massarray methylation analysis Search Results


90
CapitalBio Corporation massarray methylation profiling and data analysis
Massarray Methylation Profiling And Data Analysis, supplied by CapitalBio Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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, 2026-05
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86
Sequenom sequenom massarray methylation
Fig. 4. Cd interfered with the DNA <t>methylation</t> of Oct4 and Nanog of mouse ES cells into ovarian GCs. A and E represented the methylation status of CpG islands on DNA templates in the promoter regions of both factors was evaluated using the Sequenom <t>MassARRAY</t> Methylation. B and F: DNA methylation rate of CpG locus in the promoter region of different sites of both factors. C–K represented the degree of DNA methylation on different fragments of the factors in maps and DNA methylation rate in the promoter region in each fragment and groups. Data are presented as the mean ± SD, *P < 0.05 compared with the IA group.
Sequenom Massarray Methylation, supplied by Sequenom, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


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

Fig. 4. Cd interfered with the DNA methylation of Oct4 and Nanog of mouse ES cells into ovarian GCs. A and E represented the methylation status of CpG islands on DNA templates in the promoter regions of both factors was evaluated using the Sequenom MassARRAY Methylation. B and F: DNA methylation rate of CpG locus in the promoter region of different sites of both factors. C–K represented the degree of DNA methylation on different fragments of the factors in maps and DNA methylation rate in the promoter region in each fragment and groups. Data are presented as the mean ± SD, *P < 0.05 compared with the IA group.

Journal: Multiple sclerosis and related disorders

Article Title: Ultra-high field spinal cord MRI in multiple sclerosis: Where are we standing? A literature review.

doi: 10.1016/j.msard.2021.103436

Figure Lengend Snippet: Fig. 4. Cd interfered with the DNA methylation of Oct4 and Nanog of mouse ES cells into ovarian GCs. A and E represented the methylation status of CpG islands on DNA templates in the promoter regions of both factors was evaluated using the Sequenom MassARRAY Methylation. B and F: DNA methylation rate of CpG locus in the promoter region of different sites of both factors. C–K represented the degree of DNA methylation on different fragments of the factors in maps and DNA methylation rate in the promoter region in each fragment and groups. Data are presented as the mean ± SD, *P < 0.05 compared with the IA group.

Article Snippet: The DNA methylation levels of the upstream promoter regions of the four markers were detected by the Sequenom MassARRAY Methylation method combined with the dedicated analysis software MethPrimer.

Techniques: DNA Methylation Assay, Methylation

Fig. 5. Cd interfered with the DNA methylation of Amhr2 and Sox2 of mouse ES cells into ovarian GCs. A and E represented the methylation status of CpG islands on DNA templates in the promoter regions of both factors was evaluated using the Sequenom MassARRAY Methylation. B and F: DNA methylation rate of CpG locus in the promoter region of different sites of both factors. C-K represented the degree of DNA methylation on different fragments of the factors in maps and DNA methylation rate in the promoter region in each fragment and groups. Data are presented as the mean ± SD, *P < 0.05 compared with the IA group.

Journal: Multiple sclerosis and related disorders

Article Title: Ultra-high field spinal cord MRI in multiple sclerosis: Where are we standing? A literature review.

doi: 10.1016/j.msard.2021.103436

Figure Lengend Snippet: Fig. 5. Cd interfered with the DNA methylation of Amhr2 and Sox2 of mouse ES cells into ovarian GCs. A and E represented the methylation status of CpG islands on DNA templates in the promoter regions of both factors was evaluated using the Sequenom MassARRAY Methylation. B and F: DNA methylation rate of CpG locus in the promoter region of different sites of both factors. C-K represented the degree of DNA methylation on different fragments of the factors in maps and DNA methylation rate in the promoter region in each fragment and groups. Data are presented as the mean ± SD, *P < 0.05 compared with the IA group.

Article Snippet: The DNA methylation levels of the upstream promoter regions of the four markers were detected by the Sequenom MassARRAY Methylation method combined with the dedicated analysis software MethPrimer.

Techniques: DNA Methylation Assay, Methylation