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Methylflash global dna methylation 5 mc elisa easy kit

Manufactured by Epigentek
Sourced in United States

The MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit is a laboratory equipment product designed to quantify the global DNA methylation levels in a given sample. The kit utilizes an enzyme-linked immunosorbent assay (ELISA) technique to detect and measure the presence of 5-methylcytosine (5-mC) in DNA samples.

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44 protocols using methylflash global dna methylation 5 mc elisa easy kit

1

Global DNA Methylation Quantification

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For the percentage of 5-methylcytosine in global DNA methylation in AGS cells, a MethylFlash Global DNA methylation (5-mc) ELISA Easy Kit (Epigentek) was used. Briefly, DNA samples (100 ng) were bound to high DNA affinity strip wells. Methylated DNA was detected using the capture and detection antibodies to 5-methyl cytosine, and then quantified colorimetrical by reading the absorbance at 450 nm using a model 680 microplate reader. The amount of methylated DNA was proportional to the optical density (OD) intensity measured. The absolute amount of methylated DNA was quantified as per protocol using a standard curve, plotting the OD values vs. 5 serial dilution of control methylated DNA (0.5−10 ng).
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2

Quantifying Global DNA Methylation

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Genomic DNA was isolated from hepatopancreas samples using the GenElute™ Mammalian Genomic DNA Miniprep Kit (Merck KGaA, Darmstadt, Germany) according to the manufacturer’s directions. The DNA purity was checked by UV absorption (260/280 nm, DS-11 Spectrophotometer, DeNovix, Wilmington, NC, USA) [7 (link)]. Total 5mC DNA level was quantified using the MethylFlash Global DNA Methylation (5mC) ELISA Easy Kit (EpiGentek, Farmingdale, NY, USA). This kit provides a fast and precise method to determine global DNA methylation changes, with a detection limit of 5 nanograms (ng) of fully methylated DNA. In addition, the use of such ELISA-based assays for serial measurements of 5mC can serve as a cost-effective and reliable alternative to commonly used methods for whole-genome DNA methylation quantitation, such as chromatography, radioactive filter-binding, or bisulfite sequencing-based methods [32 (link),33 (link)]. Optical density (OD) was measured at a wavelength of 450 nanometers (nm) with a Stat Fax 4200 microplate reader (Awareness Technology, Palm City, FL, USA). For absolute 5mC quantifications, a standard curve was created by graphing the corresponding ODs versus the log10-transformed concentrations of the positive controls. The coefficients of determination (R2) for ELISA calibration curves were above 0.97; an example is shown in Figure 1.
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3

Quantifying Global DNA Methylation

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The 5-methylcytosine level in the DNA of LPLs was measured using a MethylFlash Global DNA
Methylation (5-mC) ELISA Easy Kit (Epigentek Group Inc., Farmingdale, NY, USA) according
to the manufacturer’s protocol. The absorbance of each well at 450 nm was measured using a
Varioskan Flash microplate reader (Thermo Fisher Scientific, Waltham, MA, USA), and the
5-mC concentration was calculated using a standard curve.
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4

Quantifying Global DNA Methylation

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Genomic DNA was extracted from hepatopancreas and ovotestis with the GenElute™ Mammalian Genomic DNA Miniprep Kit (Merck KGaA, Darmstadt, Germany) as per manufacturer’s instructions. A DS-11 Spectrophotometer (DeNovix, Wilmington, USA) was used to evaluate DNA purity by determining a sample absorbance spectrum at 260 nm and 280 nm, and calculating the A260/A280 ratio. Genome-wide 5mC levels in DNA samples were assessed using the MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (EpiGentek, East Farmingdale, NY, USA), as previously described (Georgescu et al., 2021 (link)). Optical density (OD) was measured at 450 nanometers using a Stat Fax 4200 microplate reader (Awareness Technology, Palm City, FL, USA). For absolute 5-mC quantification, a standard curve was obtained by plotting the various concentrations of the positive controls against the corresponding ODs.
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5

Quantification of Epigenetic and Metabolic Markers

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Total level of 5-mC and 5-hmC in genomic DNA was determined using MethylFlash Global DNA methylation (5-mC) ELISA Easy Kit (P-1030, EpiGentek) and Global 5-hmC Quantification kit (55018, Active Motif), respectively. Cellular content of αKG was determined by alpha KG Assay Kit (ab83431, abeam). Serum levels of SOD3 was determined using an ELISA, for mouse serum (OKCD01107, Aviva System Biology), for human serum (MBS2701262, MyBioSource). TET1 activity was analyzed by Epigenase 5mC-Hydroxylase TET Activity/Inhibition Assay Kit (P-3086, EpiGentek). Plasma insulin were measured using Ultra Sensitive Mouse Insulin ELISA kits (90080, Crystal Chem Inc.). Plasma 25(OH) vitamin D were measured using total 25-OH Vitamin D IVD ELISA kit (RDKAP1971, R&D systems). All assays were performed according to the manufacturer’s protocols.
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6

Epigenetic Regulation Analysis Protocol

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The total DNA of cell samples was isolated using the Ezup Column Animal Genomic DNA Purification Kit (Sangon Biotech, shanghai, China) for the DNA methylation analysis. The purity and concentration of DNA were measured by a spectrophotometer (Implen, Munich, Germany). The total DNA methylation levels were analyzed using the MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (Epigentek Group Inc., Farmingdale, NY, USA). Nuclear protein was isolated using the Nucleoprotein Extraction Kit (Sangon Biotech, Shanghai, China) for histone acetylation and HAT and HDAC activity analyses. The concentration of nuclear protein was measured using the BCA Protein Assay Kit (Sangon Biotech, Shanghai, China) and a microplate reader (Thermo Fisher Scientific, Waltham, MA, USA). The acetylation levels of histone H3 and H4 were analyzed by Western Blot. The activity of DNMT, HAT, and HDAC was detected by the EpiQuik™ DNMT Activity/Inhibition Assay Ultra Kit (Epigentek Group Inc., Farmingdale, NY, USA), HAT Activity Colorimetric Assay Kit (BioVision, Milpitas, CA, USA), and HDAC Activity Colorimetric Assay Kit (BioVision, Milpitas, CA, USA), respectively. All assays were performed according to the manufacturer’s instructions.
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7

Quantifying Global DNA Methylation

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Two hundred nanograms of genome DNA were harvested, and DNA methylation levels were detected by MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (p-1030, EpiGentek) according to the manufacturer’s instructions. All experiments were conducted three times in triplicate. Results are shown as mean ± SEM.
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8

Quantifying DNA Methylation in Fibroblasts

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Fibroblasts plated on glass or PAAm gels of varying stiffness for 2 days were trypsinized, and DNA was extracted by using the Invitrogen PureLink Genomic DNA Mini Kit (Invitrogen, K1820-01). The 5-mC level was analyzed by using the MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (Epigentek, P-1030) according to the manufacturer’s instructions. Briefly, 100 ng of sample DNA was bonded into the assay wells and incubated with a 5-mC detection complex solution for 60 min. Then, color developer solution was added into assay wells, and the absorbance at 450 nm was measured using a plate reader (Infinite 200Pro, 30050303).
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9

Global DNA Methylation Analysis by ELISA

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Global DNA methylation was evaluated through the MethylFlash™ Global DNA Methylation (5-mC) ELISA Easy Kit (EpiGentek Group Inc, NY, United States) measuring levels of 5-methylcytosine (5-mC). About 100 ng of input DNA from GBM cells, extracted using the previously described protocol, was added to a microplate well with a high affinity for DNA binding. Negative control (NC) and different percentages of positive control (PC) were prepared according to the manufacturer’s indications to set the standard curve and determine the slope. The plate was covered and incubated at 37°C for 60 min. Following washing, 5-mC detection complex solution was added to the plate and removed after 50 min at room temperature. Colorimetric reaction was triggered by the addition of Developer Solution and stopped when the 5% PC turned medium blue. Absorbance was immediately read at 450 nm. DNA methylation was calculated as follows: 5mC%=SampleODNCODSlope×inputDNAamount(ng)×100.
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10

DNA Extraction and Methylation Quantification

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Genomic DNA of the cells was extracted using the TIANamp Genomic DNA Kit (TIANGEN, Beijing, China). DNA methylation was measured using the colorimetric MethylFlash Global DNA Methylation 5-mC ELISA Easy Kit (Epigentek, Farmingdale, NY, United States) according to the manufacturer’s instructions.
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