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microgrid ii microarray spotter  (Zinsser Analytic)

 
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    Zinsser Analytic microgrid ii microarray spotter
    Biotype and genome location of ncRNAs from the neuro-ncRNA <t>microarray.</t> ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”
    Microgrid Ii Microarray Spotter, supplied by Zinsser Analytic, 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/microgrid ii microarray spotter/product/Zinsser Analytic
    Average 90 stars, based on 1 article reviews
    microgrid ii microarray spotter - by Bioz Stars, 2026-03
    90/100 stars

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    1) Product Images from "Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases"

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    Journal: RNA

    doi: 10.1261/rna.047225.114

    Biotype and genome location of ncRNAs from the neuro-ncRNA microarray. ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”
    Figure Legend Snippet: Biotype and genome location of ncRNAs from the neuro-ncRNA microarray. ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”

    Techniques Used: Microarray

    Comparison of expression analysis between Northern blot (black bars) and microarray analysis (gray bars) of 14 randomly chosen ncRNAs. ( A ) Expression changes of ncRNAs between brain and muscle tissues. ( B ) Expression changes of ncRNAs between brain and liver tissues. Candidate IDs are indicated on top . Details are listed in Supplemental Table 2. Fold changes from Northern blot analysis were quantified by using ImageQuant 8.1 (GE Healthcare).
    Figure Legend Snippet: Comparison of expression analysis between Northern blot (black bars) and microarray analysis (gray bars) of 14 randomly chosen ncRNAs. ( A ) Expression changes of ncRNAs between brain and muscle tissues. ( B ) Expression changes of ncRNAs between brain and liver tissues. Candidate IDs are indicated on top . Details are listed in Supplemental Table 2. Fold changes from Northern blot analysis were quantified by using ImageQuant 8.1 (GE Healthcare).

    Techniques Used: Comparison, Expressing, Northern Blot, Microarray

    Differential expression analysis of ncRNAs from selected brain regions of mouse models for voltage-gated calcium channel activity compared with wild type. ( A ) Cacnb4 mutant mouse: cerebellum. ( B ) Ca V 1.3 −/− : hippocampus. ( C ) Ca V 1.3 −/− : striatum. Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to wild-type controls in microarray experiments. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( D ) Venn diagram illustrating the overlap of differentially expressed candidates between the models analyzed. ( E ) Fold change and annotation of ncRNA candidates highlighted in D .
    Figure Legend Snippet: Differential expression analysis of ncRNAs from selected brain regions of mouse models for voltage-gated calcium channel activity compared with wild type. ( A ) Cacnb4 mutant mouse: cerebellum. ( B ) Ca V 1.3 −/− : hippocampus. ( C ) Ca V 1.3 −/− : striatum. Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to wild-type controls in microarray experiments. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( D ) Venn diagram illustrating the overlap of differentially expressed candidates between the models analyzed. ( E ) Fold change and annotation of ncRNA candidates highlighted in D .

    Techniques Used: Quantitative Proteomics, Activity Assay, Mutagenesis, Expressing, Microarray

    Differential expression of ncRNAs from cortices of a triple-transgenic (3xTG) mouse model for Alzheimer's disease compared with wild-type controls at the age of 3, 10, and 20 mo, respectively. ( A ) Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to their wild-type controls in microarray experiments. The experiments are illustrated from left to right : 3-, 10-, and 20-mo-old mice. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( B ) Venn diagram illustrating the overlap of differentially expressed candidates between the different age groups. ( C ) Fold change and annotation of ncRNA candidates highlighted in B .
    Figure Legend Snippet: Differential expression of ncRNAs from cortices of a triple-transgenic (3xTG) mouse model for Alzheimer's disease compared with wild-type controls at the age of 3, 10, and 20 mo, respectively. ( A ) Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to their wild-type controls in microarray experiments. The experiments are illustrated from left to right : 3-, 10-, and 20-mo-old mice. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( B ) Venn diagram illustrating the overlap of differentially expressed candidates between the different age groups. ( C ) Fold change and annotation of ncRNA candidates highlighted in B .

    Techniques Used: Quantitative Proteomics, Transgenic Assay, Expressing, Microarray

    Differentially expressed snoRNAs in young 3xTG AD mice. ( A ) Candidate e307: sequence similarity of mouse (mm9 assembly) to the human (hg19 assembly) snoRNA homologs (located on chromosome 5), and ( left ) predicted secondary structure illustrated by VARNA ( http://varna.lri.fr/ ). ( Right ) Northern blot analysis of e307 from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. ( B ) Candidate e470: genome positions of the two (red and green bars) potential loci of transcription (on chromosome 5), which differ by a single SNP (indicated in bold). Sequence similarity of HBII-336 and MBII-336; ( left ) predicted secondary structure illustrated by VARNA. ( Right ) Northern blot analysis from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. C/D boxes are illustrated in red and sequences targeted by the oligonucleotide from the microarray e307 and e470, respectively, are highlighted in blue.
    Figure Legend Snippet: Differentially expressed snoRNAs in young 3xTG AD mice. ( A ) Candidate e307: sequence similarity of mouse (mm9 assembly) to the human (hg19 assembly) snoRNA homologs (located on chromosome 5), and ( left ) predicted secondary structure illustrated by VARNA ( http://varna.lri.fr/ ). ( Right ) Northern blot analysis of e307 from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. ( B ) Candidate e470: genome positions of the two (red and green bars) potential loci of transcription (on chromosome 5), which differ by a single SNP (indicated in bold). Sequence similarity of HBII-336 and MBII-336; ( left ) predicted secondary structure illustrated by VARNA. ( Right ) Northern blot analysis from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. C/D boxes are illustrated in red and sequences targeted by the oligonucleotide from the microarray e307 and e470, respectively, are highlighted in blue.

    Techniques Used: Sequencing, Northern Blot, Microarray



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    microgrid ii microarray spotter  (Zinsser Analytic)
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    Zinsser Analytic microgrid ii microarray spotter
    Biotype and genome location of ncRNAs from the neuro-ncRNA <t>microarray.</t> ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”
    Microgrid Ii Microarray Spotter, supplied by Zinsser Analytic, 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/microgrid ii microarray spotter/product/Zinsser Analytic
    Average 90 stars, based on 1 article reviews
    microgrid ii microarray spotter - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Biotype and genome location of ncRNAs from the neuro-ncRNA microarray. ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”

    Journal: RNA

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    doi: 10.1261/rna.047225.114

    Figure Lengend Snippet: Biotype and genome location of ncRNAs from the neuro-ncRNA microarray. ncRNAs are sorted by ncRNA biotype and genomic locations. Frequencies are illustrated in log 2 scale. Frequency of zero is indicated in gray. Strandness of ncRNAs is included in the biotype names (sense: “_SE,” antisense: “_AS”). Biotypes follow GENCODE/ENSEMBL annotation. Missing annotations are designated as “unknown.”

    Article Snippet: The neuro-ncRNA microarray was generated using the MicroGrid II Microarray Spotter (Zinsser Analytic).

    Techniques: Microarray

    Comparison of expression analysis between Northern blot (black bars) and microarray analysis (gray bars) of 14 randomly chosen ncRNAs. ( A ) Expression changes of ncRNAs between brain and muscle tissues. ( B ) Expression changes of ncRNAs between brain and liver tissues. Candidate IDs are indicated on top . Details are listed in Supplemental Table 2. Fold changes from Northern blot analysis were quantified by using ImageQuant 8.1 (GE Healthcare).

    Journal: RNA

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    doi: 10.1261/rna.047225.114

    Figure Lengend Snippet: Comparison of expression analysis between Northern blot (black bars) and microarray analysis (gray bars) of 14 randomly chosen ncRNAs. ( A ) Expression changes of ncRNAs between brain and muscle tissues. ( B ) Expression changes of ncRNAs between brain and liver tissues. Candidate IDs are indicated on top . Details are listed in Supplemental Table 2. Fold changes from Northern blot analysis were quantified by using ImageQuant 8.1 (GE Healthcare).

    Article Snippet: The neuro-ncRNA microarray was generated using the MicroGrid II Microarray Spotter (Zinsser Analytic).

    Techniques: Comparison, Expressing, Northern Blot, Microarray

    Differential expression analysis of ncRNAs from selected brain regions of mouse models for voltage-gated calcium channel activity compared with wild type. ( A ) Cacnb4 mutant mouse: cerebellum. ( B ) Ca V 1.3 −/− : hippocampus. ( C ) Ca V 1.3 −/− : striatum. Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to wild-type controls in microarray experiments. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( D ) Venn diagram illustrating the overlap of differentially expressed candidates between the models analyzed. ( E ) Fold change and annotation of ncRNA candidates highlighted in D .

    Journal: RNA

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    doi: 10.1261/rna.047225.114

    Figure Lengend Snippet: Differential expression analysis of ncRNAs from selected brain regions of mouse models for voltage-gated calcium channel activity compared with wild type. ( A ) Cacnb4 mutant mouse: cerebellum. ( B ) Ca V 1.3 −/− : hippocampus. ( C ) Ca V 1.3 −/− : striatum. Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to wild-type controls in microarray experiments. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( D ) Venn diagram illustrating the overlap of differentially expressed candidates between the models analyzed. ( E ) Fold change and annotation of ncRNA candidates highlighted in D .

    Article Snippet: The neuro-ncRNA microarray was generated using the MicroGrid II Microarray Spotter (Zinsser Analytic).

    Techniques: Quantitative Proteomics, Activity Assay, Mutagenesis, Expressing, Microarray

    Differential expression of ncRNAs from cortices of a triple-transgenic (3xTG) mouse model for Alzheimer's disease compared with wild-type controls at the age of 3, 10, and 20 mo, respectively. ( A ) Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to their wild-type controls in microarray experiments. The experiments are illustrated from left to right : 3-, 10-, and 20-mo-old mice. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( B ) Venn diagram illustrating the overlap of differentially expressed candidates between the different age groups. ( C ) Fold change and annotation of ncRNA candidates highlighted in B .

    Journal: RNA

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    doi: 10.1261/rna.047225.114

    Figure Lengend Snippet: Differential expression of ncRNAs from cortices of a triple-transgenic (3xTG) mouse model for Alzheimer's disease compared with wild-type controls at the age of 3, 10, and 20 mo, respectively. ( A ) Box plots represent fold changes of ncRNAs (colored data points), which showed significant changes in expression relative to their wild-type controls in microarray experiments. The experiments are illustrated from left to right : 3-, 10-, and 20-mo-old mice. Fold changes are illustrated in log 2 scale. Whiskers extend to ±1.5-fold of the interquartile range (IQR). Biotypes are designated by color code: miRNAs (red), snoRNA (orange), tRF (blue), other biotypes (green), and unknown biotype (gray). ( B ) Venn diagram illustrating the overlap of differentially expressed candidates between the different age groups. ( C ) Fold change and annotation of ncRNA candidates highlighted in B .

    Article Snippet: The neuro-ncRNA microarray was generated using the MicroGrid II Microarray Spotter (Zinsser Analytic).

    Techniques: Quantitative Proteomics, Transgenic Assay, Expressing, Microarray

    Differentially expressed snoRNAs in young 3xTG AD mice. ( A ) Candidate e307: sequence similarity of mouse (mm9 assembly) to the human (hg19 assembly) snoRNA homologs (located on chromosome 5), and ( left ) predicted secondary structure illustrated by VARNA ( http://varna.lri.fr/ ). ( Right ) Northern blot analysis of e307 from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. ( B ) Candidate e470: genome positions of the two (red and green bars) potential loci of transcription (on chromosome 5), which differ by a single SNP (indicated in bold). Sequence similarity of HBII-336 and MBII-336; ( left ) predicted secondary structure illustrated by VARNA. ( Right ) Northern blot analysis from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. C/D boxes are illustrated in red and sequences targeted by the oligonucleotide from the microarray e307 and e470, respectively, are highlighted in blue.

    Journal: RNA

    Article Title: Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

    doi: 10.1261/rna.047225.114

    Figure Lengend Snippet: Differentially expressed snoRNAs in young 3xTG AD mice. ( A ) Candidate e307: sequence similarity of mouse (mm9 assembly) to the human (hg19 assembly) snoRNA homologs (located on chromosome 5), and ( left ) predicted secondary structure illustrated by VARNA ( http://varna.lri.fr/ ). ( Right ) Northern blot analysis of e307 from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. ( B ) Candidate e470: genome positions of the two (red and green bars) potential loci of transcription (on chromosome 5), which differ by a single SNP (indicated in bold). Sequence similarity of HBII-336 and MBII-336; ( left ) predicted secondary structure illustrated by VARNA. ( Right ) Northern blot analysis from total RNA of cortices of 10-mo-old 3xTG mice compared with wild-type controls. C/D boxes are illustrated in red and sequences targeted by the oligonucleotide from the microarray e307 and e470, respectively, are highlighted in blue.

    Article Snippet: The neuro-ncRNA microarray was generated using the MicroGrid II Microarray Spotter (Zinsser Analytic).

    Techniques: Sequencing, Northern Blot, Microarray