SeqCap Epi Developer Enrichment Kit

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Overview

The SeqCap Epi Developer Enrichment Kits, as part of the SeqCap Epi Enrichment System, enables the targeting of selected genomic regions from bisulfite treated genomic DNA in a single workflow for your genome of interest.

Description Catalog Number Pack Size
SeqCap Epi Developer S Enrichment Kits 07139071001 12 Reactions
SeqCap Epi Developer S Enrichment Kits 07139080001 48 Reactions
SeqCap Epi Developer S Enrichment Kits 07139098001 384 Reactions
SeqCap Epi Developer M Enrichment Kits 07139101001 12 Reactions
SeqCap Epi Developer M Enrichment Kits 07139128001 48 Reactions
SeqCap Epi Developer M Enrichment Kits 07139578001 384 Reactions
SeqCap Epi Developer L Enrichment Kits 07139586001 12 Reactions
SeqCap Epi Developer L Enrichment Kits 07139594001 48 Reactions
SeqCap Epi Developer L Enrichment Kits 07139608001 384 Reactions
SeqCap Epi Developer XL Enrichment Kits 07139624001 12 Reactions
SeqCap Epi Developer XL Enrichment Kits 07139659001 48 Reactions
SeqCap Epi Developer XL Enrichment Kits 07139667001 384 Reactions

For life science research only. Not for use in diagnostic procedures.

Please Contact Us for ordering and questions


Description

Built on Roche NimbleGen’s industry-leading proprietary probe design and manufacturing technologies, the SeqCap Epi Developer Enrichment Kits are customizable probe pools that can target both strands of any organisms’ bisulfite treated genomic DNA.

Benefits

  • Discover differential methylation efficiently: Target your region of interest, up to 210Mb, in the epigenome with the only custom enrichment solution for bisulfite sequencing, delivering better depth of coverage and higher resolution than Whole Genome Bisulfite Sequencing.
  • Optimized design and workflow to effectively conserve epigenome complexity: The SeqCap Epi System’s advanced design algorithm coupled with the ability to manufacture millions of long oligonucleotide probes delivers superior target enrichment performance, which enables you to observe methylation changes on both strands while preserving the ability to decipher between SNPs vs. methylation events, with an industry leading sample input of just 1ug.
  • Maximize epigenetic discovery while minimizing sequencing costs: Reduce the sequencing output needed to verify methylation landscapes potentially responsible for disease and development by focusing on your region of interest.
seqcap_epi_figure1_probe_pool

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SeqCap HE-Oligo Kit A
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