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Thermo Scientific™ MuSeek Index Set 1, Illumina compatible
Description
MuSeek Index Set 1, Illumina compatible, is designed for generation of indexed genomic DNA libraries for sequencing on the Illumina MiSeq™ and HiSeq™ instruments. The set provides 4 indexed P5 adapters and 6 MuSeek indexed P7 adapters. This enables pooling of up to 24 dual-indexed libraries and conducting multiplexed sequencing analysis. The MuSeek Index Set 1, in combination with MuSeek Library Preparation kit, Illumina compatible, allows fast and simple indexed library construction from 50ng of sample DNA, eliminating the need for physical shearing, end conversion and adapter ligation steps.
Highlights
- Enables sequencing of up to 24 dual-indexed fragment libraries in a single sequencing run.
- Indexed DNA fragment library preparation for next generation sequencing.
- MuSeek Indices M501-4
- MuSeek Indices M701-6
Specifications
Specifications
| Content And Storage | Each kit contains sufficient quantities of division arrested (DA) cells and substrate to assay 1 x 384 well plate. (Other materials are required separately; please refer to the protocol). Includes: o Tango™ CMKLR1-bla U2OS DA cells o LiveBLAzer™-FRET B/G Loading Kit, 70μg o Solution D o Tango™ CMKLR1-bla U2OS Assay Protocol o LiveBLAzer™-FRET B/G Loading Protocol o Certificate of Analysis The Tango™ CMKLR1-bla U2OS DA cells are shipped on dry ice and should be stored in liquid nitrogen immediately upon receipt. |
| Format | Kit |
| Sample Type | DNA |
| Sequencing Type | Genome and DNA Sequencing |
| For Use With (Equipment) | Illumina™ HiSeq 2500, Illumina ™ MiSeq |
| For Use With (Application) | Sequencing |
| Libraries | Fragment Library |
| Product Line | MuSeek |
| Product Type | MuSeek Index Set 1 |
| Quantity | 24 Dual Indices (4 x 6) |
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Frequently Asked Questions (FAQs)
MuSeek is not suitable for ssDNA, as MuA transposase is not able to fragment ssDNA. To use MuSeek, ssDNA should first be converted into dsDNA.
Yes. However for construction of NGS library from PCR amplicons in fragmentation reaction, do not use PCR products shorter than 300 bp. Due to intrinsic features of the transposon technology, a approximately 50 bp drop off is expected in sequencing coverage from each distal end of the amplicon sequence. This can be averted by designing your amplicons to be approximately 100 bases larger than the desired sequencing insert.
No, the recommended sample DNA input should be followed strictly. The MuSeek fragmentation reaction is optimized to yield optimal fragment library lengths at recommended input.
We do not supply specific MuSeek kits for NGS library preparation from RNA samples. However, MuSeek is compatible with double-stranded cDNA substrate.
The ClaSeek technology uses a classical NGS library preparation approach where physically fragmented DNA is end-repaired and platform-specific adapters are added through ligation reaction. MuSeek transposase-based technology simultaneously fragments intact DNA and adds MuA transposon derived DNA sequence which is further used for PCR-based adapter addition step.
For Research Use Only. Not for use in diagnostic procedures.