NEBNext® Ultra™ II FS DNA Library Prep with Sample Purification Beads
Do you need a faster, more reliable solution for DNA fragmentation and library construction? The NEBNext® Ultra™ II FS DNA Library Prep Kit meets the dual challenges of constructing high quality libraries from ever-decreasing input amounts, and scalability of library construction.
The kit includes a new DNA fragmentation reagent, which is also combined with end repair and dA-tailing reagents, enabling these steps to be performed in the same tube, with no clean-ups or sample loss.
You’ll be thrilled to pieces with the result – a reliable, flexible, high-quality library prep that is fast and scalable.
- Perform fragmentation, end repair and dA-tailing with a single enzyme mix
- Experience reliable fragmentation with a single protocol, regardless of DNA input amount or GC content
- Prepare high quality libraries from a wide range of input amounts: 100 pg–500 ng
- Generate high yields with increased reaction efficiencies and minimized sample loss
- Use with DNA in standard buffers (TE, Tris-HCl) and water
- Save time with a streamlined workflow: ~ 2.5 hours, with < 15 minutes hands-on time
- Vary incubation time to generate a wide range of insert sizes
- Enjoy the reliability of SPRIselect® size selection and clean-up beads, supplied in just the amounts you need
The NEBNex®t Ultra™ II FS DNA Library Prep Kit for Illumina provides a fragmentation system: a fast and reliable solution for DNA fragmentation and library construction. A new DNA fragmentation reagent is combined with end repair and dA-tailing reagents, allowing these steps to be performed in the same tube, with no clean-ups or sample loss. The same fragmentation protocol is used for any input amount (100 pg–500 ng), or GC content. The kit also includes the NEBNext Ultra II Ligation Master Mix for adaptor ligation, the NEBNext Ultra II Q5® Master Mix for uniform, high-fidelity library amplification, and the gold standard SPRIselect size selection and clean-up beads. Please note that adaptors and primers are not included in the kit and are available separately.
- Fragmentation, end repair and dA-tailing reagents in a single enzyme mix
- A single fragmentation protocol, regardless of DNA input amount or GC content
- Input amounts: 100 pg–500 ng
- Input DNA can be in water, Tris or TE
- Workflow: ~ 2.5 hours, with < 15 minutes hands-on time
- Includes SPRIselect size selection and clean-up beads
Also available without SPRIselect beads
View additional data presented at AGBT by Peter Ellis, Senior Staff Scientist at the Wellcome Trust Sanger Institute.
For larger volume requirements, customized and bulk packaging is available by purchasing through the Custom Solutions department at NEB. Please contact email@example.com for further information.
The following reagents are supplied with this product:
Store at (°C) Concentration NEBNext® Ligation Enhancer -20 NEBNext® Ultra™ II Ligation Master Mix -20 NEBNext® Ultra II Q5® Master Mix -20 2 X NEBNext® Ultra™ II FS Enzyme Mix -20 NEBNext® Ultra™ II FS Reaction Buffer -20 TE Buffer (1X) -20
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