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S7847 Sigma-AldrichCpGenome Turbo Bisulfite Modification Kit

The CpGenome Turbo Bisulfite Modification Kit is designed to simplify & streamline the bisulfite modification process. In just 90 minutes go from DNA sample to bisulfite converted DNA ready for analysis.

CpGenome Turbo Bisulfite Modification Kit MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

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S7847

50 reactions

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Description
Catalogue Number	S7847
Trade Name	CpGenome Chemicon
Description	CpGenome Turbo Bisulfite Modification Kit
Overview	The CpGenome Turbo Bisulfite Modification Kit is designed to simplify and streamline the bisulfite modification process. This kit contains all key reagents for bisulfite modification to allow for the recovery of modified DNA in about 90 minutes as compared to 3-16 hours for similar kits. This rapid, but effective approach employs a proprietary mixture of modification reagents to permit shorter conversion times. This unique mixture of reagents allows for complete conversion of unmethylated cytosines while minimizing damage to the input DNA. After modification, and desulfonation, the modifed DNA is purified and eluted using the provided spin columns resulting in purified, bisulfite-modifed DNA that is ready to use in a wide variety of downstream applications. Key Features Input sample to modified DNA in 90 minutes Conversion efficiencies of 99.9% Effective with as little as 1 ng input DNA Recover modified DNA in as little as 25 microliters Proven performance in multiple downstream applications
Materials Required but Not Delivered	Equipment and Supplies Thermal cycler, heat block, or water bath Microcentrifuge (capable of 12,000 x g) Screw-cap microcentrifuge tubes, 1.5-2.0 mL Narrow range pH indicator paper (pH 0-6, three different indicators per strip, and/or pH 4-7, one indicator per strip) or a dedicated pH electrode). Pipettes and pipette tips (aerosol barrier tips are suggested to minimize potential cross contamination). Analytical scale or balance Reagents Nuclease-free water 96-100% Molecular Biology Grade Ethanol 12 N HCl 3 N NaOH
Background Information	Methylation of cytosines located 5' to guanosine is known to have a profound effect on the expression of many eukaryotic genes. In normal cells methylation occurs predominantly in CG-poor regions, while CG-rich areas, called CpG-islands remain unmethylated. The exceptions are the extensive methylation of CpG islands associated with transcriptional inactivation of regulatory regions of imprinted genes and genes on the inactive X-chromosome of females. Aberrant methylation of normally unmethylated CpG islands has been documented as a relatively frequent event in immortalized and transformed cells and has been associated with transcriptional inactivation of defined tumor suppressor genes in human cancers. Several methods have been developed to determine the methylation status of cytosine. These include the use of antibodies or protein methyl binding domains, digestion with methylation sensitive, insensitive, or dependent restriction enzymes as in restriction landmark genomic scanning (RLGS), oligonucleotide array hybridization, bisulfite genomic DNA sequencing and Methylation Specific PCR (MSP). Genomic DNA sequencing, although time consuming and labor intensive, offers a more universal detection method. MSP is an established technology for the monitoring of abnormal gene methylation in selected gene sequences. Utilizing small amounts of DNA, this procedure offers sensitive and specific detection of 5-methylcytosine in promoters. It is being exploited to define tumor suppressor gene function, and to provide a new strategy for early tumor detection by interrogating DNA derived from tissues and bodily fluids. The initial step of both bisulfite genomic sequencing and MSP is to perform a bisulfite modification of the DNA sample. In the bisulfite reaction, all unmethylated cytosines are deaminated and sulfonated, converting them to uracils, while 5-methylcytosines remain unaltered. Thus, the sequence of the treated DNA will differ depending on whether the DNA is originally methylated or unmethylated. Also, the initially complementary DNA strands will no longer be complementary after cytosine conversion. Primers for use in MSP can be designed to specifically amplify either a bisulfite-sensitive, unmethylated strand or a bisulfite-resistant, methylated strand, based upon these chemically-induced differences. Millipore offers a selection of CpG Wiz® MSP kits to enable gene-specific analysis by MSP. To learn more about CpG Wiz kits and MSP technology Click here

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Product Information
Components	Bisulfite Conversion Reagent 1 Bisulfite Conversion Reagent 2 Bisulfite Reagent Diluent DNA Binding Buffer Wash Buffer NT3 (Concentrate)* Elution Buffer NE Modified DNA Purification Columns 2 mL Collection Tubes *DNA Wash Buffer requires the addition of 100% Ethanol
HS Code	3822 19 90
Quality Level	MQ100

Applications
Application	The CpGenome Turbo Bisulfite Modification Kit is designed to simplify & streamline the bisulfite modification process. In just 90 minutes go from DNA sample to bisulfite converted DNA ready for analysis.
Application Notes	For MSP primer design, please use the MethPrime software package. Click here

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Safety Information according to GHS

Safety Information

Product Usage Statements
Usage Statement	Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Material Size	50 reactions

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Supplemental Information

Specifications

Global Trade Item Number
Catalog Number	GTIN
S7847	04053252746826

Documentation

CpGenome Turbo Bisulfite Modification Kit SDS

Title
Safety Data Sheet (SDS)

References

Reference overview	Pub Med ID
Characterization of induced tissue-specific stem cells from pancreas by a synthetic self-replicative RNA. Miyagi-Shiohira, C; Nakashima, Y; Kobayashi, N; Saitoh, I; Watanabe, M; Noguchi, H Sci Rep 8 12341 2018 Show Abstract Induced pluripotent stem (iPS) cells have significant implications for overcoming most of the ethical issues associated with embryonic stem (ES) cells. Furthermore, our recent study demonstrated the generation of induced tissue-specific stem (iTS) cells by transient overexpression of the reprogramming factors using a plasmid combined with tissue-specific selection. In this study, we were able to generate RNA-based iTS cells that utilize a single, synthetic, self-replicating VEE-RF RNA replicon expressing four reprogramming factors (OCT4, KLF4, SOX2, and GLIS1). A single VEE-RF RNA transfection into mouse pancreatic tissue resulted in efficient generation of iTS cells from pancreas (iTS-P cells) with genetic markers of endoderm and pancreatic progenitors and differentiation into insulin-producing cells more efficiently than ES cells. Subcutaneous transplantation of iTS-P cells into immunodeficient mice resulted in no teratoma formation. Bisulfite genomic sequencing demonstrated that the promoters of Oct4 and Nanog remained partially methylated in iTS-P cells. We compared the global gene-expression profiles of ES cells, iTS-P cells, and pancreatic islets. Microarray analyses confirmed that the iTS-P cells were similar but not identical to ES cells compared with islets. These data suggest that iTS-P cells are cells that inherit numerous components of epigenetic memory from pancreas cells and acquire self-renewal potential. The generation of iTS cells may have important implications for the clinical application of stem cells.	30120295

Reference overview

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User Guides

Title
CpGenome¿ Turbo Bisulfite Modification Kit (50 Reactions) Manual

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