TruSeq Stranded mRNA Library Prep Kit for NeoPrep Compatible Products

The NeoPrep System normalizes libraries to 10nM. Use the following table to determine insert, concentration, and load size for your system and the resulting expected cluster density. 

  • Dilute the normalized library to the predenature concentration.
  • Denature and dilute the library to the intermediate concentration. Depending on the application, pooling after denaturation and dilution can increase library complexity due to the number of unique molecules present in the final mixture when each library is denatured separately in a larger volume.
  • Load the denatured samples using the pooled denatured samples load size.

System

Insert Size

Predenatured Concentration (nM)

Denatured/Diluted Intermediate Concentration (pM) Pooled Denatured Samples Load (pM)

Expected Cluster Density (mm2)

MiSeq

 

200

10

50 10

1200

NextSeq

200

4

40 2–3

~200

HiSeq 2500 TruSeq v3

 

200

2

20 6–10

700–1000

HiSeq 2500 v4

 

200

2

20 12–15

1250

HiSeq 2500 Rapid Run (v1)

 

200

2

20 6–10

600–1000