Ion AmpliSeq™ HD Library Kit with HD Enhancer
Ion AmpliSeq™ HD Library Kit with HD Enhancer
Ion Torrent™

Ion AmpliSeq™ HD Library Kit with HD Enhancer

The Ion AmpliSeq HD Library Kit with HD Enhancer is designed for the manual generation of Unique Molecular Tag (UMT)-targeted자세히 알아보기
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카탈로그 번호Quantity
A57283
카탈로그 번호 A57283
제품 가격(KRW)
6,389,000
Each
카트에 추가하기
제품 가격(KRW)
6,389,000
Each
카트에 추가하기
The Ion AmpliSeq HD Library Kit with HD Enhancer is designed for the manual generation of Unique Molecular Tag (UMT)-targeted amplicon libraries for use as part of the Ion AmpliSeq HD sequencing workflow. This product includes both an Ion AmpliSeq HD Library Kit (Cat. No. A37694) and an HD Enhancer kit for improved library quality and molecular coverage results. It is compatible with custom panels created using the Ion AmpliSeq Designer tool (www.ampliseq.com) and sequenced using an Ion GeneStudio S5 Series instrument.

Ion AmpliSeq HD technology enables scalable polymerase chain reactions (PCRs) from 12- to 5000-plex (1 x 5000-plex in a 1-pool panel or 2 x 2500-plex in a 2-pool panel) for UMT-targeted sequencing, with a level of detection down to 0.1% variant frequency depending on the sample type, sample input amount, and read coverage depth.

Key product features include:
• Custom design creation
• Ultra-high sensitivity detection
• Dual-barcoded sample multiplexing
• Bi-directional sequencing
• Improved library preparation performance

Custom design creation
The Ion AmpliSeq Designer tool can be used to create custom designs for use with Ion AmpliSeq HD technology. The designs are made-to-order and allow the user the flexibility of creating region, hotspot, or fusion designs. These are one- or two-pool designs recommended for use with samples obtained from cfDNA, cfRNA, cfTNA, FFPE DNA, FFPE RNA, gDNA, or total RNA.

Ultra-high sensitivity detection
Ion AmpliSeq HD technology is capable of ultra-high levels of detection down to 0.1%. These detection levels have been observed for cfDNA, cfTNA, and gDNA controls with known variants using an input amount of ≥ 20 ng at adequate read coverage depth. Levels of detection for other sample types, such as FFPE, will vary.

Dual-barcoded sample multiplexing
The Ion AmpliSeq HD Library Kit with HD Enhancer includes reagents for generating amplicons using Ion AmpliSeq HD primers, which are used to prepare libraries for sequencing. The libraries are dual-barcoded at the 5’ and 3’ ends using the Ion AmpliSeq HD Dual Barcode Kit 1-24, which enables the multiplexing of up to 24 samples in a single chip.

Bi-directional sequencing
The Ion AmpliSeq HD Library Kit also provides sequencing information from both strands. This enables better error correction and higher confidence in the quality of your sequence data.

Improved library preparation performance
The new HD Enhancer component included in this kit, in association with an updated Ion AmpliSeq HD library preparation protocol, improves the product performance by reducing primer-dimer formation during library preparation and improving amplicon performance, especially high-GC amplicons molecular coverage.

For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Molecular Tagging, UMT
용도(애플리케이션)Sequencing
용도(장비)Ion GeneStudio™ S5 Series Sequencer
라이브러리Targeted Sequencing Library
반응 수24
핵산 유형cfDNA, cfRNA, CfTNA, FFPE
제품라인AmpliSeq
제품 유형HD Library Kit
샘플 종류DNA/RNA/TNA from plasma or FFPE
배송 조건Dry Ice
워크플로우 단계Library Generation
형식Kit
Sequencing TypeNext Generation Sequencing
Unit SizeEach
구성 및 보관
Store at -5°C to -30°C.

자주 묻는 질문(FAQ)

How long can 10X DNA working panel FWD and REV subpools be stored?

10X DNA working panel FWD and REV subpools can be stored at 4 degrees C for one week. For longer term storage, aliquot and store subpools at -20 degrees C.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

Have there been any recent changes to the protocol for Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283)?

There have been some recent changes to the protocol. Please refer to the latest user guide (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0017392_Ion%20AmpliSeqHDLibraryKit_UG.pdf) for full details.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

When should I use CRC versus HD Enhancer for Ion AmpliSeq HD library preparation?

CRC is a component of the Ion AmpliSeq HD Library Kit (Cat. No. A37694). CRC improves target amplification reactions for challenging panels that produce excessive amounts of primer dimer or panels that have ⋝500 primer pairs. We recommend using CRC with all panel types. HD Enhancer is a component of the Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283) and is also available separately as Cat. No. A53690. HD Enhancer is used for improved library quality and molecular coverage results. Guidelines for using HD Enhancer or CRC for Ion AmpliSeq HD library preparation are outlined in the user guide (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0017392_Ion%20AmpliSeqHDLibraryKit_UG.pdf).

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

Which barcodes are compatible with Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283)?

We recommend using the Ion AmpliSeq HD Dual Barcode Kit 1-24 (Cat. No. A37695) with Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283). The libraries are dual barcoded at the 5' and 3' ends and this enables the multiplexing of up to 24 samples in a single chip. Using these dual barcodes also reduces the risk of barcode cross-contamination.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

What are the shipping and storage conditions for Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283)?

Ion AmpliSeq HD Library Kit with HD Enhancer (Cat. No. A57283) is shipped on dry ice and we recommend storing it at -20 degrees C.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.