Methylamp Whole Cell Bisulfite Modification Kit
Product Description
- Proprietary and unique by directly modifying cells and tissues
- Suitable for minute amounts of starting material, e.g. microdissection samples
- Rapid streamlined 3 hour procedure from cells/tissues to modified DNA
- Completely converts unmethylated cytosine into uracil: modified DNA > 99.5%
- The lowest degradation of DNA in the modification process: more than 90% of DNA loss can be prevented with a unique DNA protection buffer
The Methylamp Whole Cell Bisulfite Modification Kit is an innovative and unique set of essential components which enables the analysis of DNA methylation and DNA modification directly from cells or tissues using Epigentek's uniquely simplified and streamlined bisulfite method. The entire procedure can be completed within only 3 hours. The Methylamp Whole Cell Bisulfite Modification Kit is specifically designed for DNA methylation research using minute amounts of starting materials including cells cultured in 96-well/384 well plates, tissue section samples, microdissection samples, tissue biopsy and early embryonic cells/oocytes.
Eluted modified DNA by using the Methylamp Whole Cell Bisulfite Modification Kit is suited for real time MS-PCR. It is also suitable for all techniques currently used for the analysis of DNA methylation; including conventional MS-PCR, bisulfite sequencing, pyrosequencing, and methylation microarray. If you use the Methylamp™ Whole Cell Bisulfite Modification Kit for MSP, the numbers of PCR cycles should be greater than 45. The amount of starting materials for each modification can be 100-20000 cells, or 1 µg-100 µg tissues, or 0.2-2 mm2 tissue section samples. For optimal modification, the amount should be 500- 5000 cells, or 5-20 µg tissues, or 0.5-1 mm2 tissue section samples, respectively.
Procedure
The Methylamp Whole Cell Bisulfite Modification Kit contains all reagents required for bisulfite conversion directly on a cell or tissue sample. The kit allows DNA to be isolated from cells or tissues, denatured and bisulfite modified simultaneously in same tube with the specific reaction buffer under the thermodynamic condition. In the modification process, bisulfite reagent reacts specifically with single-stranded DNA, thereby deaminating cytosine and creating a uracil residue. The unique DNA protection reagents contained in the modification buffer can prevent the chemical and thermophilic degradation of DNA in the bisulfite treatment. The non-toxic modified DNA capture buffer enables DNA to tightly bind to the column filter, thus DNA cleaning can be carried out on the column to effectively remove residual sodium bisulfite and salts.
Performance Data
Analysis of DNA methylation from small sample amounts.
Product Citations
- Asano K. et. al. (2021) Combination Chemoradiotherapy with Temozolomide, Vincristine, and Interferon-β Might Improve Outcomes Regardless of O6-Methyl-Guanine-DNA-Methyltransferase (MGMT) Promoter Methylation Status in Newly Glioblastoma BMC Cancer
- Rapado-González Ó, López-Cedrún JL, López-López R, Rodríguez-Ces AM, Suárez-Cunqueiro MM (2021) Saliva Gene Promoter Hypermethylation as a Biomarker in Oral Cancer. J Clin Med
- Todorova K et al. (2017) Micro-RNA-204 Participates in TMPRSS2/ERG Regulation and Androgen Receptor Reprogramming in Prostate Cancer. Horm Cancer
- Serravalle S et al. (2016) Synergistic Cytotoxic Effect of L-Asparaginase Combined with Decitabine as a Demethylating Agent in Pediatric T-ALL, with Specific Epigenetic Signature. Biomed Res Int 2016:1985750
- Ohno R et al. (2013) A replication-dependent passive mechanism modulates DNA demethylation in mouse primordial germ cells. Development 140(14):2892-903
- Catalog Number
P-1016-80-EP - Supplier
EpigenTek - Size
- Shipping
RT