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NGS Library Preparation (NEBNext Ultra II) moderate

Residual Adaptor or Primers After PCR

Symptom
Adaptor or primer peaks visible on Bioanalyzer or similar instrument after PCR amplification, indicating inefficient cleanup or excess reagent usage.
Common Causes
  1. 1 Excess adaptor used during ligation step relative to sample input
  2. 2 Excess PCR primer added or inefficient post-PCR cleanup
  3. 3 SPRI bead cleanup ratio insufficient to remove small adaptor/primer fragments
Solutions
  1. 1 Perform another 0.9X SPRI bead cleanup to remove residual adaptors and primers
  2. 2 Optimize adaptor concentration during ligation based on input amount
  3. 3 Verify correct PCR primer volume is being added according to manual specifications
Related Video (3)
New England Biolabs ★ 92
NEBNext Ultra II DNA Library Prep Protocol
"Direct protocol walkthrough for the exact NEBNext Ultra II DNA Library Prep kit cited in the failure case."
New England Biolabs ★ 78
12 Quick Tips for NGS Library Preparation
"Quick tips for NGS library prep that cover common pitfalls like adaptor/cleanup issues and reagent ratios."
Illumina ★ 65
How can I tell if I sequenced through the insert? Part 1 | Illumina Video
"Demonstrates reading Bioanalyzer traces to interpret library size distribution and artifacts."
Source: neb.com ↗
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