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Merck

SEQXI

Sigma-Aldrich

SEQPLEX-I WGA Kit

Whole Genome Amplification, DNA Amplification

Sinónimos:

SeqX-i DNA Amplification kit, The SeqPlex-I DNA Amplification Kit for whole genome amplification (WGA), WGA Kit, Whole Genome Amplification kit

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About This Item

UNSPSC Code:
41121800
NACRES:
NA.55

technique(s)

DNA amplification: suitable
PCR: suitable
whole genome amplification: suitable

compatibility

Illumina Next Generation Sequencing

shipped in

wet ice

storage temp.

−20°C

General description

To order SeqPlexI adapters in tubes, please download NGSO Adapters SeqPlexI tubes (XLSX File). To order arrayed adapters in plates, download NGSO Plate SeqPlexI arrayed plates (XLSX File). Details on our custom adapters product, Next-Gen Sequencing Oligos (NGSO), can be found at SigmaAldrich.com/nextgenoligos. From this page, you can directly access an online ordering configurator by clicking on the "Order Now" option. Both spreadsheets are directly uploadable after selecting the quantity and/or format from the dropdown menus. For adapters in solution in tubes or in plates, NGSO-Silver is the only option available, which has a length cutoff of 60 bases (several of the adapters are longer than 60 bases). In addition, adapters in plates cannot be duplexed. If you would like a feasibility assessment of ordering NGSO-Silver longer 60 bases or duplexed in plates, then please send a request to dnaoligos@milliporesigma.com. All of the adapters are readily available for online ordering if dry and in tubes as either NGSO-Bronze or Gold (recommended purification for any adapter).

Application

SeqPlex-I WGA Kit has been used for whole genome amplification.

Features and Benefits

  • Amplifies fragmented/extremely small quantities of DNA: Yields from ChIP or FFPE, which are 200-500 bp are easily amplified by Random priming technology.
  • Facilitates sequencing from as little as 100 pg of DNA
  • Enhanced primers for complete genome coverage, minimal sequence bias, and amplicon size ideal for next generation sequencing (NGS)
  • Cost-effective: No longer requires an additional NGS library prep step
  • Compatible with Illumina® next-generation sequencing

Components

10X Library Synthesis Solution for SeqXi10X Library Synthesis Buffer for SeqXiLibrary Preparation Enzyme for SeqXi2X Amplification 1 Mix for Seq-IAmplification 1Polymerase for Seq-I5X Amplification 2 Mix for Seq-IAmplification 2 Enzyme for Seq-IDual Index Adapter Primers for Seq-IWater, Molecular Biology Reagent

Other Notes

  • A 20 μL Amplification 2 reaction will produce >100 ng of amplified double-stranded cDNA when starting with 100 pg to 5 ng of high-quality DNA. Higher input quantities and higher quality DNA template generally result in increased yields. For damaged DNA, such as from FFPE, 1–50 ng input DNA is recommended.
  • The dual index adapter primers (AP100) provided in this kit will only work for one sample. If pooling of samples for sequencing is required, the user must provide additional index primer sets. See example index primer sequences on page 2 of the technical bulletin.

Legal Information

Illumina is a registered trademark of Illumina, Inc.
SeqPlex is a trademark of Sigma-Aldrich Co. LLC

Disclaimer

The SeqPlex-I DNA Amplification Kit for whole genome amplification (WGA) is for R&D use only. Not for drug, household, or other uses.

Related product

Referencia del producto
Descripción
Precios

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Storage Class

10 - Combustible liquids


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Artículos

SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.

SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.

SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.

SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.

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