Diagenode

MagMeDIP-seq Pacakge V2

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目录号
格式
价格
C02010041
10 rxns
$1,880.00

(Coming soon)

Perform MeDIP-seq experiments, i.e. methylated DNA immunoprecipitation followed by next generation sequencing, to obtain region-resolution assessment of DNA methylation using a highly sensitive 5mC-specific antibody. This technology provides a useful, repeatable, and affordable approach for high-resolution methylome research, providing single-base resolution is not necessary. 

MeDIP-seq methods allow you to:

  •     Perform genome-wide DNA methylation mapping
  •     Detect and identify with high sensitivity differentially methylated regions
  •     Get better insight of your epigentics research

Diagenode MagMeDIP-seq package V2 has been specifically developed and optimized to generate DNA libraries during the MagMeDIP assay from the lowest input amounts and secure high-quality NGS data for DNA methylation analysis. Only 10 ng of sheared genomic DNA is required for IP enrichment and library generation, while preserving the efficiency of the enrichment.

The package contains everything you need for your MeDIP-seq experiment, including highly specific antibody, fully validated reagents for library preparation from enriched methylated DNA, and external control DNA.

Features

  • DNA requirement: 10 ng per reaction
  • Robust, easy-to-use protocol with high reproducibility between replicates and repetitive experiments
  • Highly sensitive 5mC specific antibody (clone 33D3)
  • All-in one kit, fully validated for NGS analysis
  • Extrenal control DNA and qPCR primer pairs for quality controls

  • MeDIP-seq validation

    Figure 2. Excellent sequencing quality. Genomic DNA was extracted from human blood samples and sheared to a mean fragment length of 200 bp. MeDIP-seq libraries were prepared from different starting amounts of gDNA using Diagenode's MagMeDIP-seq Package V2 and sequenced in paired-end 50 bp on Illumina NovaSeq instrument generating around 60 million read pairs per sample. Sequencing statistics reveal that all samples performed well, with mean Phred scores above 30 along the entire reads 1 and 2 (data shown for 50 ng gDNA input after trimming).

    Figure 3. Saturation analysis. Clean reads were aligned to the human genome (hg19) using Burrows-Wheeler aligner (BWA) algorithm after which duplicated and unmapped reads were removed resulting in a mapping efficiency >98% for all samples. Quality and validity check of the mapped MeDIP-seq data was performed using MEDIPS R package. Saturation plots show that all sets of reads have sufficient complexity and depth to saturate the coverage profile of the reference genome and that this is reproducible between replicates and repetitive experiments (data shown for 50 ng gDNA input: left panel = replicate a, right panel = replicate b).

  •  文档
    MagMeDIP-seq package v2 MANUAL
    Magnetic Methylated DNA Immunoprecipitation Package for Illumina sequencing
    Download
    DNA Methylation Solutions BROCHURE
    Complete solution for DNA methylation studies! Whether you are experienced or new to th...
    Download
  •  出版物

    How to properly cite this product in your work

    Diagenode strongly recommends using this: MagMeDIP-seq Pacakge V2 (Diagenode Cat# C02010041). Click here to copy to clipboard.

    Using our products in your publication? Let us know!

    Polycystic ovary syndrome is transmitted via a transgenerational epigenetic process
    Mimouni et. al.
    Polycystic ovary syndrome (PCOS) is the most common reproductive and metabolic disorder affecting women of reproductive age. PCOS has a strong heritable component, but its pathogenesis has been unclear. Here, we performed RNA sequencing and genome-wide DNA methylation profiling of ...

    Integrated epigenetic biomarkers in circulating cell-free DNA as a robust classifier for pancreatic cancer.
    Cao F, Wei A, Hu X, He Y, Zhang J, Xia L, Tu K, Yuan J, Guo Z, Liu H, Xie D, Li A
    BACKGROUND: The high lethal rate of pancreatic cancer is partly due to a lack of efficient biomarkers for screening and early diagnosis. We attempted to develop effective and noninvasive methods using 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) markers from circulating cell-free DNA (cfDNA) for the det...

    Detection and discrimination of intracranial tumors using plasma cell-free DNA methylomes.
    Nassiri F, Chakravarthy A, Feng S, Shen SY, Nejad R, Zuccato JA, Voisin MR, Patil V, Horbinski C, Aldape K, Zadeh G, De Carvalho DD
    Definitive diagnosis of intracranial tumors relies on tissue specimens obtained by invasive surgery. Noninvasive diagnostic approaches provide an opportunity to avoid surgery and mitigate unnecessary risk to patients. In the present study, we show that DNA-methylation profiles from plasma reveal highly specific sign...

    Detection of renal cell carcinoma using plasma and urine cell-free DNA methylomes.
    Nuzzo PV, Berchuck JE, Korthauer K, Spisak S, Nassar AH, Abou Alaiwi S, Chakravarthy A, Shen SY, Bakouny Z, Boccardo F, Steinharter J, Bouchard G, Curran CR, Pan W, Baca SC, Seo JH, Lee GM, Michaelson MD, Chang SL, Waikar SS, Sonpavde G, Irizarry RA, Pome
    Improving early cancer detection has the potential to substantially reduce cancer-related mortality. Cell-free methylated DNA immunoprecipitation and high-throughput sequencing (cfMeDIP-seq) is a highly sensitive assay capable of detecting early-stage tumors. We report accurate classification of patients across all ...

    Preparation of cfMeDIP-seq libraries for methylome profiling of plasma cell-free DNA.
    Shen SY, Burgener JM, Bratman SV, De Carvalho DD
    Circulating cell-free DNA (cfDNA) comprises small DNA fragments derived from normal and tumor tissue that are released into the bloodstream. Recently, methylation profiling of cfDNA as a liquid biopsy tool has been gaining prominence due to the presence of tissue-specific markers in cfDNA. We have previously reporte...

    DNA methylation of the Tacr2 gene in a CUMS model of depression.
    Xiang D, Xiao J, Fu L, Yao L, Wan Q, Xiao L, Zhu F, Wang G, Liu Z
    Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional pr...

    Sensitive tumour detection and classification using plasma cell-free DNA methylomes.
    Shen SY, Singhania R, Fehringer G, Chakravarthy A, Roehrl MHA, Chadwick D, Zuzarte PC, Borgida A, Wang TT, Li T, Kis O, Zhao Z, Spreafico A, Medina TDS, Wang Y, Roulois D, Ettayebi I, Chen Z, Chow S, Murphy T, Arruda A, O'Kane GM, Liu J, Mansour M, McPher
    The use of liquid biopsies for cancer detection and management is rapidly gaining prominence. Current methods for the detection of circulating tumour DNA involve sequencing somatic mutations using cell-free DNA, but the sensitivity of these methods may be low among patients with early-stage cancer given the limited ...

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