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mass-spectrometry based sequenom massarray epityper platform  (Sequenom)

 
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    Sequenom mass-spectrometry based sequenom massarray epityper platform
    TABLE IV
    Mass Spectrometry Based Sequenom Massarray Epityper Platform, supplied by Sequenom, 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/mass-spectrometry+based+sequenom+massarray+epityper+platform/sequenom+epityper/pmc03999958-90-89-91
    Average 90 stars, based on 1 article reviews
    mass-spectrometry based sequenom massarray epityper platform - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver"

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver

    Journal: Environmental and molecular mutagenesis

    doi: 10.1002/em.21823

    TABLE IV
    Figure Legend Snippet: TABLE IV

    Techniques Used: DNA Methylation Assay

    Related Articles

    DNA Methylation Assay:

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver
    Article Snippet: A standard HotStarTaq thermal cycling setting was used for the three assays with the following changes: CES2 required annealing at 56°C for 30 sec at 35 cycles, COMT required annealing at 60°C for 30 sec at 35 cycles, and SULT2A1 required annealing at 56°C for 30 sec at 40 cycles. table ft1 table-wrap mode=article t1 TABLE IV caption a4 Sequenom Epityper Primer Assays for DNA Methylation After in vitro transcription and uracil-cleavage of amplicons as previously described [ Coolen et al., 2007 ], promoter methylation was quantified using the mass-spectrometry based Sequenom MassArray EpiTYPER platform (Sequenom, San Diego, CA) in the University of Michigan DNA Sequencing Core.

    In Vitro:

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver
    Article Snippet: A standard HotStarTaq thermal cycling setting was used for the three assays with the following changes: CES2 required annealing at 56°C for 30 sec at 35 cycles, COMT required annealing at 60°C for 30 sec at 35 cycles, and SULT2A1 required annealing at 56°C for 30 sec at 40 cycles. table ft1 table-wrap mode=article t1 TABLE IV caption a4 Sequenom Epityper Primer Assays for DNA Methylation After in vitro transcription and uracil-cleavage of amplicons as previously described [ Coolen et al., 2007 ], promoter methylation was quantified using the mass-spectrometry based Sequenom MassArray EpiTYPER platform (Sequenom, San Diego, CA) in the University of Michigan DNA Sequencing Core.

    Methylation:

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver
    Article Snippet: A standard HotStarTaq thermal cycling setting was used for the three assays with the following changes: CES2 required annealing at 56°C for 30 sec at 35 cycles, COMT required annealing at 60°C for 30 sec at 35 cycles, and SULT2A1 required annealing at 56°C for 30 sec at 40 cycles. table ft1 table-wrap mode=article t1 TABLE IV caption a4 Sequenom Epityper Primer Assays for DNA Methylation After in vitro transcription and uracil-cleavage of amplicons as previously described [ Coolen et al., 2007 ], promoter methylation was quantified using the mass-spectrometry based Sequenom MassArray EpiTYPER platform (Sequenom, San Diego, CA) in the University of Michigan DNA Sequencing Core.

    DNA Sequencing:

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver
    Article Snippet: A standard HotStarTaq thermal cycling setting was used for the three assays with the following changes: CES2 required annealing at 56°C for 30 sec at 35 cycles, COMT required annealing at 60°C for 30 sec at 35 cycles, and SULT2A1 required annealing at 56°C for 30 sec at 40 cycles. table ft1 table-wrap mode=article t1 TABLE IV caption a4 Sequenom Epityper Primer Assays for DNA Methylation After in vitro transcription and uracil-cleavage of amplicons as previously described [ Coolen et al., 2007 ], promoter methylation was quantified using the mass-spectrometry based Sequenom MassArray EpiTYPER platform (Sequenom, San Diego, CA) in the University of Michigan DNA Sequencing Core.



    Similar Products

    mass-spectrometry based sequenom massarray epityper platform  (Sequenom)
    90
    Sequenom mass-spectrometry based sequenom massarray epityper platform
    TABLE IV
    Mass Spectrometry Based Sequenom Massarray Epityper Platform, supplied by Sequenom, 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/mass-spectrometry+based+sequenom+massarray+epityper+platform/sequenom+epityper/pmc03999958-90-89-91
    Average 90 stars, based on 1 article reviews
    mass-spectrometry based sequenom massarray epityper platform - by Bioz Stars, 2026-09
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    TABLE IV

    Journal: Environmental and molecular mutagenesis

    Article Title: Bisphenol A-Associated Alterations in the Expression and Epigenetic Regulation of Genes Encoding Xenobiotic Metabolizing Enzymes in Human Fetal Liver

    doi: 10.1002/em.21823

    Figure Lengend Snippet: TABLE IV

    Article Snippet: A standard HotStarTaq thermal cycling setting was used for the three assays with the following changes: CES2 required annealing at 56°C for 30 sec at 35 cycles, COMT required annealing at 60°C for 30 sec at 35 cycles, and SULT2A1 required annealing at 56°C for 30 sec at 40 cycles. table ft1 table-wrap mode=article t1 TABLE IV caption a4 Sequenom Epityper Primer Assays for DNA Methylation After in vitro transcription and uracil-cleavage of amplicons as previously described [ Coolen et al., 2007 ], promoter methylation was quantified using the mass-spectrometry based Sequenom MassArray EpiTYPER platform (Sequenom, San Diego, CA) in the University of Michigan DNA Sequencing Core.

    Techniques: DNA Methylation Assay