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  • 85
    Agilent technologies g2565aa g2565ab scanner
    G2565aa G2565ab Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565aa g2565ba microarray scanner system
    G2565aa G2565ba Microarray Scanner System, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 87/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565aa microarray scanner
    G2565aa Microarray Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 97/100, based on 237 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ba scanner
    G2565ba Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 94/100, based on 156 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ca scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ca Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 96/100, based on 84 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies microarray scanner g2565ba
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    Microarray Scanner G2565ba, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 92/100, based on 509 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Agilent technologies g2565ca microarray scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ca Microarray Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 99/100, based on 710 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ca scanner system
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ca Scanner System, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 93/100, based on 83 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ba array scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ba Array Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565aa scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565aa Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 26 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies agilent g2566aa scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    Agilent G2566aa Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ba microarray scanner system
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ba Microarray Scanner System, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565aa dna microarray scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565aa Dna Microarray Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies microarray g2565ba fluorescent scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    Microarray G2565ba Fluorescent Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    89
    Agilent technologies g2565aa array scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565aa Array Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 89/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies laser scanner g2565ca
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    Laser Scanner G2565ca, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565ca dna scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ca Dna Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 89/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Agilent technologies g2567aa microarray scanner system
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2567aa Microarray Scanner System, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies g2565aa fluorescence scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565aa Fluorescence Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    Agilent technologies g2565ba dna scanner
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
    G2565ba Dna Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies dna microarray scanner model g2565aa
    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent <t>G2565CA</t> High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.
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    Chromosome aneuploidy in L. infantum Sb2000.1 and Sb4000.4 antimony-resistant mutants. Log 2 -transformed Sb2000.1/WT expression ratios of the upregulated chromosome 1 ( A ), chromosome 11 ( B ) and chromosome 25 ( C ) and of the downregulated chromosome 9 ( D ), chromosome 12 ( E ) and chromosome 32 ( F ) plotted as a function of the location of <t>microarray</t> probes on each chromosomes. For each plot, the log 2 -transformed gene expression ratios of chromosome 30, which was equally expressed in both samples, are shown as a control (grey line). Quantitative Southern blot hybridizations of digested genomic <t>DNA</t> extracted from L. infantum WT (lane 1), Sb2000.1 (lane 2) and Sb4000.4 (lane 3) were performed to correlate gene expression modulation of entire chromosomes with the chromosome DNA copy number. The hybridization signal of LinJ30_V3.2990 was used for normalization. The hybridization signals were quantified using ImageQuant 5.2 (Molecular Dynamics) and the fold differences in DNA copy number of Sb2000.1 compared to WT are found below each blot.
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    Chromosome aneuploidy in L. infantum Sb2000.1 and Sb4000.4 antimony-resistant mutants. Log 2 -transformed Sb2000.1/WT expression ratios of the upregulated chromosome 1 ( A ), chromosome 11 ( B ) and chromosome 25 ( C ) and of the downregulated chromosome 9 ( D ), chromosome 12 ( E ) and chromosome 32 ( F ) plotted as a function of the location of <t>microarray</t> probes on each chromosomes. For each plot, the log 2 -transformed gene expression ratios of chromosome 30, which was equally expressed in both samples, are shown as a control (grey line). Quantitative Southern blot hybridizations of digested genomic <t>DNA</t> extracted from L. infantum WT (lane 1), Sb2000.1 (lane 2) and Sb4000.4 (lane 3) were performed to correlate gene expression modulation of entire chromosomes with the chromosome DNA copy number. The hybridization signal of LinJ30_V3.2990 was used for normalization. The hybridization signals were quantified using ImageQuant 5.2 (Molecular Dynamics) and the fold differences in DNA copy number of Sb2000.1 compared to WT are found below each blot.
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    Chromosome aneuploidy in L. infantum Sb2000.1 and Sb4000.4 antimony-resistant mutants. Log 2 -transformed Sb2000.1/WT expression ratios of the upregulated chromosome 1 ( A ), chromosome 11 ( B ) and chromosome 25 ( C ) and of the downregulated chromosome 9 ( D ), chromosome 12 ( E ) and chromosome 32 ( F ) plotted as a function of the location of <t>microarray</t> probes on each chromosomes. For each plot, the log 2 -transformed gene expression ratios of chromosome 30, which was equally expressed in both samples, are shown as a control (grey line). Quantitative Southern blot hybridizations of digested genomic <t>DNA</t> extracted from L. infantum WT (lane 1), Sb2000.1 (lane 2) and Sb4000.4 (lane 3) were performed to correlate gene expression modulation of entire chromosomes with the chromosome DNA copy number. The hybridization signal of LinJ30_V3.2990 was used for normalization. The hybridization signals were quantified using ImageQuant 5.2 (Molecular Dynamics) and the fold differences in DNA copy number of Sb2000.1 compared to WT are found below each blot.
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    Cancer cell AGR2/CD10 RNA expression levels. Levels were determined through <t>DNA</t> <t>microarray</t> analysis with signal intensity values on the y -axis. Indicated on the x -axis are G3 and G4 primary tumor cell types, L luminal, LNCaP, C4-2, CL1, DU145, PC3 cell lines, LuCaP35, LuCaP 49 xenografts. Except for DU145 and LuCaP 49, the expression pattern is either CD10 or AGR2.
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    Cancer cell AGR2/CD10 RNA expression levels. Levels were determined through <t>DNA</t> <t>microarray</t> analysis with signal intensity values on the y -axis. Indicated on the x -axis are G3 and G4 primary tumor cell types, L luminal, LNCaP, C4-2, CL1, DU145, PC3 cell lines, LuCaP35, LuCaP 49 xenografts. Except for DU145 and LuCaP 49, the expression pattern is either CD10 or AGR2.
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    Image Search Results


    Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent G2565CA High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.

    Journal: Gene expression patterns : GEP

    Article Title: Screen for Slit/Robo signaling in trunk neural cells reveals new players

    doi: 10.1016/j.gep.2018.01.002

    Figure Lengend Snippet: Microarray of Slit2 produced log ratios, expression and classification of genes. ( A ) Cartoon of a chicken embryo electroporation. In green we show the putative plasmid solution with fast green being injected inside the neural tube. And the ± shows the position of the electrodes when giving them the electric pulses necessary for the plasmid to enter cells in the NT. ( B ) Workflow and sample preparation and array processing. For the microarray we processed 6 Total RNA samples (1 Control, 2 experimental in duplicates) for gene expression. RNA quality and concentration was determined on the Agilent Bioanalyzer and NanoDrop spectrophotometer. One-color labeling reactions were prepared using the Agilent Two-Color Protocol (Version 6.6) with 400 ng total RNA input. ( C ) Log ratio values collected after microarray show significantly upregulated genes (red), significantly down regulated genes (green), and not differentially expressed (yellow). Control samples were labeled with Cy5 and Experimental sample labeled with Cy3. RNA Spike A mix was used for Cy3 (experimental) samples and RNA spike B mix was used for all Cy5 (Control) samples and scanned at 3 μM resolution on an Agilent G2565CA High Resolution Scanner. ( D ) Percentage of gene expression upon Slit2 gain of function in microarray. The bar graphed represents 37.3% down-regulation genes and 62.7% of incidents generated up-regulated genes of NCCs Slit2 GOF vs control.

    Article Snippet: Next, the labeled cRNA is fragmented and placed on the chicken 4×44K Gene Expression microarray and hybridized at 65 °C for ~17 h. Finally, the arrays are washed and scanned at 3 μM resolution on an Agilent G2565CA High Resolution Scanner.

    Techniques: Microarray, Produced, Expressing, Electroporation, Plasmid Preparation, Injection, Sample Prep, Concentration Assay, Spectrophotometry, Labeling, Generated

    Chromosome aneuploidy in L. infantum Sb2000.1 and Sb4000.4 antimony-resistant mutants. Log 2 -transformed Sb2000.1/WT expression ratios of the upregulated chromosome 1 ( A ), chromosome 11 ( B ) and chromosome 25 ( C ) and of the downregulated chromosome 9 ( D ), chromosome 12 ( E ) and chromosome 32 ( F ) plotted as a function of the location of microarray probes on each chromosomes. For each plot, the log 2 -transformed gene expression ratios of chromosome 30, which was equally expressed in both samples, are shown as a control (grey line). Quantitative Southern blot hybridizations of digested genomic DNA extracted from L. infantum WT (lane 1), Sb2000.1 (lane 2) and Sb4000.4 (lane 3) were performed to correlate gene expression modulation of entire chromosomes with the chromosome DNA copy number. The hybridization signal of LinJ30_V3.2990 was used for normalization. The hybridization signals were quantified using ImageQuant 5.2 (Molecular Dynamics) and the fold differences in DNA copy number of Sb2000.1 compared to WT are found below each blot.

    Journal: Nucleic Acids Research

    Article Title: Gene expression modulation is associated with gene amplification, supernumerary chromosomes and chromosome loss in antimony-resistant Leishmania infantum

    doi: 10.1093/nar/gkn1069

    Figure Lengend Snippet: Chromosome aneuploidy in L. infantum Sb2000.1 and Sb4000.4 antimony-resistant mutants. Log 2 -transformed Sb2000.1/WT expression ratios of the upregulated chromosome 1 ( A ), chromosome 11 ( B ) and chromosome 25 ( C ) and of the downregulated chromosome 9 ( D ), chromosome 12 ( E ) and chromosome 32 ( F ) plotted as a function of the location of microarray probes on each chromosomes. For each plot, the log 2 -transformed gene expression ratios of chromosome 30, which was equally expressed in both samples, are shown as a control (grey line). Quantitative Southern blot hybridizations of digested genomic DNA extracted from L. infantum WT (lane 1), Sb2000.1 (lane 2) and Sb4000.4 (lane 3) were performed to correlate gene expression modulation of entire chromosomes with the chromosome DNA copy number. The hybridization signal of LinJ30_V3.2990 was used for normalization. The hybridization signals were quantified using ImageQuant 5.2 (Molecular Dynamics) and the fold differences in DNA copy number of Sb2000.1 compared to WT are found below each blot.

    Article Snippet: Microarray data acquisition and analysis Detection of the Alexa Fluor 555 and Alexa Fluor 647 signals was performed on a G2565CA DNA microarray scanner (Agilent technologies) at a 5-μm resolution.

    Techniques: Transformation Assay, Expressing, Microarray, Southern Blot, Hybridization

    Cancer cell AGR2/CD10 RNA expression levels. Levels were determined through DNA microarray analysis with signal intensity values on the y -axis. Indicated on the x -axis are G3 and G4 primary tumor cell types, L luminal, LNCaP, C4-2, CL1, DU145, PC3 cell lines, LuCaP35, LuCaP 49 xenografts. Except for DU145 and LuCaP 49, the expression pattern is either CD10 or AGR2.

    Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

    Article Title: Prostate cancer cell phenotypes based on AGR2 and CD10 expression

    doi: 10.1038/modpathol.2012.238

    Figure Lengend Snippet: Cancer cell AGR2/CD10 RNA expression levels. Levels were determined through DNA microarray analysis with signal intensity values on the y -axis. Indicated on the x -axis are G3 and G4 primary tumor cell types, L luminal, LNCaP, C4-2, CL1, DU145, PC3 cell lines, LuCaP35, LuCaP 49 xenografts. Except for DU145 and LuCaP 49, the expression pattern is either CD10 or AGR2.

    Article Snippet: Probe labeling and hybridization was performed following the Agilent protocol, and fluorescent array images were collected using the Agilent DNA microarray scanner G2565BA.

    Techniques: RNA Expression, Microarray, Expressing

    Expression levels of AGR2 and CD10 in xenografts. As inferred from DNA microarray analysis, these levels are presented in histogram format (top). CY3 intensity values are indicated on the y -axis. Because of the lower values for CD10, a separate histogram for CD10 is included (bottom). Note the ~6-fold decrease in CD10 from LuCaP 96 to Lu CaP 96CR.

    Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

    Article Title: Prostate cancer cell phenotypes based on AGR2 and CD10 expression

    doi: 10.1038/modpathol.2012.238

    Figure Lengend Snippet: Expression levels of AGR2 and CD10 in xenografts. As inferred from DNA microarray analysis, these levels are presented in histogram format (top). CY3 intensity values are indicated on the y -axis. Because of the lower values for CD10, a separate histogram for CD10 is included (bottom). Note the ~6-fold decrease in CD10 from LuCaP 96 to Lu CaP 96CR.

    Article Snippet: Probe labeling and hybridization was performed following the Agilent protocol, and fluorescent array images were collected using the Agilent DNA microarray scanner G2565BA.

    Techniques: Expressing, Microarray

    Gene expression profiling of marker genes in differentiated and undifferentiated MCT samples. Heat map and hierarchical clustering of all samples analyzed by DNA microarray using probes referable to the transcripts identified by class prediction analysis. Red indicates up-regulated and green down-regulated genes relative to the mean expression in all samples. For display purposes, samples in each class (differentiated and undifferentiated) were clustered separately and arranged from differentiated (left, yellow) to undifferentiated (right, red). Genes were hierarchically clustered separately based on the Pearson correlation coefficients and average linkage clustering. Units of the bar legend: absolute values.

    Journal: PLoS ONE

    Article Title: Global Gene Expression Analysis of Canine Cutaneous Mast Cell Tumor: Could Molecular Profiling Be Useful for Subtype Classification and Prognostication?

    doi: 10.1371/journal.pone.0095481

    Figure Lengend Snippet: Gene expression profiling of marker genes in differentiated and undifferentiated MCT samples. Heat map and hierarchical clustering of all samples analyzed by DNA microarray using probes referable to the transcripts identified by class prediction analysis. Red indicates up-regulated and green down-regulated genes relative to the mean expression in all samples. For display purposes, samples in each class (differentiated and undifferentiated) were clustered separately and arranged from differentiated (left, yellow) to undifferentiated (right, red). Genes were hierarchically clustered separately based on the Pearson correlation coefficients and average linkage clustering. Units of the bar legend: absolute values.

    Article Snippet: Hybridized slides were scanned at 5 µm resolution using a G2565BA DNA microarray scanner (Agilent Technologies, Santa Clara, CA).

    Techniques: Expressing, Marker, Microarray