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Videos
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User Guides
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FAQs
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Why do I have to remove oil from my emulsion tubes?
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How do I remove excess primer dimers?
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Which cell-counting method should I use?
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How long can I store my emulsions before proceeding?
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How long can I store Tapestri libraries?
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What if I load > 4,000 cells per μL onto the cartridge?
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Why is 1 sample partitioned into 8 tubes after Barcoding?
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Can I proceed if the volume of the 8 tubes are uneven?
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What are the DNA concentrations for Tapestri libraries?
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Which thermal cyclers should I use for Tapestri DNA?
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Can I use Tapestri reagents for bulk-control experiments?
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Can multiple samples be processed simultaneously?
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Can I replace emulsion collection tubes/gel loading tips?
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What if the Bead volume is > 120 μL after Barcoding?
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What causes low emulsion quality, how do I identify it?
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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?
-
Do I need to clean DNA libraries with off-target products?
-
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?
-
Why do I have to remove oil from my emulsion tubes?
-
Videos
-
User Guides
-
FAQs
-
Why do I have to remove oil from my emulsion tubes?
-
How do I remove excess primer dimers?
-
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?
-
Do I need to clean DNA libraries with off-target products?
-
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?
-
Why do I have to remove oil from my emulsion tubes?