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custom designed oligonucleotide microarrays  (Agilent technologies)


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    Structured Review

    Agilent technologies custom designed oligonucleotide microarrays
    The rectangular boxes represent the entire transcriptomes of C. elegans and P. pacificus genes assayed on our <t>microarrays,</t> and their area of overlap represents the set of 6,126 1∶1 orthologs present on microarrays of both the nematodes. The ovals represent the fraction of differentially expressed genes in each of the subsets. For the 1∶1 orthologs, we assessed the significance of overlap between the genes differentially expressed in response to a given pathogen using a 2×2 Fisher's exact test. Differences or similarities in survival characteristics of the two nematodes when exposed to the same bacteria are reflected in their respective transcriptional responses. (A) On B. thuringiensis DB27, which is highly lethal to C. elegans but not to P. pacificus , only 23 genes are common between the respective expression profiles of the two nematodes, this overlap being statistically not significant. (B) Similarly, S. aureus is more lethal to C. elegans than P. pacificus , and the overlap between the corresponding expression profiles is limited to just 6 orthologs. Although this overlap is statistically significant (p-value = 0.0002), the extent of overlap is too small to be biologically significant. (C) S. marcescens is lethal to both the nematodes and the extent and significance overlap between the orthologs differentially expressed in the corresponding expression profiles is also relatively high (443 common orthologs, p-value = 7.71E–37). (D) On the pathogen X. nematophila , the observed overlap between the expression profiles in the two nematodes is even higher, with 2,093 orthologs regulated in both nematodes (p-value = 6.92E–134).
    Custom Designed Oligonucleotide 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/product/custom-designed+oligonucleotide+microarray/pmc03461006-203-7-13
    Average 90 stars, based on 1 article reviews
    custom designed oligonucleotide microarrays - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "System Wide Analysis of the Evolution of Innate Immunity in the Nematode Model Species Caenorhabditis elegans and Pristionchus pacificus"

    Article Title: System Wide Analysis of the Evolution of Innate Immunity in the Nematode Model Species Caenorhabditis elegans and Pristionchus pacificus

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0044255

    The rectangular boxes represent the entire transcriptomes of C. elegans and P. pacificus genes assayed on our microarrays, and their area of overlap represents the set of 6,126 1∶1 orthologs present on microarrays of both the nematodes. The ovals represent the fraction of differentially expressed genes in each of the subsets. For the 1∶1 orthologs, we assessed the significance of overlap between the genes differentially expressed in response to a given pathogen using a 2×2 Fisher's exact test. Differences or similarities in survival characteristics of the two nematodes when exposed to the same bacteria are reflected in their respective transcriptional responses. (A) On B. thuringiensis DB27, which is highly lethal to C. elegans but not to P. pacificus , only 23 genes are common between the respective expression profiles of the two nematodes, this overlap being statistically not significant. (B) Similarly, S. aureus is more lethal to C. elegans than P. pacificus , and the overlap between the corresponding expression profiles is limited to just 6 orthologs. Although this overlap is statistically significant (p-value = 0.0002), the extent of overlap is too small to be biologically significant. (C) S. marcescens is lethal to both the nematodes and the extent and significance overlap between the orthologs differentially expressed in the corresponding expression profiles is also relatively high (443 common orthologs, p-value = 7.71E–37). (D) On the pathogen X. nematophila , the observed overlap between the expression profiles in the two nematodes is even higher, with 2,093 orthologs regulated in both nematodes (p-value = 6.92E–134).
    Figure Legend Snippet: The rectangular boxes represent the entire transcriptomes of C. elegans and P. pacificus genes assayed on our microarrays, and their area of overlap represents the set of 6,126 1∶1 orthologs present on microarrays of both the nematodes. The ovals represent the fraction of differentially expressed genes in each of the subsets. For the 1∶1 orthologs, we assessed the significance of overlap between the genes differentially expressed in response to a given pathogen using a 2×2 Fisher's exact test. Differences or similarities in survival characteristics of the two nematodes when exposed to the same bacteria are reflected in their respective transcriptional responses. (A) On B. thuringiensis DB27, which is highly lethal to C. elegans but not to P. pacificus , only 23 genes are common between the respective expression profiles of the two nematodes, this overlap being statistically not significant. (B) Similarly, S. aureus is more lethal to C. elegans than P. pacificus , and the overlap between the corresponding expression profiles is limited to just 6 orthologs. Although this overlap is statistically significant (p-value = 0.0002), the extent of overlap is too small to be biologically significant. (C) S. marcescens is lethal to both the nematodes and the extent and significance overlap between the orthologs differentially expressed in the corresponding expression profiles is also relatively high (443 common orthologs, p-value = 7.71E–37). (D) On the pathogen X. nematophila , the observed overlap between the expression profiles in the two nematodes is even higher, with 2,093 orthologs regulated in both nematodes (p-value = 6.92E–134).

    Techniques Used: Expressing

    Related Articles

    Hybridization:

    Article Title: Development, Characterization and Experimental Validation of a Cultivated Sunflower ( Helianthus annuus L.) Gene Expression Oligonucleotide Microarray
    Article Snippet: Using the same public Helianthus EST data set, plus 454 sequences from the HA89 inbred line transcriptome, a Helianthus gene reference assembly was built to conduct SNP discovery and to design an Illumina Infinium BeadChip for genotyping . .. However, the use of a longer probe format represents an advantage of the Agilent oligonucleotide microarrays over other technologies, because the longer oligonucleotides provide a higher hybridization stability for sequence mismatches; consequently, the longer oligonucleotides are more suitable for the analysis of highly polymorphic regions . .. In this work, we present the development of a comprehensive Sunflower Unigene Resource, its functional annotation and the design and validation of a custom sunflower oligonucleotide-based microarray for identification of key regulatory genes for molecular breeding and examination of concerted transcriptional responses such as those associated with leaf senescence.

    Sequencing:

    Article Title: Development, Characterization and Experimental Validation of a Cultivated Sunflower ( Helianthus annuus L.) Gene Expression Oligonucleotide Microarray
    Article Snippet: Using the same public Helianthus EST data set, plus 454 sequences from the HA89 inbred line transcriptome, a Helianthus gene reference assembly was built to conduct SNP discovery and to design an Illumina Infinium BeadChip for genotyping . .. However, the use of a longer probe format represents an advantage of the Agilent oligonucleotide microarrays over other technologies, because the longer oligonucleotides provide a higher hybridization stability for sequence mismatches; consequently, the longer oligonucleotides are more suitable for the analysis of highly polymorphic regions . .. In this work, we present the development of a comprehensive Sunflower Unigene Resource, its functional annotation and the design and validation of a custom sunflower oligonucleotide-based microarray for identification of key regulatory genes for molecular breeding and examination of concerted transcriptional responses such as those associated with leaf senescence.

    Gene Expression:

    Article Title: Striatal Molecular Signature of Subchronic Subthalamic Nucleus High Frequency Stimulation in Parkinsonian Rat
    Article Snippet: .. Thus, 12 Agilent oligonucleotide microarrays were used to compare the gene expression profiles of 6-OHDA, HFS, DOPA and DOPA/HFS groups. .. Microarray data were extracted and quantified with Feature extraction software (Agilent).

    Labeling:

    Article Title: Comparative genomic and transcriptomic analysis revealed genetic characteristics related to solvent formation and xylose utilization in Clostridium acetobutylicum EA 2018
    Article Snippet: The total RNA yield was quantified by spectrophotometric analysis (NanoDrop Technology, Cambridge, UK) and the quality was verified by gel electrophoresis. .. Agilent oligonucleotide microarrays technology was used for monochromic analysis, in which probes (size: 60 bp; three replicates for each ORF) from the two groups were labeled by incorporation of cyanine 3 (Cy3) (Agilent Technologies, Palo Alto, CA, USA). ..

    Article Title: ECAT11/L1td1 Is Enriched in ESCs and Rapidly Activated During iPSCGeneration, but It Is Dispensable for the Maintenance and Induction of Pluripotency
    Article Snippet: .. Total RNA from wild-type and ECAT11 EGFP/EGFP ESCs were labeled with Cy3, and were hybridized to oligonucleotide microarrays (Agilent) according to the manufacturer's protocol. ..

    Functional Assay:

    Article Title: Oxidative Nanopatterning of Titanium Surface Influences mRNA and MicroRNA Expression in Human Alveolar Bone Osteoblastic Cells
    Article Snippet: Briefly, 500 ng of the individual total RNA was employed to synthesize double-stranded cDNA and cyanine 3 (Cy3) CTP labeled complementary amplified RNA (cRNA) by means of the Agilent Linear Amplification Kit (Agilent), according to the manufacturer's instructions. .. By using Agilent human 4 × 44 K oligonucleotide microarrays (Agilent), cyanine-labeled complementary RNA was hybridized to microarrays in SureHyb chambers (Agilent) in a rotator oven at 65°C, for 17 h. Each array contained 44,000 oligonucleotide probes covering the entire human functional genome. .. The arrays were washed according to the manufacturer's instructions and scanned with an Agilent DNA Microarray scanner.

    other:

    Article Title: Correlation of mRNA and protein levels: Cell type-specific gene expression of cluster designation antigens in the prostate
    Article Snippet: As an external control, IHC and array data from MACS-sorted cells were compared to LCM cells from prostate stromal and luminal cells analyzed by hybridization to long-oligonucleotide microarrays (Agilent Corporation).



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    Image Search Results


    The relative transcriptional level of 10 selected genes determined by DNA microarray and qRT-PCR analyses were log 2 transformed, and the values were plotted against each other to evaluate their correlation. The genes analysed by qRT-PCR are listed in .

    Journal: PLoS ONE

    Article Title: Two Spx Regulators Modulate Stress Tolerance and Virulence in Streptococcus suis Serotype 2

    doi: 10.1371/journal.pone.0108197

    Figure Lengend Snippet: The relative transcriptional level of 10 selected genes determined by DNA microarray and qRT-PCR analyses were log 2 transformed, and the values were plotted against each other to evaluate their correlation. The genes analysed by qRT-PCR are listed in .

    Article Snippet: DNA microarray analysis was performed using an Agilent custom-designed oligonucleotide microarray.

    Techniques: Microarray, Quantitative RT-PCR, Transformation Assay

    Expression ratios of genes involved in oxidative stress response and virulence in the mutant strains relative to the WT strain by  microarray  analysis <xref ref-type= a ." width="100%" height="100%">

    Journal: PLoS ONE

    Article Title: Two Spx Regulators Modulate Stress Tolerance and Virulence in Streptococcus suis Serotype 2

    doi: 10.1371/journal.pone.0108197

    Figure Lengend Snippet: Expression ratios of genes involved in oxidative stress response and virulence in the mutant strains relative to the WT strain by microarray analysis a .

    Article Snippet: DNA microarray analysis was performed using an Agilent custom-designed oligonucleotide microarray.

    Techniques: Expressing, Mutagenesis, Microarray

    Array findings from prenatal single nucleotide polymorphism microarray on amniocytes (estimated 60% mosaicism). Image courtesy of LabCorp (Burlington, North Carolina, United States).

    Journal: Journal of Pediatric Genetics

    Article Title: Mosaic Trisomy 16 Associated with Left Lung Agenesis, Abnormal Left Arm, and Right Pulmonary Artery Stenosis: Expanding the Phenotype and Review of the Literature

    doi: 10.1055/s-0040-1721136

    Figure Lengend Snippet: Array findings from prenatal single nucleotide polymorphism microarray on amniocytes (estimated 60% mosaicism). Image courtesy of LabCorp (Burlington, North Carolina, United States).

    Article Snippet: The CMA on foreskin was performed on a custom designed oligonucleotide microarray (GenomeDx v5).

    Techniques: Microarray

    Array findings from postnatal single nucleotide polymorphism microarray on foreskin tissue (estimated 25–40% mosaicism). Image courtesy of GeneDx (Gaithersburg, Maryland, United States).

    Journal: Journal of Pediatric Genetics

    Article Title: Mosaic Trisomy 16 Associated with Left Lung Agenesis, Abnormal Left Arm, and Right Pulmonary Artery Stenosis: Expanding the Phenotype and Review of the Literature

    doi: 10.1055/s-0040-1721136

    Figure Lengend Snippet: Array findings from postnatal single nucleotide polymorphism microarray on foreskin tissue (estimated 25–40% mosaicism). Image courtesy of GeneDx (Gaithersburg, Maryland, United States).

    Article Snippet: The CMA on foreskin was performed on a custom designed oligonucleotide microarray (GenomeDx v5).

    Techniques: Microarray

    The rectangular boxes represent the entire transcriptomes of C. elegans and P. pacificus genes assayed on our microarrays, and their area of overlap represents the set of 6,126 1∶1 orthologs present on microarrays of both the nematodes. The ovals represent the fraction of differentially expressed genes in each of the subsets. For the 1∶1 orthologs, we assessed the significance of overlap between the genes differentially expressed in response to a given pathogen using a 2×2 Fisher's exact test. Differences or similarities in survival characteristics of the two nematodes when exposed to the same bacteria are reflected in their respective transcriptional responses. (A) On B. thuringiensis DB27, which is highly lethal to C. elegans but not to P. pacificus , only 23 genes are common between the respective expression profiles of the two nematodes, this overlap being statistically not significant. (B) Similarly, S. aureus is more lethal to C. elegans than P. pacificus , and the overlap between the corresponding expression profiles is limited to just 6 orthologs. Although this overlap is statistically significant (p-value = 0.0002), the extent of overlap is too small to be biologically significant. (C) S. marcescens is lethal to both the nematodes and the extent and significance overlap between the orthologs differentially expressed in the corresponding expression profiles is also relatively high (443 common orthologs, p-value = 7.71E–37). (D) On the pathogen X. nematophila , the observed overlap between the expression profiles in the two nematodes is even higher, with 2,093 orthologs regulated in both nematodes (p-value = 6.92E–134).

    Journal: PLoS ONE

    Article Title: System Wide Analysis of the Evolution of Innate Immunity in the Nematode Model Species Caenorhabditis elegans and Pristionchus pacificus

    doi: 10.1371/journal.pone.0044255

    Figure Lengend Snippet: The rectangular boxes represent the entire transcriptomes of C. elegans and P. pacificus genes assayed on our microarrays, and their area of overlap represents the set of 6,126 1∶1 orthologs present on microarrays of both the nematodes. The ovals represent the fraction of differentially expressed genes in each of the subsets. For the 1∶1 orthologs, we assessed the significance of overlap between the genes differentially expressed in response to a given pathogen using a 2×2 Fisher's exact test. Differences or similarities in survival characteristics of the two nematodes when exposed to the same bacteria are reflected in their respective transcriptional responses. (A) On B. thuringiensis DB27, which is highly lethal to C. elegans but not to P. pacificus , only 23 genes are common between the respective expression profiles of the two nematodes, this overlap being statistically not significant. (B) Similarly, S. aureus is more lethal to C. elegans than P. pacificus , and the overlap between the corresponding expression profiles is limited to just 6 orthologs. Although this overlap is statistically significant (p-value = 0.0002), the extent of overlap is too small to be biologically significant. (C) S. marcescens is lethal to both the nematodes and the extent and significance overlap between the orthologs differentially expressed in the corresponding expression profiles is also relatively high (443 common orthologs, p-value = 7.71E–37). (D) On the pathogen X. nematophila , the observed overlap between the expression profiles in the two nematodes is even higher, with 2,093 orthologs regulated in both nematodes (p-value = 6.92E–134).

    Article Snippet: For P. pacificus experiments, we used our custom designed oligonucleotide microarrays manufactured by Agilent Technologies, which contain ∼93,000 unique probes for the ∼23,000 P. pacificus predicted genes (NCBI GEO accession GPL14372, see for design details of custom microarrays).

    Techniques: Expressing