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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?
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