FAQs
- How do I remove High Molecular Weight (HMW) fragments from my DNA or Protein Library?
- Tapestri DNA Library Reamplification Protocol
- How can I help prevent my cell suspensions from clumping?
- What is the recommended storage temperature for primer pools?
- Why do I have to remove oil from my emulsion tubes?
- How do I remove excess primer dimers?
- Can the Tapestri Platform detect mitochondrial DNA?
- Which cell-counting method should I use?
- What if I load too many cells per μL onto the cartridge?
- Can I proceed if the volume of the 8 tubes are uneven?
- What are the DNA concentrations for Tapestri libraries?
- Which thermal cyclers should I use for Tapestri DNA?
- Can I use Tapestri reagents for bulk-control experiments?
- Can multiple samples be processed simultaneously?
- Can I replace emulsion collection tubes/gel loading tips?
- What causes low emulsion quality, how do I identify it?
- Why are DNA concentrations low/high after first PCR?