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massarray dna methylation analysis  (SPSS Inc)

 
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    SPSS Inc massarray dna methylation analysis
    The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for <t> Massarray DNA methylation analysis </t>
    Massarray Dna Methylation Analysis, supplied by SPSS Inc, 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/massarray dna methylation analysis/product/SPSS Inc
    Average 90 stars, based on 1 article reviews
    massarray dna methylation analysis - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "HLA-DRB1 and HLA-DQB1 methylation changes promote the occurrence and progression of Kazakh ESCC"

    Article Title: HLA-DRB1 and HLA-DQB1 methylation changes promote the occurrence and progression of Kazakh ESCC

    Journal: Epigenetics

    doi: 10.4161/15592294.2014.969625

    The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for Massarray DNA methylation analysis
    Figure Legend Snippet: The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for Massarray DNA methylation analysis

    Techniques Used: DNA Methylation Assay, Amplification



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    Image Search Results


    ZNF582-AS1 expression was regulated by DNA methylation in ccRCC. a Detection of CpG islands in ZNF582-AS1 promoter and design of MSP primers. The horizontal axis of the curved lines represents the input sequence of ZNF582-AS1, and the vertical axis of the curved lines represents GC percentage. TSS: Transcription Start Sites. b MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC cell lines. c MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC tissues. d Detection of 38 CpG sites in ZNF582-AS1 promoter. e Quantitative detection of DNA methylation level of 38 CpG sites in ZNF582-AS1 promoter using Sequenom MassARRAY quantitative DNA methylation analysis. f and g Comparison of the DNA methylation levels of 38 CpG sites in ccRCC and adjacent normal renal tissues. h Treatment with 5-aza-dC and TSA demethylated ZNF582-AS1 promoter and increased ZNF582-AS1 expression in OSRC2 and Caki-1 cells. T refers to Tumor tissue of ccRCC, N refers to Adjacent normal kidney tissue. M = Methylated, U = Unmethylated

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: Downregulation of lncRNA ZNF582-AS1 due to DNA hypermethylation promotes clear cell renal cell carcinoma growth and metastasis by regulating the N(6)-methyladenosine modification of MT-RNR1

    doi: 10.1186/s13046-021-01889-8

    Figure Lengend Snippet: ZNF582-AS1 expression was regulated by DNA methylation in ccRCC. a Detection of CpG islands in ZNF582-AS1 promoter and design of MSP primers. The horizontal axis of the curved lines represents the input sequence of ZNF582-AS1, and the vertical axis of the curved lines represents GC percentage. TSS: Transcription Start Sites. b MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC cell lines. c MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC tissues. d Detection of 38 CpG sites in ZNF582-AS1 promoter. e Quantitative detection of DNA methylation level of 38 CpG sites in ZNF582-AS1 promoter using Sequenom MassARRAY quantitative DNA methylation analysis. f and g Comparison of the DNA methylation levels of 38 CpG sites in ccRCC and adjacent normal renal tissues. h Treatment with 5-aza-dC and TSA demethylated ZNF582-AS1 promoter and increased ZNF582-AS1 expression in OSRC2 and Caki-1 cells. T refers to Tumor tissue of ccRCC, N refers to Adjacent normal kidney tissue. M = Methylated, U = Unmethylated

    Article Snippet: TSS: Transcription Start Sites. b MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC cell lines. c MSP analysis of ZNF582-AS1 promoter DNA methylation status in ccRCC tissues. d Detection of 38 CpG sites in ZNF582-AS1 promoter. e Quantitative detection of DNA methylation level of 38 CpG sites in ZNF582-AS1 promoter using Sequenom MassARRAY quantitative DNA methylation analysis. f and g Comparison of the DNA methylation levels of 38 CpG sites in ccRCC and adjacent normal renal tissues. h Treatment with 5-aza-dC and TSA demethylated ZNF582-AS1 promoter and increased ZNF582-AS1 expression in OSRC2 and Caki-1 cells.

    Techniques: Expressing, DNA Methylation Assay, Sequencing, Comparison, Methylation

    Summary of main projects in the PANINI network

    Journal: Aging Clinical and Experimental Research

    Article Title: Physical Activity and Nutrition INfluences In ageing (PANINI): consortium mission statement

    doi: 10.1007/s40520-017-0823-7

    Figure Lengend Snippet: Summary of main projects in the PANINI network

    Article Snippet: 10. University of Bologna , Epigenetics of nutrition in ageing , DNA methylation analysis (gene-targeted) by Sequenom ® MassARRAY EpiTYPER platform , NU-AGE samples and new PANINI data , Changes in DNA methylation patterns induced by dietary and physical interventions. Development of a gene-targeted epigenetic clock.

    Techniques: Battery, Activity Assay, Modification, DNA Methylation Assay, Variant Assay

    The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for Massarray DNA methylation analysis

    Journal: Epigenetics

    Article Title: HLA-DRB1 and HLA-DQB1 methylation changes promote the occurrence and progression of Kazakh ESCC

    doi: 10.4161/15592294.2014.969625

    Figure Lengend Snippet: The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for Massarray DNA methylation analysis

    Article Snippet: The primers used to amplify the HLA-DRB1 and DQB1 translational start codon for Massarray DNA methylation analysis Statistical analysis The SPSS version 13.0 software was employed for all statistical analyses.

    Techniques: DNA Methylation Assay, Amplification