
u
For single-indexed runs on a single-read flow cell—FDR and HP12
u
For dual-indexed runs on a single-read flow cell—FDR, HP9, and HP12
2
Thaw reagents in a room temperature deionized water bath for about 20 minutes.
Prepare FDR and HP12
1
Invert tubes to mix.
2
Centrifuge at 1000 rpm for 1 minute.
3
Set aside at room temperature.
Prepare HP9
1
Invert to mix.
2
Briefly pulse centrifuge to collect droplets.
3
Set aside at room temperature.
Prepare Paired-End Reagents
Paired-end reagents are used during the Read 2 resynthesis step of a paired-end sequencing run.
WARNING
This set of reagents contains potentially hazardous chemicals. Personal injury can occur through inhalation,
ingestion, skin contact, and eye contact. Wear protective equipment, including eye protection, gloves, and
laboratory coat appropriate for risk of exposure. Handle used reagents as chemical waste and discard in
accordance with applicable regional, national, and local laws and regulations. For additional environmental,
health, and safety information, see the SDS at
.
Thaw Paired-End Reagents
1
Remove the following reagents from -25°C to -15°C storage:
u
For non-indexed runs—AMS, FDR, FLM2, FPM, FRM, and HP11
u
For indexed runs—AMS, FLM2, FPM, FRM, and HP11
2
Thaw reagents in a beaker filled with room temperature water for about 20 minutes.
3
Place AMS, FLM2, and FRM on ice.
Prepare AMS, FDR, FLM2, FPM, FRM, and HP11
1
Invert to mix.
2
Centrifuge at 1000 rpm for 1 minute.
3
Set aside AMS, FLM2, and FRM on ice.
4
Set aside FDR, FPM, and HP11 at room temperature.
Enter Run Parameters
Begin run setup by entering run parameters from a series of screens on the Run Configuration tab. The
software guides you through each screen to specify BaseSpace Sequence Hub connectivity, enter
consumable IDs, select indexing options, and record other parameters.
Document # 15011190 v03
For Research Use Only. Not for use in diagnostic procedures.
13
HiSeq 2000 System Guide