NEBNext dA-Tailing Module Protocol (E6053)
Introduction
Starting Material: 1-5 μg of of end repaired, blunt DNA (100-1000 bp).
Protocol
- Mix the following components in a sterile microfuge tube:
End Repaired, Blunt DNA variable NEBNext dA-Tailing Reaction Buffer (10X) 5 μl Klenow Fragment (3´→ 5´ exo–) 3 μl Sterile H2O variable Total volume 50 μl - Incubate in a thermal cycler for 30 minutes at 37°C with the heated lid set to ≥ 45°C.
- Purify DNA sample on one spin column or using AMPure XP beads or SPRIselect beads.
Note: for details how this module is used in the NEBNext Library Prep for Illumina workflow, please see manual for NEBNext DNA library Prep Master Mix Set for Illumina (NEB #E6040).