Pool Multiple Library Preparations in a Single Flow Cell Lane
The NEXTFLEX® Bisulfite-Seq Barcodes are designed to be used with the NEXTFLEX® Bisulfite-Seq Kit. Unlike other NEXTFLEX® Barcodes, the NEXTFLEX® Bisulfite-Seq Barcodes are methylated. The NEXTFLEX® Bisulfite-Seq Barcodes can be used to provide flexibility and high-throughput capabilities in sequencing applications. They significantly increase scale while reducing costs by allowing the user to pool multiple library preparations in a single flow cell lane. The NEXTFLEX® Bisulfite-Seq Barcodes kits accomplish this by using an indexed adapter with a 6 nt unique sequence. This allows for proper differentiation between samples, preventing poor reads from single base errors introduced during PCR.
These methylated adapters can be used with single, paired-end and multiplex reads.
产品特点:
- Up to 24 methylated adapters for multiplexing Illumina® RRBS and WGBS libraries are available
- Considerably reduce your per-sample sequencing cost by barcoded multiplexing
- Increase your sequencing scale by pooling samples on a single flow cell
- Compatible with bisulfite-sequencing on the Illumina® sequencing platforms
产品列表:
货号 |
产品名称 |
规格 |
NOVA-511911 |
NEXTFLEX® Bisulfite-Seq Barcodes-6 |
48 RXNS |
NOVA-511912 |
NEXTFLEX® Bisulfite-Seq Barcodes-12 |
96 RXNS |
NOVA-511913 |
NEXTFLEX® Bisulfite-Seq Barcodes-24 |
192 RXNS |
试剂盒组分
- NEXTFLEX® Bisulfite-Seq Adapters (25 µM)
- NEXTFLEX® Primer Mix (12.5 µM)
引用文献
- Agarwal, P., et al. (2015) CGGBP1 mitigates cytosine methylation at repetitive DNA sequences. BMC Genomics, 16:390. doi:10.1186/s12864-015-1593-2.
- Berg, A., et al. (2015) Obesity is Associated With DNA Methylation in Population-Based Adolescents. Circulation. Poster: 131:AP260, Session Title: Obesity.
- Bewick, A., et. al. (2016) On the origin and evolutionary consequences of gene body DNA methylation. PNAS. 113: 9111 – 9116.
- Ramesh, V., et. al. (2016) Loss of Uhrf1 in neural stem cells leads to activation of retroviral elements and delayed neurodegeneration. Genes & Development. 30: 2199 – 2212.
- Satgé, C. et. al. (2016) Reprogramming of DNA methylation is critical for nodule development in Medicago truncatula. Nature Plants 2, 16166. doi:10.1038/nplants.2016.166.
- Urich, M. A., Nery, J. R., Lister, R., Schmitz, R. J. and Ecker, J. R. (2015) MethylC-seq library preparation for base-resolution whole-genome bisulfite sequencing. Nature Protocols 10, 475–483. doi:10.1038/nprot.2014.114.
- van der Graafa, A., et al. (2015) Rate, spectrum, and evolutionary dynamics of spontaneous epimutations. PNAS. 112:21. pg. 6676–6681. doi: 10.1073/pnas.1424254112.
- Ye, R., et al. (2015) A Dicer-Independent Route for Biogenesis of siRNAs that Direct DNA Methylation in Arabidopsis. Molecular Cell. doi:10.1016/j.molcel.2015.11.015.
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技术服务:
1、DAP-seq:高通量检测转录因子或DNA结合蛋白在基因组上的结合位点。
2、酵母单杂交:研究
蛋白质和特定
DNA序列相互作用。
3、酵母双杂交:检测已知蛋白质之间的相互作用,鉴定与已知蛋白相互作用的未知蛋白。
4、EMSA:鉴定或验证DNA结合蛋白和DNA序列的相互作用。
5、ChIP-seq:高效检测重组蛋白、转录因子在基因组的结合位点。
6、DAP-seq与RNA-seq联合分析: 分析转录因子的靶基因在RNA-seq数据中的表达变化,深入挖掘DAP-seq和RNA-seq测序数据,增加转录组测序的分析深度。
7、DNA-pull down:鉴定与DNA结合的蛋白。
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