification (qPCR) of mhpA-, mhpR-, hcaE-, and hcaR-specific transcripts under similar growth conditions is shown in C with the error bars representing the S.D. Growth of the MG1655 (pDS10) (●) and hcaE (■), mhpA (▴), and mhpR (♦) mutants in PNP-containing minimal medium is shown in D. E represents agarose gel pictures indicating deletion of hcaE, mhpA, and mhpR genes. The PNP-dependent growth of MG1655 (pDS10) (●) and paaA (■) and maoA (▴) mutants (F) and an agarose gel showing the deletion of the paaA and maoA genes (G) are shown.

Article Snippet: Probe Design The Agilent Custom Gene Expression E. coli MG1655 8 × 15K array (GT_CAT_11; AMADID number 019439) designed by Genotypic Technology Pvt.

Techniques: Expressing, Two-Dimensional Gel Electrophoresis, Agarose Gel Electrophoresis

Orf306-induced metabolic diversion in MG1655 (pSDP10). Heat maps represent differential expression of genes encoding glycolysis, glyoxylate, and TCA cycle enzymes at 0, 1.5, and 3.0 h. The green arrows represent down-regulated pathways. The up-regulated pathways are shown with red arrows. Up-regulation of the phenylpropionate pathway and down-regulation of glycolysis are shown with dotted green and red arrows, respectively. Quantitative PCR results showing either an Orf306-dependent decrease (pfkA, eno, and acnA) or increase (glcB, glcC, and prpB) in the concentration of specific mRNAs are inserted at places showing the corresponding enzyme reactions with the error bars representing the S.D. The two-dimensional gel portions indicate Orf306-dependent induction of MhpA, HcaR, GlcC, PrpB, and SdhA. Eno, enolase; PEP, phosphoenolpyruvate.

Journal: The Journal of Biological Chemistry

Article Title: The Organophosphate Degradation ( opd ) Island-borne Esterase-induced Metabolic Diversion in Escherichia coli and Its Influence on p -Nitrophenol Degradation *

doi: 10.1074/jbc.M115.661249

Figure Lengend Snippet: Orf306-induced metabolic diversion in MG1655 (pSDP10). Heat maps represent differential expression of genes encoding glycolysis, glyoxylate, and TCA cycle enzymes at 0, 1.5, and 3.0 h. The green arrows represent down-regulated pathways. The up-regulated pathways are shown with red arrows. Up-regulation of the phenylpropionate pathway and down-regulation of glycolysis are shown with dotted green and red arrows, respectively. Quantitative PCR results showing either an Orf306-dependent decrease (pfkA, eno, and acnA) or increase (glcB, glcC, and prpB) in the concentration of specific mRNAs are inserted at places showing the corresponding enzyme reactions with the error bars representing the S.D. The two-dimensional gel portions indicate Orf306-dependent induction of MhpA, HcaR, GlcC, PrpB, and SdhA. Eno, enolase; PEP, phosphoenolpyruvate.

Article Snippet: Probe Design The Agilent Custom Gene Expression E. coli MG1655 8 × 15K array (GT_CAT_11; AMADID number 019439) designed by Genotypic Technology Pvt.

Techniques: Expressing, Real-time Polymerase Chain Reaction, Concentration Assay, Two-Dimensional Gel Electrophoresis

Propionate-dependent induction of hcaR and mhpR genes. The lacZ-negative strains of MG1655 containing promoter test vector pMP220 and hcaR-, mhpR-, and mhpA-lacZ fusions were grown either on a propionate + X-gal (A) or a glucose + X-gal plate (B). The quantification of promoter activity for propionate- and glucose-grown cultures is shown in C and D, respectively, with the error bars representing the S.D. The Orf306-dependent induction of the hcaR, mhpR, and mhpA genes in MG1655 (pSDP10) cells is shown in E and F, respectively.

Journal: The Journal of Biological Chemistry

Article Title: The Organophosphate Degradation ( opd ) Island-borne Esterase-induced Metabolic Diversion in Escherichia coli and Its Influence on p -Nitrophenol Degradation *

doi: 10.1074/jbc.M115.661249

Figure Lengend Snippet: Propionate-dependent induction of hcaR and mhpR genes. The lacZ-negative strains of MG1655 containing promoter test vector pMP220 and hcaR-, mhpR-, and mhpA-lacZ fusions were grown either on a propionate + X-gal (A) or a glucose + X-gal plate (B). The quantification of promoter activity for propionate- and glucose-grown cultures is shown in C and D, respectively, with the error bars representing the S.D. The Orf306-dependent induction of the hcaR, mhpR, and mhpA genes in MG1655 (pSDP10) cells is shown in E and F, respectively.

Article Snippet: Probe Design The Agilent Custom Gene Expression E. coli MG1655 8 × 15K array (GT_CAT_11; AMADID number 019439) designed by Genotypic Technology Pvt.

Techniques: Plasmid Preparation, Activity Assay