Cat #: 11-338S

Zymo Research D5032 EZ-96 DNA Methylation-Lightning Kit, Shallow-Well, 2 x 96 Rxns/Unit

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Zymo Research D5032 EZ-96 DNA Methylation-Lightning Kit, Shallow-Well, 2 x 96 Rxns/Unit primary image
Zymo Research D5032 EZ-96 DNA Methylation-Lightning Kit, Shallow-Well, 2 x 96 Rxns/Unit primary image
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Cat #: 11-338S

Zymo Research D5032 EZ-96 DNA Methylation-Lightning Kit, Shallow-Well, 2 x 96 Rxns/Unit

Shallow-Well

2 x 96 Rxns/Unit

Brand: Zymo Research
  • Fastest method for complete, high-throughput (96-well) bisulfite conversion of DNA for methylation analysis.
  • Ready-to-use conversion reagent is added directly to DNA.
  • High-yield, converted DNA is ideal for PCR, MSP, array, bisulfite and Next-Gen sequencing.
  • Conversion Efficiency: >99.5% of non-methylated cytosine residues are converted to uracil; >99.5% protection of methylated cytosines.
  • Optimal DNA Input: Samples containing between 100 pg to 2 µg of DNA. For optimal results, the amount of input DNA should be from 200 to 500 ng.
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Shallow-Well

2 x 96 Rxns/Unit

Brand: Zymo Research
  • Fastest method for complete, high-throughput (96-well) bisulfite conversion of DNA for methylation analysis.
  • Ready-to-use conversion reagent is added directly to DNA.
  • High-yield, converted DNA is ideal for PCR, MSP, array, bisulfite and Next-Gen sequencing.
  • Conversion Efficiency: >99.5% of non-methylated cytosine residues are converted to uracil; >99.5% protection of methylated cytosines.
  • Optimal DNA Input: Samples containing between 100 pg to 2 µg of DNA. For optimal results, the amount of input DNA should be from 200 to 500 ng.

The EZ-96 DNA Methylation-Lightning™ Kit features high-throughput (96-well) bisulfite treatment and conversion of DNA for methylation analysis. Key to the fast workflow is the ready-to-use Lightning Conversion Reagent. No preparation is necessary, simply add this unique reagent to a DNA sample, wait about an hour, and let the reaction proceed to completion. DNA denaturation and bisulfite conversion processes are combined with added heat to facilitate rapid denaturation. Desulphonation and clean-up of the converted DNA is performed using a unique 96-well spin-plate. High yield, converted DNA is ideal for PCR, array, bisulfite and next generation sequencing, etc. 

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