microgrid ii microarray spotter (Zinsser Analytic)
90
Structured Review
Zinsser Analytic
microgrid ii microarray spotter
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/product/microgrid+ii+contact+microarrayer/microgrid+ii+microarrayer/pmc03384982-27-30-34
Average 90 stars, based on 1 article reviews
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/product/microgrid+ii+contact+microarrayer/microgrid+ii+microarrayer/pmc03384982-27-30-34
Average 90 stars, based on 1 article reviews
microgrid ii microarray spotter - by Bioz Stars,
2026-10
90/100 stars
Images
1) Product Images from "Expression Profiling of a Heterogeneous Population of ncRNAs Employing a Mixed DNA/LNA Microarray"
Article Title: Expression Profiling of a Heterogeneous Population of ncRNAs Employing a Mixed DNA/LNA Microarray
Journal: Journal of Nucleic Acids
doi: 10.1155/2012/283560
Figure Legend Snippet: Self-self hybridization at 56°C of 5 μ g (per dye) of labeled total mouse brain RNA. Diagrams of average intensity values show filtered results in logarithmic scale. The y axis represents values of AlexaFluor3 dye measurement at 532 nm, and the x axis represents values of AlexaFluor5 dye measurement at 635 nm. Red spots represent all signals from LNA and DNA probes spotted on the microarray slide. (a, c) Detection of MiR-9 (yellow spots, black arrow) and miR-9* (yellow spots, white arrow) with LNA probes. (b, d) Detection of snoRNAs (yellow spots) with antisense DNA probes (including mismatch probes in (d)). Sense DNA probes signals were below detection levels and thus filtered out. (a, b) RNA labeling using the protocol described by manufacturer. (c, d) Modified RNA labeling (see ).
Techniques Used: Hybridization, Labeling, Microarray, Modification
Figure Legend Snippet: Self-self hybridization at 56°C of 1 μ g (per dye) of labeled total mouse brain RNA. Diagrams of average intensity values show filtered results in logarithmic scale. The y axis represents values of AlexaFluor 3 dye measurement at 532 nm, and the x axis represents values of AlexaFluor5 dye measurement at 635 nm. Red spots represent all signals from LNA and DNA probes spotted on the microarray slide. Detection of (a) tRNAs (yellow spots) and (b) 7SK RNA (yellow spots) with antisense DNA probes (including mismatch and deletion probes). Sense DNA probes were below detection levels and thus filtered out. (c) Diagram showing mean intensity values ( y axis) of DNA probes for detection of highly structured ncRNAs.
Techniques Used: Hybridization, Labeling, Microarray
Figure Legend Snippet: Self-self hybridization at 64°C of 2 μ g (per dye) of labeled total mouse brain RNA. Diagrams of average intensity values show filtered results in logarithmic scale. The y axis represents values of AlexaFluor3 dye measurement at 532 nm, and the x axis represents values of AlexaFluor5 dye measurement at 635 nm. Red spots represent all signals from LNA and DNA probes spotted on the microarray slide. (a) Detection of snoRNAs (yellow spots) with antisense DNA probes. (b) Detection of miR-9 (yellow spots, black arrows) and miR-9* (yellow spots, white arrow). Sense DNA probes were below detection levels and filtered out. (c) Diagram showing mean intensity values ( y axis) of all antisense DNA probes detecting snoRNAs.
Techniques Used: Hybridization, Labeling, Microarray
Figure Legend Snippet: Self-self hybridization at 64°C of 2 μ g (per dye) of labeled total mouse brain RNA. Diagrams of average intensity values show filtered results in logarithmic scale. The y axis represents values of AlexaFluor3 dye measurement at 532 nm, and the x axis represents values of AlexaFluor5 dye measurement at 635 nm. Red spots represent all signals from LNA and DNA probes spotted on the microarray slide. (a) Detection of snoZ39 (yellow spots) with antisense DNA probes (black arrow, blow up) and one nucleotide mismatch DNA probe (white arrow, blow up). (b) Diagram showing on the y axis the percentage of mean detection value of the antisense probe SNOZ39−6–60MM1 and the one nucleotide mismatch probe SNOZ39−6–60MM1. (c) Diagram showing the mean intensity values ( y axis) of the antisense probes of one (MM1) and two (MM2) nucleotide mismatch probes for 7SK RNA and SNORD55.
Techniques Used: Hybridization, Labeling, Microarray
Figure Legend Snippet: (a) Heat map showing differential expression between brain and mouse embryonic stem cells of ncRNAs spotted on the DNA-LNA microarray. Up- and downregulation of ncRNAs in brain are indicated with red or green color, respectively. Only differential expression of at least two folds is indicated. (b) Northern blot showing expression of SNORD55 and SNORA71 in mouse embryonic stem cells and mouse brain. Ten micrograms of total RNA were used, and 5.8S rRNA was used as a loading control.
Techniques Used: Quantitative Proteomics, Microarray, Northern Blot, Expressing, Control
Figure Legend Snippet: Real-time PCR verification of differential expression of selected ncRNAs captured by DNA and LNA probes on the DNA/LNA microarray platform. Results are represented as relative expression levels between mouse ES cells and mouse brain. Data are shown as mean ± SEM; n = 5; * P < 0.05; ** P < 0.01, *** P < 0.005 significantly different from mES cells by Student t -test.
Techniques Used: Real-time Polymerase Chain Reaction, Quantitative Proteomics, Microarray, Expressing
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