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microarray equipment biorobotics microgrid  (BioRobotics Ltd)

 
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    BioRobotics Ltd microarray equipment biorobotics microgrid
    Microarray Equipment Biorobotics Microgrid, supplied by BioRobotics Ltd, 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/microarray+printer+biorobotics+microgrid+ii/biorobotics+microgrid/us08911942-483-3-6
    Average 90 stars, based on 1 article reviews
    microarray equipment biorobotics microgrid - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Method for detecting a target nucleic acid comprising two portions using probes having a first portion complementary to the first portion of the target nucleic acid and a second portion substantially complementary to the second portion of the target nucleic acid
    Article Snippet: The probes were then spotted (i.e., printed) on Schott Nexterion® Slide E coated microarray slides using a Genomic Solutions® BioRobotics MicroGrid II according the MicroGrid manufacturer's directions.

    Article Title: Identification of a cis -regulatory element by transient analysis of co-ordinately regulated genes
    Article Snippet: Arabidopsis full genome 27 K oligo microarrays (Operon) were spotted onto epoxy coated slides (MWG) in a 150 mM phosphate buffer, pH 8.5, using a Biorobotics MicroGrid robot and Biorobotics 100 μM pins.

    Article Title: Rapid and sensitive identification of uropathogenic Escherichia coli using a surface-enhanced-Raman-scattering-based biochip.
    Article Snippet: A pin spotter (Biorobotics Microgrid II) was used to locally deposit droplets of a few nL of antibody solutions by contact on the freshly activated surface.

    Article Title: Compositions and methods for prognosis and treatment of prostate cancer
    Article Snippet: 20 μM of each probe were dissolved in 2×SSC+0.0035% SDS and spotted in triplicate on Schott Nexterion® Slide E-coated microarray slides using a Genomic Solutions® BioRobotics MicroGrid II, according the MicroGrid manufacturer's directions.

    Article Title: Non-invasive bat species identification from mixed-species samples using a microarray
    Article Snippet: 1 Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA 2 Science and Engineering Division, Portland Community College, Portland, OR 97280, USA 3 Department of Biological Sciences and Institute of the Environment and Sustainability, Western Michigan University, Kalamazoo, MI 49008, USA Received: 3 March 2016 / Accepted: 8 September 2016 © Springer Science+Business Media Dordrecht 2016 Non-invasive bat species identification from mixed-species samples using a microarray

    Article Title: Oxidative stress, mitochondrial damage, and cores in muscle from calsequestrin-1 knockout mice.
    Article Snippet: Briefly, each oligonucleotide is spotted by a robotic station Biorobotics Microgrid II, in one replicate on a MICROMAX glass slide SuperChip I (Cat No MPS696) provided by PerkinElmer Life Sciences Inc.

    Modification:

    Article Title: Automated Printing of Electrochemical Immunoassay Microarrays: Studies of Conditions Affecting Alkaline Phosphatase Enzyme Label Activity
    Article Snippet: Microarray printing of components of an enzyme-linked immunosorbant assay (ELISA) is attractive for constructing miniaturized platforms to simultaneously and quantitatively analyze multiple chemical species in clinical, environmental, and forensic applications.. A truncated version of an electrochemical ELISA was used to address a major challenge of this approach, namely the effect of evaporation on assay activity.. An antibodyalkaline phosphatase conjugate (Ab-AP) was printed with a microarrayer onto an N-hydroxysuccinimide-ester-terminated selfassembled monolayer on gold.

    Microarray:

    Article Title: The trypanosome transcriptome is remodelled during differentiation but displays limited responsiveness within life stages
    Article Snippet: Oligonucleotides were manufactured by Illumina (Invitrogen) and included a 5' amino modification for attachment to Codelink activated slides (GE Healthcare). .. Arrays were printed using a BioRobotics Microgrid (Genomic Solutions) equipped with 16 NanoPins (Matrix Technology Corporation) in the Centre for Microarray Resources, Department of Pathology, University of Cambridge. .. Slides were prepared, washed and dried according to the manufacturer's instructions (GE Healthcare).



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    microarray printer biorobotics microgrid ii  (BioRobotics Ltd)
    90
    BioRobotics Ltd microarray printer biorobotics microgrid ii
    Testing the limits of NRF2 binding. Systematic multivariate ARE results by protein binding <t>microarray</t> for NRF2-MAFG heterodimer are shown. Tolerance for sequence variation was studied for positions 1–3 (white), 6–8 (grey) and 9–11 (dark grey) ( A ) and positions 1, 5 and 11 (seed sequences are shown in grey) ( B ). Results are depicted as measured binding relative to NQO1.ARE binding (black) (mean ± S.E.M., n = 45).
    Microarray Printer Biorobotics Microgrid Ii, supplied by BioRobotics Ltd, 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/microarray+printer+biorobotics+microgrid+ii/microgrid+ii+microarray+robot/pmc04770247-73-24-26
    Average 90 stars, based on 1 article reviews
    microarray printer biorobotics microgrid ii - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

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    Testing the limits of NRF2 binding. Systematic multivariate ARE results by protein binding microarray for NRF2-MAFG heterodimer are shown. Tolerance for sequence variation was studied for positions 1–3 (white), 6–8 (grey) and 9–11 (dark grey) ( A ) and positions 1, 5 and 11 (seed sequences are shown in grey) ( B ). Results are depicted as measured binding relative to NQO1.ARE binding (black) (mean ± S.E.M., n = 45).

    Journal: Nucleic Acids Research

    Article Title: The Effects of Sequence Variation on Genome-wide NRF2 Binding—New Target Genes and Regulatory SNPs

    doi: 10.1093/nar/gkw052

    Figure Lengend Snippet: Testing the limits of NRF2 binding. Systematic multivariate ARE results by protein binding microarray for NRF2-MAFG heterodimer are shown. Tolerance for sequence variation was studied for positions 1–3 (white), 6–8 (grey) and 9–11 (dark grey) ( A ) and positions 1, 5 and 11 (seed sequences are shown in grey) ( B ). Results are depicted as measured binding relative to NQO1.ARE binding (black) (mean ± S.E.M., n = 45).

    Article Snippet: The dilutions were dispensed in a 384-well plate (polypropylene plate No 267462, Nunc, N.Y, USA) and printed onto the avidin-coated glass slides with a microarray printer (BioRobotics MicroGrid II, BioRobotics Ltd, Cambridge, UK).

    Techniques: Binding Assay, Protein Binding, Microarray, Sequencing

    A SNP in FTL promoter has drastic effects of NRF2 binding and transcriptional activation. ( A ) A promoter analysis of the FTL gene at chr19 showing the location of experimentally verified NRF2 binding ARE together with dbSNP (v138) and ENCODE ChIP-seq data. ChIP-seq track displays combined MAFF and MAFK binding signals in H1-hESC (MAFK), K562 (MAFF, MAFK), HeLa-S3 (MAFK), HepG (MAFF, MAFK) and IMR90 (MAFK) cell lines. ( B ) Detailed view showing FTL ARE sequence and the SNP (rs113067944, A→C) position. ( C ) Protein binding microarray results for FTL.ARE.A and the SNP bearing FTL.ARE.C. Results are calculated as measured binding relative to NQO1.ARE binding (mean ± S.E.M, n = 39.). Scramble oligonucleotides served as negative control. ( D ) HEK-293T cells were transfected with NQO1-ARE and FTL-ARE bearing either allele A or allele C with and without NRF2 -expressing plasmids. Twenty-four h after transfection cells were treated with NRF2 inducer (L-SFN) for 16 h followed by luciferase activity measurements. An empty pGL3 promoter vector served as control and activities were normalized to β-galactosidase activity. Results are shown relative to control (mean± S.E.M, n = 4).

    Journal: Nucleic Acids Research

    Article Title: The Effects of Sequence Variation on Genome-wide NRF2 Binding—New Target Genes and Regulatory SNPs

    doi: 10.1093/nar/gkw052

    Figure Lengend Snippet: A SNP in FTL promoter has drastic effects of NRF2 binding and transcriptional activation. ( A ) A promoter analysis of the FTL gene at chr19 showing the location of experimentally verified NRF2 binding ARE together with dbSNP (v138) and ENCODE ChIP-seq data. ChIP-seq track displays combined MAFF and MAFK binding signals in H1-hESC (MAFK), K562 (MAFF, MAFK), HeLa-S3 (MAFK), HepG (MAFF, MAFK) and IMR90 (MAFK) cell lines. ( B ) Detailed view showing FTL ARE sequence and the SNP (rs113067944, A→C) position. ( C ) Protein binding microarray results for FTL.ARE.A and the SNP bearing FTL.ARE.C. Results are calculated as measured binding relative to NQO1.ARE binding (mean ± S.E.M, n = 39.). Scramble oligonucleotides served as negative control. ( D ) HEK-293T cells were transfected with NQO1-ARE and FTL-ARE bearing either allele A or allele C with and without NRF2 -expressing plasmids. Twenty-four h after transfection cells were treated with NRF2 inducer (L-SFN) for 16 h followed by luciferase activity measurements. An empty pGL3 promoter vector served as control and activities were normalized to β-galactosidase activity. Results are shown relative to control (mean± S.E.M, n = 4).

    Article Snippet: The dilutions were dispensed in a 384-well plate (polypropylene plate No 267462, Nunc, N.Y, USA) and printed onto the avidin-coated glass slides with a microarray printer (BioRobotics MicroGrid II, BioRobotics Ltd, Cambridge, UK).

    Techniques: Binding Assay, Activation Assay, ChIP-sequencing, Sequencing, Protein Binding, Microarray, Negative Control, Transfection, Expressing, Luciferase, Activity Assay, Plasmid Preparation, Control