control genomic dna Search Results


control genomic dna porcine female  (AMS Biotechnology)
86
AMS Biotechnology control genomic dna porcine female
Control Genomic Dna Porcine Female, supplied by AMS Biotechnology, 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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Average 86 stars, based on 1 article reviews
control genomic dna porcine female - by Bioz Stars, 2026-04
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control genomic dna  (Coriell Institute for Medical Research)
90
Coriell Institute for Medical Research control genomic dna
Control Genomic Dna, supplied by Coriell Institute for Medical Research, 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/control genomic dna/product/Coriell Institute for Medical Research
Average 90 stars, based on 1 article reviews
control genomic dna - by Bioz Stars, 2026-04
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control genomic dna from male rabbit  (Zyagen Inc)
90
Zyagen Inc control genomic dna from male rabbit
Control Genomic Dna From Male Rabbit, supplied by Zyagen 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/control genomic dna from male rabbit/product/Zyagen Inc
Average 90 stars, based on 1 article reviews
control genomic dna from male rabbit - by Bioz Stars, 2026-04
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completely methylated unmethylated control genomic dna  (Qiagen)
90
Qiagen completely methylated unmethylated control genomic dna
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Completely Methylated Unmethylated Control Genomic Dna, supplied by Qiagen, 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/completely methylated unmethylated control genomic dna/product/Qiagen
Average 90 stars, based on 1 article reviews
completely methylated unmethylated control genomic dna - by Bioz Stars, 2026-04
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genomic dna contamination control (pa-031)  (Qiagen)
90
Qiagen genomic dna contamination control (pa-031)
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Genomic Dna Contamination Control (Pa 031), supplied by Qiagen, 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/genomic dna contamination control (pa-031)/product/Qiagen
Average 90 stars, based on 1 article reviews
genomic dna contamination control (pa-031) - by Bioz Stars, 2026-04
90/100 stars
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control human dna  (Promega)
90
Promega control human dna
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Control Human Dna, supplied by Promega, 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/control human dna/product/Promega
Average 90 stars, based on 1 article reviews
control human dna - by Bioz Stars, 2026-04
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isolated dna from gm maize events nk603  (Fluka Chemical)
90
Fluka Chemical isolated dna from gm maize events nk603
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Isolated Dna From Gm Maize Events Nk603, supplied by Fluka Chemical, 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/isolated dna from gm maize events nk603/product/Fluka Chemical
Average 90 stars, based on 1 article reviews
isolated dna from gm maize events nk603 - by Bioz Stars, 2026-04
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t-cell genomic dna supplied by the manufacturer as positive control  (Adaptive Biotechnologies Corp)
90
Adaptive Biotechnologies Corp t-cell genomic dna supplied by the manufacturer as positive control
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
T Cell Genomic Dna Supplied By The Manufacturer As Positive Control, supplied by Adaptive Biotechnologies Corp, 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/t-cell genomic dna supplied by the manufacturer as positive control/product/Adaptive Biotechnologies Corp
Average 90 stars, based on 1 article reviews
t-cell genomic dna supplied by the manufacturer as positive control - by Bioz Stars, 2026-04
90/100 stars
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human genomic tonsil dna igh neg control  (Invivoscribe Inc)
90
Invivoscribe Inc human genomic tonsil dna igh neg control
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Human Genomic Tonsil Dna Igh Neg Control, supplied by Invivoscribe 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/human genomic tonsil dna igh neg control/product/Invivoscribe Inc
Average 90 stars, based on 1 article reviews
human genomic tonsil dna igh neg control - by Bioz Stars, 2026-04
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control genomic dna  (Promega)
90
Promega control genomic dna
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Control Genomic Dna, supplied by Promega, 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/control genomic dna/product/Promega
Average 90 stars, based on 1 article reviews
control genomic dna - by Bioz Stars, 2026-04
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tumor genomic dna or non-tumor control tissue  (Illumina Inc)
90
Illumina Inc tumor genomic dna or non-tumor control tissue
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Tumor Genomic Dna Or Non Tumor Control Tissue, supplied by Illumina 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/tumor genomic dna or non-tumor control tissue/product/Illumina Inc
Average 90 stars, based on 1 article reviews
tumor genomic dna or non-tumor control tissue - by Bioz Stars, 2026-04
90/100 stars
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rat genomic dna negative control primer set  (Qiagen)
90
Qiagen rat genomic dna negative control primer set
Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that <t>were</t> <t>methylated</t> (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated <t>DNA.</t> C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.
Rat Genomic Dna Negative Control Primer Set, supplied by Qiagen, 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/rat genomic dna negative control primer set/product/Qiagen
Average 90 stars, based on 1 article reviews
rat genomic dna negative control primer set - by Bioz Stars, 2026-04
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Image Search Results


Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that were methylated (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated DNA. C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.

Journal: The Journal of Biological Chemistry

Article Title: Epithelial Cell Adhesion Molecule Regulation Is Associated with the Maintenance of the Undifferentiated Phenotype of Human Embryonic Stem Cells *

doi: 10.1074/jbc.M109.077081

Figure Lengend Snippet: Methylation status of EpCAM promoter regions in undifferentiated and differentiated hESCs. A, schematic representation of the EpCAM gene promoter region. Primers for MSP and bisulfite sequencing used in the study are indicated. B, MSP analysis of the EpCAM gene promoter region in undifferentiated and differentiated H9 cells. The PCR products that were methylated (M) were generated by methylation-specific primers, and those that were unmethylated (U) were generated by primers specific for unmethylated DNA. C, mapping the methylation status of the CpG islands in the promoter region of the EpCAM gene by bisulfite sequencing. Each row of squares represents a single plasmid cloned and sequenced from PCR products generated from amplification of bisulfite-treated DNA. Open squares, unmethylated cytosines; filled squares, methylated cytosines. Most CpGs in the promoter region in both undifferentiated and differentiated H9 cells were unmethylated.

Article Snippet: Completely methylated and unmethylated control genomic DNA was purchased from Qiagen (Qiagen Inc., Valencia, CA).

Techniques: Methylation, Methylation Sequencing, Generated, Plasmid Preparation, Clone Assay, Amplification