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FAQs

  • How do I remove high molecular weight products in my library?
  • 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 Tapestri Platform detect mitochondrial DNA?
  • Which cell-counting method should I use?
  • How long can I store my emulsions before proceeding?
  • How long can I store Tapestri libraries?
  • What if I load > 4,000 cells per μL onto the cartridge?
  • Why is 1 sample partitioned into 8 tubes after Barcoding?
  • 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 if the Bead volume is > 120 μL after Barcoding?
  • What causes low emulsion quality, how do I identify it?
  • What causes low emulsion volume in the collection tube?
  • Why are DNA concentrations low/high after first PCR?
  • How long from sample to sequence-ready libraries?
  • Does DNA concentration correlate with cell number?
  • When should I pool my technical replicates?
  • Can I use fewer than 100,000 cells in 35 μL?
  • Why are concentrations low after Library PCR?
  • Should I run a control for my unknown patient sample?
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