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microrna microarray analysis  (Agilent technologies)


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    Structured Review

    Agilent technologies microrna microarray analysis
    Microrna Microarray Analysis, 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/microrna+microarray+analysis/pmc09151726-45-1-0
    Average 90 stars, based on 1 article reviews
    microrna microarray analysis - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: A novel TGFbeta/TGILR axis mediates crosstalk between cancer-associated fibroblasts and tumor cells to drive gastric cancer progression
    Article Snippet: .. Thus, a high-throughput Agilent microRNA profile microarray was performed to identify the differentially expressed microRNAs after TARBP2 overexpression. ..

    Article Title: Intra-Platform Repeatability and Inter-Platform Comparability of MicroRNA Microarray Technology
    Article Snippet: .. Five commercially available microRNA microarray platforms; Agilent Technologies (Santa Clara, CA), Ambion (Austin, TX), Exiqon (Vedbaek, Denmark), Invitrogen (Carlsbad, CA), and Toray (Tokyo, Japan) were tested in this study. ..

    Article Title: Pre-processing and differential expression analysis of Agilent microRNA arrays using the AgiMicroRna Bioconductor library
    Article Snippet: .. Pradervand et al. [ ] carried out a similar investigation using the Agilent microRNA microarray platform and the summarized TGS obtained with the AFE image analysis software provided by the vendor. ..

    Article Title: Pre-processing and differential expression analysis of Agilent microRNA arrays using the AgiMicroRna Bioconductor library
    Article Snippet: .. For each microRNA, the Agilent microRNA microarray platform makes measurements with a number of different oligonucleotide probes that are replicated a number of times across the array surface. .. These replicate signals are summarized into a total gene signal (TGS) with the proprietary Agilent Feature Extraction (AFE) image analysis algorithm [ ], which makes use of the background corrected signals.

    Article Title: Clear cell renal cell carcinoma associated microRNA expression signatures identified by an integrated bioinformatics analysis
    Article Snippet: .. GSE12105 , [ ] , Agilent Human microRNA Microarray , 490 , 12 , 12 , t-test. .. GSE16441 , [ ] , Agilent Human microRNA Microarray , 851 , 8 , 8 , SAM.

    Article Title: Clear cell renal cell carcinoma associated microRNA expression signatures identified by an integrated bioinformatics analysis
    Article Snippet: GSE12105 , [ ] , Agilent Human microRNA Microarray , 490 , 12 , 12 , t-test. .. GSE16441 , [ ] , Agilent Human microRNA Microarray , 851 , 8 , 8 , SAM. ..

    Article Title: MicroRNA-34a modulates genes involved in cellular motility and oxidative phosphorylation in neural precursors derived from human umbilical cord mesenchymal stem cells
    Article Snippet: .. We subjected WJ-MSCs into neurogenesis by a published protocol, and the miRNome patterns of WJ-MSCs and their neuronal progenitors (day 9 after differentiation) were analyzed by the Agilent microRNA microarray. ..

    Article Title: A novel TGFbeta/TGILR axis mediates crosstalk between cancer-associated fibroblasts and tumor cells to drive gastric cancer progression.
    Article Snippet: .. Thus, a high-throughput Agilent microRNA profile microarray was performed to identify the differentially expressed microRNAs after TARBP2 overexpression. ..

    Over Expression:

    Article Title: A novel TGFbeta/TGILR axis mediates crosstalk between cancer-associated fibroblasts and tumor cells to drive gastric cancer progression
    Article Snippet: .. Thus, a high-throughput Agilent microRNA profile microarray was performed to identify the differentially expressed microRNAs after TARBP2 overexpression. ..

    Article Title: A novel TGFbeta/TGILR axis mediates crosstalk between cancer-associated fibroblasts and tumor cells to drive gastric cancer progression.
    Article Snippet: .. Thus, a high-throughput Agilent microRNA profile microarray was performed to identify the differentially expressed microRNAs after TARBP2 overexpression. ..

    Software:

    Article Title: Pre-processing and differential expression analysis of Agilent microRNA arrays using the AgiMicroRna Bioconductor library
    Article Snippet: .. Pradervand et al. [ ] carried out a similar investigation using the Agilent microRNA microarray platform and the summarized TGS obtained with the AFE image analysis software provided by the vendor. ..



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    Validation of candidate <t>miRNAs.</t> Among the top rated nine miRNAs screened from our miRNA <t>microarray,</t> four miRNAs involving (A) hsa-miR-145-5p, (B) hsa-miR-497-5p, (C) hsa-miR-29a-3p and (D) hsa-miR-204-5p were also significantly altered in GSE40355. miRNA, microRNA.
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    Image Search Results


    Flowchart of microarray data analysis. Swine monocytes were exposed to Bb12 with or without the addition of a blocking antibody anti-TLR2. Groups were as follows: unstimulated swine monocytes, monocytes stimulated with Bb12 for 4 h, and swine monocytes incubated with anti-TLR2 antibody and Bb12 for 4 h. Microarray was performed, and 40 microRNAs with a MFI > 500 were selected for analysis of molecular interactions (KEGG analysis). The microRNAs were also analyzed for miRNA–mRNA interactions within TLR2 pathway targets (miRTarBase). After this, 15 miRNAs with a reported interaction with TLR2 pathway–related target proteins were selected to analyze with a multiple t test

    Journal: Probiotics and Antimicrobial Proteins

    Article Title: Immunomodulation by Bifidobacterium animalis subsp. lactis Bb12: Integrative Analysis of miRNA Expression and TLR2 Pathway–Related Target Proteins in Swine Monocytes

    doi: 10.1007/s12602-021-09816-1

    Figure Lengend Snippet: Flowchart of microarray data analysis. Swine monocytes were exposed to Bb12 with or without the addition of a blocking antibody anti-TLR2. Groups were as follows: unstimulated swine monocytes, monocytes stimulated with Bb12 for 4 h, and swine monocytes incubated with anti-TLR2 antibody and Bb12 for 4 h. Microarray was performed, and 40 microRNAs with a MFI > 500 were selected for analysis of molecular interactions (KEGG analysis). The microRNAs were also analyzed for miRNA–mRNA interactions within TLR2 pathway targets (miRTarBase). After this, 15 miRNAs with a reported interaction with TLR2 pathway–related target proteins were selected to analyze with a multiple t test

    Article Snippet: A total of 2 μg RNA from each sample was sent for genome-wide microRNA microarray analysis using μParaflo® microfluidic biochip technology; this service was provided by LC Sciences (Houston, TX, USA).

    Techniques: Microarray, Blocking Assay, Incubation

    Comparison of qRT-PCR and microarray results. Log2 fold change expression between unstimulated monocytes and Bb12-stimulated cells by qRT-PCR and microarray

    Journal: Probiotics and Antimicrobial Proteins

    Article Title: Immunomodulation by Bifidobacterium animalis subsp. lactis Bb12: Integrative Analysis of miRNA Expression and TLR2 Pathway–Related Target Proteins in Swine Monocytes

    doi: 10.1007/s12602-021-09816-1

    Figure Lengend Snippet: Comparison of qRT-PCR and microarray results. Log2 fold change expression between unstimulated monocytes and Bb12-stimulated cells by qRT-PCR and microarray

    Article Snippet: A total of 2 μg RNA from each sample was sent for genome-wide microRNA microarray analysis using μParaflo® microfluidic biochip technology; this service was provided by LC Sciences (Houston, TX, USA).

    Techniques: Comparison, Quantitative RT-PCR, Microarray, Expressing

    Mir-92b promoted osteogenesis in MSCs (A–B) The top three up/down-regulated microRNAs in De-Os-MSCs were listed, and verified by qPCR (B) (C–E) The scrambled control, let-7e, mir-10b, mir-20a, mir-92b, mir-371 and mir-373 were transduced into MSCs with lentiviruses. The overexpression of each microRNA was verified by qPCR (C). The infected MSCs were induced to undergo osteogenic differentiation for 10 days, then the calcium deposits were stained with Alizarin Red S (D), and quantified (E) (F) Total RNA was extracted from MSCs infected with mir-92b or scrambled control. The mRNA expression levels of Osterix, Runx2, OPN and ALP were detected by qPCR. β-actin was used as an internal control. The data was expressed as mean ​± ​SD (n ​= ​3). ∗p ​< ​0.05 (G–I) Total proteins were extracted from MSCs transduced with scrambled control or mir-92b. Then the proteins were analyzed by western blot using indicated antibodies. The protein levels of pERK (H) and pJNK (I) was normalized to ERK and JNK1 respectively. All the data represent mean ​± ​SD of three independent experiments. ∗p ​< ​0.05 (J–K) The mir-92b antagmir was transfected into MSCs, then the cells were treated with osteogenic induction medium for 10 days, the calcium deposits were stained with Alizarin Red S (J), the changes of osteogenesis-related genes was checked by qPCR (K).

    Journal: Journal of Orthopaedic Translation

    Article Title: De-osteogenic-differentiated mesenchymal stem cells accelerate fracture healing by mir-92b

    doi: 10.1016/j.jot.2020.10.009

    Figure Lengend Snippet: Mir-92b promoted osteogenesis in MSCs (A–B) The top three up/down-regulated microRNAs in De-Os-MSCs were listed, and verified by qPCR (B) (C–E) The scrambled control, let-7e, mir-10b, mir-20a, mir-92b, mir-371 and mir-373 were transduced into MSCs with lentiviruses. The overexpression of each microRNA was verified by qPCR (C). The infected MSCs were induced to undergo osteogenic differentiation for 10 days, then the calcium deposits were stained with Alizarin Red S (D), and quantified (E) (F) Total RNA was extracted from MSCs infected with mir-92b or scrambled control. The mRNA expression levels of Osterix, Runx2, OPN and ALP were detected by qPCR. β-actin was used as an internal control. The data was expressed as mean ​± ​SD (n ​= ​3). ∗p ​< ​0.05 (G–I) Total proteins were extracted from MSCs transduced with scrambled control or mir-92b. Then the proteins were analyzed by western blot using indicated antibodies. The protein levels of pERK (H) and pJNK (I) was normalized to ERK and JNK1 respectively. All the data represent mean ​± ​SD of three independent experiments. ∗p ​< ​0.05 (J–K) The mir-92b antagmir was transfected into MSCs, then the cells were treated with osteogenic induction medium for 10 days, the calcium deposits were stained with Alizarin Red S (J), the changes of osteogenesis-related genes was checked by qPCR (K).

    Article Snippet: The microRNA microarray analysis was performed by the Annoroad Gene Technology Corporation (Beijing, China).

    Techniques: Control, Over Expression, Infection, Staining, Expressing, Transduction, Western Blot, Transfection

    Validation of candidate miRNAs. Among the top rated nine miRNAs screened from our miRNA microarray, four miRNAs involving (A) hsa-miR-145-5p, (B) hsa-miR-497-5p, (C) hsa-miR-29a-3p and (D) hsa-miR-204-5p were also significantly altered in GSE40355. miRNA, microRNA.

    Journal: Molecular Medicine Reports

    Article Title: Identification and bioinformatics analysis of miRNAs associated with human muscle invasive bladder cancer

    doi: 10.3892/mmr.2017.7726

    Figure Lengend Snippet: Validation of candidate miRNAs. Among the top rated nine miRNAs screened from our miRNA microarray, four miRNAs involving (A) hsa-miR-145-5p, (B) hsa-miR-497-5p, (C) hsa-miR-29a-3p and (D) hsa-miR-204-5p were also significantly altered in GSE40355. miRNA, microRNA.

    Article Snippet: After assessing RNA quality and quantity, the miRNAs microarray analysis (Affymetrix microRNA 4.0 Array, Affymetrix, Inc., Santa Clara, CA, USA) was performed according to the manufacturer's instructions.

    Techniques: Microarray