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A versatile sequencing kit optimised for modal raw read accuracy of Q20+ (99%+) with long read singleplex samples. Multiple samples can be processed simultaneously.
This uses our latest Kit 14 chemistry
This kit is recommended for users who:
Please note that to use this kit, you will need to purchase additional 3rd party reagents: see the «3rd Party Materials» tab for more detail.
| Feature | Property |
|---|---|
| Preparation time | ~60 minutes manually |
| Input requirement | 1 ug of gDNA or 100-200 fmol of amplicons or cDNA |
| PCR Required | No |
| Fragmentation | Optional; recommended for inputs of 100-500 ng |
| Kit chemistry | Kit 14 (V14) |
| Read length | Equal to fragment length |
| Associated protocols | • Ligation Sequencing gDNA (SQK-LSK114-XL) |
| Multiplexing options | • Native Barcoding Kit 24 V14 (SQK-NBD114.24) |
| Pack size | 48 reactions |
| Stability | Shipped at 2–8°C
Long-term storage -20°C Oxford Nanopore Technologies deem the useful life of the product to be 3 months from receipt by the customer |
The Ligation Sequencing Kit XL V14 offers a flexible method of preparing sequencing libraries from dsDNA (e.g. gDNA, cDNA or amplicons). The library preparation method is straightforward: DNA ends are repaired and dA-tailed using the NEBNext End Repair/dA-tailing module before the sequencing adapters, supplied in the kit, are ligated onto the prepared ends.
The kit is optimised to achieve sequencing accuracies of over 99% (Q20+) with high output on our latest nanopore: R10.4.1. Our flow cell priming and sequencing reagents have been reformulated to be compatible with this improved Kit 14 adapter and R10.4.1 nanopore.
Kit 14 also includes previous updates such as the higher capture rate of DNA to enable lower flow cell loading amounts, and fuel fix technology, allowing users to run longer experiments without the need for fuel addition during the run.
Users can either start with 1 μg of gDNA or 100-200 fmol of shorter-fragment input such as amplicons or cDNA. If your experiment requires long reads, it is recommended to start with full-length gDNA, and fragmentation/shearing is not advised. Please note: if long reads are required, high molecular weight DNA should be used as input. To determine purity, we suggest using the Nanodrop to measure the A260/280 and A260/230 ratios and we recommend that the sample should meet the following criteria:
The Ligation Sequencing Kit V14 is compatible with upstream processes such as target enrichment by sequence capture, whole genome amplification (for applications where under 1 ng of sample is available) and size selection (for enrichment of specified fragment lengths, using our Short Fragment Eliminator kit (EXP-SFE001)).
A) Read lengths observed when HMW gDNA was prepared using the Ligation Sequencing Kit with and without size selection (EXP-SFE001 treatment). B) Read N50 observed under the same sequencing conditions, demonstrating significant increase when size selected using EXP-SFE001.
PCR- and WGA-free workflows remove amplification bias and retain base modification information, which can be analysed using tools supported by Oxford Nanopore.
Starting with lower amounts of input material, or impure samples, can affect library preparation efficiency and can reduce sequencing throughput. PCR can be used to generate more input material in cases where sample amount is limiting.
Flow cells and kits are shipped together in an environmentally friendly temperature-controlled shipping box.
Products are shipped to customers within the USA and EU Monday to Thursday. Shipments to Canada, Norway, Korea and Japan are expedited Monday to Wednesday; with Australia and New Zealand leaving our warehouses on a Friday. Shipments to the rest of the world are made on Mondays to allow the full working week for packages to arrive.
The delivery charges are calculated when a quote is raised or during checkout. Once an order is made, the delivery ID and delivery information can be tracked in the Store.
The Ligation Sequencing Kit offers a flexible method of preparing sequencing libraries from dsDNA (e.g. gDNA, cDNA or amplicons). The library preparation method is straightforward: DNA ends are FFPE repaired and end-prepped/dA-tailed using the NEBNext End Repair/dA-tailing module, and then sequencing adapters, supplied in the kit, are ligated onto the prepared ends.
To access the protocol, you will need to register for a Nanopore Community account.
English Safety Data Sheet for Ligation Sequencing Kit XL V14 (SQK-LSK114-XL)
Spanish Safety Data Sheet for Ligation Sequencing Kit XL V14 (SQK-LSK114-XL)
The Ligation Sequencing Kit XL V14 contains sufficient reagents to generate 48 sequencing libraries.
| Name | Acronym | Vial colour | Number of vials | Fill volume per vial (µl) |
|---|---|---|---|---|
| DNA Control Strand | DCS | Yellow | 1 | 100 |
| Ligation Adapter | LA | Green | 1 | 320 |
| Ligation Buffer | LNB | White | 1 | 1,500 |
| Elution Buffer | EB | Clear cap, black label | 1 | 10,000 |
| Long Fragment Buffer | LFB | Clear cap, orange label | 2 | 20,000 |
| Short Fragment Buffer | SFB | Clear cap, dark blue label | 2 | 20,000 |
| Library Beads | LIB | Pink | 2 | 1,800 |
| Library Solution | LIS | White cap, pink label | 2 | 1,800 |
| Sequencing Buffer | SB | Red | 3 | 1,700 |
| Flow Cell Flush | FCF | Clear cap, light blue label | 4 | 15,500 |
| Flow Cell Tether | FCT | Purple | 1 | 1,600 |
The Ligation Sequencing Kit V14 can be used together with:
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