non methylated dna controls Search Results


methylated dna  (Zymo Research)
95
Zymo Research methylated dna
Methylated Dna, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human hct116 dko  (Zymo Research)
95
Zymo Research human hct116 dko
Human Hct116 Dko, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human hct116 dko - by Bioz Stars, 2026-07
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e coli genomic dna  (Zymo Research)
93
Zymo Research e coli genomic dna
E Coli Genomic Dna, supplied by Zymo Research, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human methylated non methylated wga dna set  (Zymo Research)
94
Zymo Research human methylated non methylated wga dna set
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Human Methylated Non Methylated Wga Dna Set, supplied by Zymo Research, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
human methylated non methylated wga dna set - by Bioz Stars, 2026-07
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non methylated dna controls  (Zymo Research)
92
Zymo Research non methylated dna controls
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Non Methylated Dna Controls, supplied by Zymo Research, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
non methylated dna controls - by Bioz Stars, 2026-07
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human whole genome amplified nonmethylated dna  (Zymo Research)
95
Zymo Research human whole genome amplified nonmethylated dna
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Human Whole Genome Amplified Nonmethylated Dna, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human whole genome amplified nonmethylated dna - by Bioz Stars, 2026-07
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methylated puc19 dna  (Zymo Research)
93
Zymo Research methylated puc19 dna
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Methylated Puc19 Dna, supplied by Zymo Research, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
methylated puc19 dna - by Bioz Stars, 2026-07
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fully methylated human control dna  (Nordic BioSite)
90
Nordic BioSite fully methylated human control dna
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Fully Methylated Human Control Dna, supplied by Nordic BioSite, 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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Average 90 stars, based on 1 article reviews
fully methylated human control dna - by Bioz Stars, 2026-07
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dna methylation control package  (DIAGENODE DIAGNOSTICS)
90
DIAGENODE DIAGNOSTICS dna methylation control package
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Dna Methylation Control Package, supplied by DIAGENODE DIAGNOSTICS, 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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Average 90 stars, based on 1 article reviews
dna methylation control package - by Bioz Stars, 2026-07
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methylated control human dna 100  (EpiGentek)
90
EpiGentek methylated control human dna 100
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Methylated Control Human Dna 100, supplied by EpiGentek, 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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Average 90 stars, based on 1 article reviews
methylated control human dna 100 - by Bioz Stars, 2026-07
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cpgenome human methylated & non-methylated dna standard sets s8001  (Merck KGaA)
90
Merck KGaA cpgenome human methylated & non-methylated dna standard sets s8001
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Cpgenome Human Methylated & Non Methylated Dna Standard Sets S8001, supplied by Merck KGaA, 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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Average 90 stars, based on 1 article reviews
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methylated dna unmethylated dna control primers  (DIAGENODE DIAGNOSTICS)
90
DIAGENODE DIAGNOSTICS methylated dna unmethylated dna control primers
Demonstration of DIMPLE multiple qPCR primer design for <t>DNA</t> methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted <t>methylated</t> DNA molecules, and is more challenging for traditional PCR primer design algorithms.
Methylated Dna Unmethylated Dna Control Primers, supplied by DIAGENODE DIAGNOSTICS, 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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Average 90 stars, based on 1 article reviews
methylated dna unmethylated dna control primers - by Bioz Stars, 2026-07
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Image Search Results


Demonstration of DIMPLE multiple qPCR primer design for DNA methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted methylated DNA molecules, and is more challenging for traditional PCR primer design algorithms.

Journal: bioRxiv

Article Title: Scaling Multiplex qPCR Primer Design to 1000-plex using the Degenerate Incomplete Multiplex Primer List Extension (DIMPLE) Algorithm

doi: 10.64898/2026.04.17.719221

Figure Lengend Snippet: Demonstration of DIMPLE multiple qPCR primer design for DNA methylation marker detection. (a) Illustration of the products of bisulfite/APOBEC conversion of DNA. For each DNA locus, up to 4 different sets of primers (8 primers) must be designed to maximize sensitivity to the insert sequence. Alternatively, primer specificity can be used to detect specific methylation states of the primer binding regions. (b) Demonstration of 60-plex qPCR amplification of DNA hypomethylation markers. Here, 120 primers were designed to amplify only the + strands of the converted unmethylated DNA molecules, because unmethylated DNA has the lower sequence diversity than converted methylated DNA molecules, and is more challenging for traditional PCR primer design algorithms.

Article Snippet: For methylation assays, the Human Methylated & Non-Methylated (WGA) DNA Set (Zymo Research) served as reference material.

Techniques: DNA Methylation Assay, Marker, Sequencing, Methylation, Binding Assay, Amplification