TruSeq Stranded mRNA Sample Preparation HS EUC and LTF 15031057 E

TruSeq Stranded mRNA Sample Preparation HS EUC and LTF 15031057 E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
FOR RESEARCH USE ONLY
Date: __________________________
Illumina Kit Lot #: __________________________
Description: ______________________________________
_________________________________________________
NOTE
Unless familiar with the HS protocol in the latest version of the TruSeq Stranded mRNA Sample Preparation Guide
(part # 15031047), new or less experienced users are advised to follow the protocol in the guide before using this
Experienced User Card and Lab Tracking Form.
ILLUMINA PROPRIETARY
Catalog # RS-122-9003DOC
Part # 15031057 Rev. E
October 2013
Page 1 of 32
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Page 2 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
Item
Lot Number
A-Tailing Control (CTA)
Lot #: _____________________
A-Tailing Mix (ATL)
Lot #: _____________________
Bead Binding Buffer (BBB)
Lot #: _____________________
Bead Washing Buffer (BWB)
Lot #: _____________________
Elution Buffer (ELB)
Lot #: _____________________
End Repair Control (CTE)
Lot #: _____________________
First Strand Synthesis Act D Mix (FSA)
Lot #: _____________________
Fragment, Prime, Finish Mix (FPF)
Lot #: _____________________
Ligation Control (CTL)
Lot #: _____________________
Ligation Mix (LIG)
Lot #: _____________________
PCR Master Mix (PMM)
Lot #: _____________________
PCR Primer Cocktail (PPC)
Lot #: _____________________
Resuspension Buffer (RSB)
Lot #: _____________________
RNA Purification Beads (RPB)
Lot #: _____________________
Second Strand Marking Master Mix (SMM)
Lot #: _____________________
Stop Ligation Buffer (STL)
Lot #: _____________________
80% Ethanol
Date Prepared: ____________
Adapter Indices or RAP
Lot Number
RNA Adapter Index 1 (AR001)
Lot #: _____________________
RNA Adapter Index 2 (AR002)
Lot #: _____________________
RNA Adapter Index 3 (AR003)
Lot #: _____________________
RNA Adapter Index 4 (AR004)
Lot #: _____________________
RNA Adapter Index 5 (AR005)
Lot #: _____________________
RNA Adapter Index 6 (AR006)
Lot #: _____________________
RNA Adapter Index 7 (AR007)
Lot #: _____________________
RNA Adapter Index 8 (AR008)
Lot #: _____________________
RNA Adapter Index 9 (AR009)
Lot #: _____________________
Part # 15031057 Rev. E
Page 3 of 32
Consumables
Consumables
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Consumables
Date/Time: _______________________________
Adapter Indices or RAP
Operator: _______________________________
Lot Number
RNA Adapter Index 10 (AR010)
Lot #: _____________________
RNA Adapter Index 11 (AR011)
Lot #: _____________________
RNA Adapter Index 12 (AR012)
Lot #: _____________________
RNA Adapter Index 13 (AR013)
Lot #: _____________________
RNA Adapter Index 14 (AR014)
Lot #: _____________________
RNA Adapter Index 15 (AR015)
Lot #: _____________________
RNA Adapter Index 16 (AR016)
Lot #: _____________________
RNA Adapter Index 18 (AR018)
Lot #: _____________________
RNA Adapter Index 19 (AR019)
Lot #: _____________________
RNA Adapter Index 20 (AR020)
Lot #: _____________________
RNA Adapter Index 21 (AR021)
Lot #: _____________________
RNA Adapter Index 22 (AR022)
Lot #: _____________________
RNA Adapter Index 23 (AR023)
Lot #: _____________________
RNA Adapter Index 24 (AR024)
Lot #: _____________________
RNA Adapter Index 25 (AR025)
Lot #: _____________________
RNA Adapter Index 27 (AR027)
Lot #: _____________________
RNA Adapter Plate, 96plex (RAP)
Lot #: _____________________
Page 4 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process purifies the polyA containing mRNA molecules using poly-T oligo attached
magnetic beads using two rounds of purification. During the second elution of the polyA RNA,
the RNA is also fragmented and primed for cDNA synthesis.
Consumables
Item
Quantity
Storage
Supplied By
Bead Binding Buffer (BBB)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Bead Washing Buffer (BWB)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Elution Buffer (ELB)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Fragment, Prime, Finish Mix
(FPF)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Resuspension Buffer (RSB)
1 tube
-15°C to -25°C
Illumina
RNA Purification Beads (RPB)
1 tube per 48 reactions
2°C to 8°C
Illumina
Barcode labels for:
• RBP (RNA Bead Plate)
• RFP (RNA Fragmentation
Plate)
1 label per plate
15°C to 30°C
Illumina
96-well HSP Plate
1
15°C to 30°C
User
96-well MIDI Plate
1
15°C to 30°C
User
Microseal ‘B’ Adhesive Seals
7
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
6
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
6
15°C to 30°C
User
Make RBP
[_] 1
Dilute the total RNA with nuclease-free ultra pure water to a final volume of 50 µl in the
new 96-well MIDI plate labeled with the RBP barcode.
[_] 2
Vortex the room temperature RNA Purification Beads tube vigorously to resuspend the
oligo-dT beads.
[_] 3
Add 50 µl of RNA Purification Beads to each well of the RBP plate to bind the polyA RNA
to the oligo dT magnetic beads. Mix thoroughly as follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
Part # 15031057 Rev. E
Page 5 of 32
Purify and Fragment mRNA
Purify and Fragment mRNA
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Purify and Fragment mRNA
Date/Time: _______________________________
Operator: _______________________________
Incubate 1 RBP
[_] 1
Place the sealed RBP plate on the pre-heated microheating system. Close the lid and incubate
at 65°C for 5 minutes to denature the RNA and facilitate binding of the polyA RNA to the
beads.
Start time: _____________________
Stop time: _____________________
[_] 2
Remove the RBP plate from the microheating system and place on ice for 1 minute.
[_] 3
Place the RBP plate on the bench and incubate at room temperature for 5 minutes to allow
the RNA to bind to the beads.
Start time: _____________________
[_] 4
Stop time: _____________________
Pre-heat the microheating system to 80°C for the subsequent incubation.
Wash RBP
[_] 1
Remove the adhesive seal from the RBP plate.
[_] 2
Place the RBP plate on the magnetic stand at room temperature for 5 minutes to separate the
polyA RNA bound beads from the solution.
Start time: _____________________
Stop time: _____________________
[_] 3
Remove and discard all of the supernatant from each well of the RBP plate.
[_] 4
Remove the RBP plate from the magnetic stand.
[_] 5
Wash the beads by adding 200 µl of Bead Washing Buffer in each well of the RBP plate to
remove unbound RNA. Mix thoroughly as follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
[_] 6
Remove the adhesive seal from the RBP plate.
[_] 7
Place the RBP plate on the magnetic stand at room temperature for 5 minutes.
Start time: _____________________
Stop time: _____________________
[_] 8
Centrifuge the thawed Elution Buffer to 600 × g for 5 seconds.
[_] 9
Remove and discard all of the supernatant from each well of the RBP plate.
[_] 10 Remove the RBP plate from the magnetic stand.
[_] 11 Add 50 µl of Elution Buffer in each well of the RBP plate. Mix thoroughly as follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
[_] 12 Store the Elution Buffer tube at 4°C.
Incubate 2 RBP
[_] 1
Place the sealed RBP plate on the pre-heated microheating system. Close the lid and incubate
at 80°C for 2 minutes to elute the mRNA from the beads.
Start time: _____________________
Stop time: _____________________
Page 6 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
Remove the RBP plate from the microheating system and place on ice for 1 minute.
[_] 3
Place the RBP plate on the bench at room temperature.
[_] 4
Remove the adhesive seal from the RBP plate.
Make RFP
[_] 1
Centrifuge the thawed Bead Binding Buffer to 600 × g for 5 seconds.
[_] 2 Add 50 µl of Bead Binding Buffer to each well of the RBP plate. Mix thoroughly as follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
[_] 3
Incubate the RBP plate at room temperature for 5 minutes and store the Bead Binding Buffer
tube at 2°C to 8°C.
[_] 4
Remove the adhesive seal from the RBP plate.
[_] 5
Place the RBP plate on the magnetic stand at room temperature for 5 minutes.
Start time: _____________________
Stop time: _____________________
[_] 6
Remove and discard all of the supernatant from each well of the RBP plate.
[_] 7
Remove the RBP plate from the magnetic stand.
[_] 8
Wash the beads by adding 200 µl of Bead Washing Buffer in each well of the RBP plate. Mix
thoroughly as follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
[_] 9
Store the Bead Washing Buffer tube at 2°C to 8°C.
[_] 10 Remove the adhesive seal from the RBP plate.
[_] 11 Place the RBP plate on the magnetic stand at room temperature for 5 minutes.
Start time: _____________________
Stop time: _____________________
[_] 12 Remove and discard all of the supernatant from each well of the RBP plate.
[_] 13 Remove the RBP plate from the magnetic stand.
[_] 14 Add 19.5 µl of Fragment, Prime, Finish Mix to each well of the RBP plate. Mix thoroughly as
follows:
[_] a Seal the RBP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the RBP plate on a microplate shaker continuously at 1000 rpm for 1 minute.
[_] 15 Remove the adhesive seal from the RBP plate.
[_] 16 Transfer the entire contents from each well of the RBP plate to the corresponding well of the
new HSP plate labeled with the RFP barcode.
[_] 17 Seal the RFP plate with a Microseal ‘B’ adhesive seal.
[_] 18 Store the Fragment, Prime, Finish Mix tube at -15°C to -25°C.
Part # 15031057 Rev. E
Page 7 of 32
Purify and Fragment mRNA
[_] 2
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Purify and Fragment mRNA
Date/Time: _______________________________
Operator: _______________________________
Incubate RFP
[_] 1
Place the sealed RFP plate on the pre-programmed thermal cycler. Close the lid and select
Elution 2 - Frag - Prime (94°C for 8 minutes, 4°C hold) to elute, fragment, and prime the
RNA.
[_] 2
Remove the RFP plate from the thermal cycler when it reaches 4°C and centrifuge briefly.
[_] 3
Proceed immediately to Synthesize First Strand cDNA on page 9.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Page 8 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process reverse transcribes the cleaved RNA fragments that were primed with random
hexamers into first strand cDNA using reverse transcriptase and random primers. The addition
of Actinomycin D to the First Stand Synthesis Act D mix (FSA) prevents spurious DNAdependent synthesis, while allowing RNA-dependent synthesis, improving strand specificity.
Consumables
Item
Quantity
Storage
Supplied By
First Strand Synthesis Act D Mix
(FSA)
1 tube
-15°C to -25°C
Illumina
CDP (cDNA Plate) Barcode Label
1 label per plate
15°C to 30°C
Illumina
96-well HSP Plate
1
15°C to 30°C
User
Microseal ‘B’ Adhesive Seal
1
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
1
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
1
15°C to 30°C
User
SuperScript II Reverse
Transcriptase
1 tube
-15°C to -25°C
User
Make CDP
[_] 1
Remove the adhesive seal from the RFP plate.
[_] 2
Place the RFP plate on the magnetic stand at room temperature for 5 minutes. Do not
remove the plate from the magnetic stand.
Start time: _____________________
Stop time: _____________________
[_] 3
Transfer 17 µl supernatant from each well of the RFP plate to the corresponding well of the
new HSP plate labeled with the CDP barcode.
[_] 4
Centrifuge the thawed First Strand Synthesis Act D Mix tube to 600 × g for 5 seconds.
[_] 5
Add 50 µl SuperScript II to the First Strand Synthesis Act D Mix tube. Mix gently, but
thoroughly and centrifuge briefly. If you are not using the entire contents of the First Strand
Synthesis Act D Mix tube, add SuperScript II at a ratio of 1 µl SuperScript II for each
9 µl First Strand Synthesis Act D Mix.
Label the First Strand Synthesis Act D Mix tube to indicate that the SuperScript II has been
added.
[_] 6
Add 8 µl of First Strand Synthesis Act D Mix and SuperScript II mix to each well of the
CDP plate. Mix thoroughly as follows:
[_] a Seal the CDP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CDP plate on a microplate shaker continuously at 1,600 rpm for 20 seconds.
Part # 15031057 Rev. E
Page 9 of 32
Synthesize First Strand cDNA
Synthesize First Strand cDNA
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Synthesize First Strand cDNA
Date/Time: _______________________________
[_] 7
Operator: _______________________________
Return the First Strand Synthesis Act D Mix tube to -15°C to -25°C storage immediately after
use.
Incubate 1 CDP
[_] 1
Place the sealed CDP plate on the pre-programmed thermal cycler. Close the lid, and then
select and run the Synthesize 1st Strand program.
[_] a Choose the pre-heat lid option and set to 100°C
[_] b 25°C for 10 minutes
[_] c 42°C for 15 minutes
[_] d 70°C for 15 minutes
[_] e Hold at 4°C
[_] 2
When the thermal cycler reaches 4°C, remove the CDP plate from the thermal cycler and
proceed immediately to Synthesize Second Strand cDNA on page 11.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Page 10 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process removes the RNA template and synthesizes a replacement strand, incorporating
dUTP in place of dTTP to generate ds cDNA. The incorporation of dUTP quenches the second
strand during amplification, because the polymerase does not incorporate past this nucleotide.
AMPure XP beads are used to separate the ds cDNA from the second strand reaction mix. At the
end of this process, you have blunt-ended cDNA.
Consumables
Item
Quantity
Storage
Supplied By
(Optional) End Repair Control
(CTE)
1 tube per 48 reactions
2°C to 8°C
Illumina
Resuspension Buffer (RSB)
1 tube
2°C to 8°C
Illumina
Second Strand Marking Master
Mix (SMM)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Barcode labels for:
• ALP (Adapter Ligation Plate)
• CCP (cDNA Clean Up Plate)
• IMP (Insert Modification Plate)
1 label per plate
15°C to 30°C
Illumina
96-well MIDI Plates
2
15°C to 30°C
User
AMPure XP Beads
90 µl per sample
2°C to 8°C
User
Freshly Prepared 80% Ethanol
(EtOH)
400 µl per sample
15°C to 30°C
User
Microseal ‘B’ Adhesive Seals
4
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
5
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
5
15°C to 30°C
User
Add SMM
[_] 1
Remove the adhesive seal from the CDP plate.
[_] 2
Do one of the following:
• If using the in-line control reagent:
— Centrifuge the thawed End Repair Control tube to 600 × g for 5 seconds.
— Dilute the End Repair Control to 1/50 in Resuspension Buffer (For example, 2 µl End
Repair Control + 98 µl Resuspension Buffer) before use.
— Add 5 µl of diluted End Repair Control to each well of the CDP plate.
• If not using the in-line control reagent, add 5 µl of Resuspension Buffer to each well of
the CDP plate.
Part # 15031057 Rev. E
Page 11 of 32
Synthesize Second Strand cDNA
Synthesize Second Strand cDNA
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Synthesize Second Strand cDNA
Date/Time: _______________________________
[_] 3
Operator: _______________________________
Centrifuge the thawed Second Strand Marking Master Mix to 600 × g for 5 seconds.
[_] 4
Add 20 µl of thawed Second Strand Marking Master Mix to each well of the CDP plate. Mix
thoroughly as follows:
[_] a Seal the CDP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CDP plate on a microplate shaker continuously at 1600 rpm for 20 seconds.
[_] 5
Return the Second Strand Marking Master Mix tube to -15°C to -25°C storage after use.
Incubate 2 CDP
[_] 1
Place the sealed CDP plate on the pre-heated thermal cycler. Close the lid and incubate at
16°C for 1 hour.
Start time: _____________________
Stop time: _____________________
[_] 2
Remove the CDP plate from the thermal cycler and place it on the bench.
[_] 3
Remove the adhesive seal from the CDP plate.
[_] 4
Let the CDP plate stand to bring it to room temperature.
Purify CDP
[_] 1
Vortex the AMPure XP beads until they are well dispersed.
[_] 2
Add 90 µl of well-mixed AMPure XP beads to each well of the new MIDI plate labeled with
the CCP barcode.
[_] 3
Transfer the entire contents from each well of the CDP plate to the corresponding well of the
CCP plate containing AMPure XP beads. Mix thoroughly as follows:
[_] a Seal the CCP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CCP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 4
Incubate the CCP plate at room temperature for 15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 5
Centrifuge the CCP plate to 280 × g for 1 minute.
[_] 6
Remove the adhesive seal from the CCP plate.
[_] 7
Place the CCP plate on the magnetic stand at room temperature, for 5 minutes to make sure
that all of the beads are bound to the side of the wells.
Start time: _____________________
Stop time: _____________________
[_] 8
Remove and discard 135 µl supernatant from each well of the CCP plate.
[_] 9
With the CCP plate on the magnetic stand, add 200 µl freshly prepared 80% EtOH to each
well without disturbing the beads.
[_] 10 Incubate the CCP plate at room temperature for 30 seconds, and then remove and discard all
of the supernatant from each well.
[_] 11 Repeat steps 9 and 10 one time for a total of two 80% EtOH washes.
[_] 12 Let the CCP plate stand at room temperature for 15 minutes to dry, and then remove the
plate from the magnetic stand.
Start time: _____________________
Stop time: _____________________
Page 12 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
Start time: _____________________
Stop time: _____________________
[_] 14 Add 17.5 µl Resuspension Buffer to each well of the CCP plate. Mix thoroughly as follows:
[_] a Seal the CCP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CCP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 15 Incubate the CCP plate at room temperature for 2 minutes.
Start time: _____________________
Stop time: _____________________
[_] 16 Centrifuge the CCP plate to 280 × g for 1 minute.
[_] 17 Remove the adhesive seal from the CCP plate.
[_] 18 Place the CCP plate on the magnetic stand at room temperature for 5 minutes.
Start time: _____________________
Stop time: _____________________
[_] 19 Transfer 15 µl supernatant (ds cDNA) from the CCP plate to the new MIDI plate labeled
with the ALP barcode.
SAFE STOPPING POINT
If you do not plan to proceed immediately to Adenylate 3' Ends on page 15, you can safely stop the
protocol here. If you are stopping, seal the ALP plate with a Microseal ‘B’ adhesive seal and store at
-15°C to -25°C for up to seven days.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Part # 15031057 Rev. E
Page 13 of 32
Synthesize Second Strand cDNA
[_] 13 Centrifuge the thawed, room temperature Resuspension Buffer to 600 × g for 5 seconds.
TruSeq Stranded mRNA Sample Prep HS Protocol
Synthesize Second Strand cDNA
Experienced User Card and Lab Tracking Form
Page 14 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
A single ‘A’ nucleotide is added to the 3’ ends of the blunt fragments to prevent them from
ligating to one another during the adapter ligation reaction. A corresponding single
‘T’ nucleotide on the 3’ end of the adapter provides a complementary overhang for ligating the
adapter to the fragment. This strategy ensures a low rate of chimera (concatenated template)
formation.
Consumables
Item
Quantity
Storage
Supplied By
(Optional) A-Tailing Control
(CTA)
1 tube per 48 reactions
-15°C to -25°C
Illumina
A-Tailing Mix (ATL)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Resuspension Buffer (RSB)
1 tube
2°C to 8°C
Illumina
Ice
As needed to place a
plate on
-15°C to -25°C
User
Microseal ‘B’ Adhesive Seal
1
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
3
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
3
15°C to 30°C
User
Add ATL
[_] 1
Do one of the following:
• If using the in-line control reagent:
— Centrifuge the thawed A-Tailing Control tube to 600 × g for 5 seconds.
— Dilute the A-Tailing Control to 1/100 in Resuspension Buffer (For example, 1 µl
A-Tailing Control + 99 µl Resuspension Buffer) before use. Discard the diluted
A-Tailing Control after use.
— Add 2.5 µl of diluted A-Tailing Control to each well of the ALP plate.
• If not using the in-line control reagent, add 2.5 µl of Resuspension Buffer to each well of
the ALP plate.
[_] 2
Add 12.5 µl of thawed A-Tailing Mix to each well of the ALP plate. Mix thoroughly as
follows:
[_] a Seal the ALP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the ALP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 3
Centrifuge the ALP plate to 280 × g for 1 minute.
Part # 15031057 Rev. E
Page 15 of 32
Adenylate 3' Ends
Adenylate 3' Ends
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Adenylate 3' Ends
Date/Time: _______________________________
Operator: _______________________________
Incubate 1 ALP
[_] 1
Place the sealed ALP plate on the pre-heated microheating system 1. Close the lid and
incubate at 37°C for 30 minutes.
Start time: _____________________
[_] 2
Stop time: _____________________
Immediately after the 37°C incubation, remove the ALP plate from system 1 and place the
plate on the pre-heated microheating system 2. Close the lid and incubate at 70°C for
5 minutes.
Start time: _____________________
Stop time: _____________________
[_] 3
Set the microheating system 1 to 30°C in preparation for Ligate Adapters.
[_] 4
Immediately remove the ALP plate from the microheating system 2 and place the plate on
ice for 1 minute.
[_] 5
Proceed immediately to Ligate Adapters on page 17.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Page 16 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process ligates indexing adapters to the ends of the ds cDNA, preparing them for
hybridization onto a flow cell.
Consumables
Item
Quantity
Storage
Supplied By
(Optional) Ligation Control (CTL)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Choose from the following
depending on the kit you are
using:
• TruSeq Stranded mRNA LT
Sample Prep Kit contents:
• RNA Adapter Indices
(AR001–AR016, AR018–
AR023, AR025, AR027)
• TruSeq Stranded mRNA HT
Sample Prep Kit contents:
• RAP (RNA Adapter Plate)
1 tube of each index
being used, per
column of 8 reactions
or
1 RAP
-15°C to -25°C
Illumina
Ligation Mix (LIG)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Resuspension Buffer (RSB)
1 tube
2°C to 8°C
Illumina
Stop Ligation Buffer (STL)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Barcode labels for:
• CAP (Clean Up ALP Plate)
• PCR (Polymerase Chain
Reaction Plate)
• RAP (RNA Adapter Plate)
(if using the HT kit)
1 label per plate
15°C to 30°C
Illumina
96-well HSP Plate
1
15°C to 30°C
User
96-well MIDI Plate
1
15°C to 30°C
User
AMPure XP Beads
92 µl per sample
2°C to 8°C
User
Freshly Prepared 80% Ethanol
(EtOH)
800 µl per sample
15°C to 30°C
User
Microseal ‘B’ Adhesive Seals
7
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
4–28
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
4–28
15°C to 30°C
User
Part # 15031057 Rev. E
Page 17 of 32
Ligate Adapters
Ligate Adapters
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Ligate Adapters
Date/Time: _______________________________
Operator: _______________________________
Add LIG
[_] 1
Do one of the following:
• If using RNA Adapter tubes, centrifuge the thawed tubes to 600 × g for 5 seconds.
• If using a RAP:
— Thaw the plate for 10 minutes at room temperature on the benchtop. Visually
inspect the wells to make sure that they all are thawed.
Start time: _____________________
Stop time: _____________________
— Remove the adapter plate tape seal.
— Centrifuge the plate to 280 × g for 1 minute to collect all of the adapter to the bottom
of the well.
— Remove the plastic cover. Save the cover if you are not processing the entire plate at
one time.
— If it is the first time using this RAP, apply the RAP barcode label to the plate.
NOTE
• The RAP is single-use for each well.
• Illumina recommends that the RAP does not undergo more than 4 freeze-thaw cycles.
[_] 2
Centrifuge the Ligation Control (if using Ligation Control) and Stop Ligation Buffer tubes to
600 × g for 5 seconds.
[_] 3
Immediately before use, remove the Ligation Mix tube from -15°C to -25°C storage.
[_] 4
Remove the adhesive seal from the ALP plate.
[_] 5
Do one of the following:
• If using the in-line control reagent:
— Dilute the Ligation Control to 1/100 in Resuspension Buffer (For example, 1 µl
Ligation Control + 99 µl Resuspension Buffer) before use. Discard the diluted
Ligation Control after use.
— Add 2.5 µl of diluted Ligation Control to each well of the ALP plate.
• If not using the in-line control reagent, add 2.5 µl of Resuspension Buffer to each well of
the ALP plate.
[_] 6
Add 2.5 µl of Ligation Mix to each well of the ALP plate.
[_] 7
Return the Ligation Mix tube to -15°C to -25°C storage immediately after use.
[_] 8
Do one of the following:
• If using RNA Adapter tubes, add 2.5 µl of the thawed RNA Adapter Index to each well
of the ALP plate.
• If using a RAP:
— Place the RAP on the benchtop so that the part number barcode, on the long side of
the plate, is facing you and the clipped corner is on the lower left.
Page 18 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
[_] 9 Mix thoroughly as follows:
[_] a Seal the ALP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the ALP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 10 Centrifuge the ALP plate to 280 × g for 1 minute.
Incubate 2 ALP
[_] 1
Place the sealed ALP plate on the pre-heated microheating system. Close the lid and
incubate at 30°C for 10 minutes.
Start time: _____________________
[_] 2
Stop time: _____________________
Remove the ALP plate from the microheating system.
Add STL
[_] 1
Remove the adhesive seal from the ALP plate.
[_] 2
Add 5 µl of Stop Ligation Buffer to each well of the ALP plate to inactivate the ligation mix.
Mix thoroughly as follows:
[_] a Seal the ALP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the ALP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 3
Centrifuge the ALP plate to 280 × g for 1 minute.
Clean Up ALP
[_] 1
Remove the adhesive seal from the ALP plate.
[_] 2
Vortex the AMPure XP Beads for at least 1 minute or until they are well dispersed.
[_] 3
Add 42 µl of mixed AMPure XP Beads to each well of the ALP plate. Mix thoroughly as
follows:
[_] a Seal the ALP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the ALP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 4
Incubate the ALP plate at room temperature for 15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 5
Centrifuge the ALP plate to 280 × g for 1 minute.
[_] 6
Remove the adhesive seal from the ALP plate.
Part # 15031057 Rev. E
Page 19 of 32
Ligate Adapters
— Do one of the following to pierce the foil seal:
— If using the entire plate at one time, use the bottom of a clean 96-well semiskirted PCR plate to pierce a hole in all of the well seals simultaneously. Gently,
but firmly, press the clean plate over the foil seal.
— If using only part of the plate, use the bottom of a clean eight-tube strip, with
caps attached, to pierce holes in the seals of the wells that will be used for
ligation. Repeat with a new, clean eight-tube strip, with caps attached, for each
row or column of adapters that will be used for ligation.
— Using an eight-tip multichannel pipette, transfer 2.5 µl of the appropriate thawed
RNA Adapter from the RAP well to each well of the ALP plate.
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Ligate Adapters
Date/Time: _______________________________
[_] 7
Operator: _______________________________
Place the ALP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
Stop time: _____________________
[_] 8
Remove and discard 79.5 µl supernatant from each well of the ALP plate.
[_] 9
With the ALP plate on the magnetic stand, add 200 µl freshly prepared 80% EtOH to each
well without disturbing the beads.
[_] 10 Incubate the ALP plate at room temperature for 30 seconds, and then remove and discard all
of the supernatant from each well.
[_] 11 Repeat steps 9 and 10 one time for a total of two 80% EtOH washes.
[_] 12 With the ALP plate on the magnetic stand, let the samples air-dry at room temperature for
15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 13 Remove the ALP plate from the magnetic stand.
[_] 14 Add 52.5 µl Resuspension Buffer to each well of the ALP plate. Mix thoroughly as follows:
[_] a Seal the ALP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the ALP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 15 Incubate the ALP plate at room temperature for 2 minutes.
Start time: _____________________
Stop time: _____________________
[_] 16 Centrifuge the ALP plate to 280 × g for 1 minute.
[_] 17 Remove the adhesive seal from the ALP plate.
[_] 18 Place the ALP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
Stop time: _____________________
[_] 19 Transfer 50 µl supernatant from each well of the ALP plate to the corresponding well of the
new MIDI plate labeled with the CAP barcode.
[_] 20 Vortex the AMPure XP Beads until they are well dispersed.
[_] 21 Add 50 µl of mixed AMPure XP Beads to each well of the CAP plate for a second cleanup.
Mix thoroughly as follows:
[_] a Seal the CAP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CAP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 22 Incubate the CAP plate at room temperature for 15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 23 Centrifuge the CAP plate to 280 × g for 1 minute.
[_] 24 Remove the adhesive seal from the CAP plate.
[_] 25 Place the CAP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
Stop time: _____________________
[_] 26 Remove and discard 95 µl supernatant from each well of the CAP plate.
Page 20 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
[_] 28 Incubate the CAP plate at room temperature for 30 seconds, and then remove and discard all
of the supernatant from each well.
[_] 29 Repeat steps 27 and 28 one time for a total of two 80% EtOH washes.
[_] 30 With the CAP plate on the magnetic stand, let the samples air-dry at room temperature for
15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 31 Remove the CAP plate from the magnetic stand.
[_] 32 Add 22.5 µl Resuspension Buffer to each well of the CAP plate. Mix thoroughly as follows:
[_] a Seal the CAP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CAP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 33 Incubate the CAP plate at room temperature for 2 minutes.
Start time: _____________________
Stop time: _____________________
[_] 34 Centrifuge the CAP plate to 280 × g for 1 minute.
[_] 35 Remove the adhesive seal from the CAP plate.
[_] 36 Place the CAP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
Stop time: _____________________
[_] 37 Transfer 20 µl supernatant from each well of the CAP plate to the corresponding well of the
new HSP plate labeled with the PCR barcode.
SAFE STOPPING POINT
If you do not plan to proceed immediately to Enrich DNA Fragments on page 23, you can safely
stop the protocol here. If you are stopping, seal the PCR plate with a Microseal ‘B’ adhesive seal
and store at -15°C to -25°C for up to seven days.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Part # 15031057 Rev. E
Page 21 of 32
Ligate Adapters
[_] 27 With the CAP plate on the magnetic stand, add 200 µl freshly prepared 80% EtOH to each
well.
TruSeq Stranded mRNA Sample Prep HS Protocol
Ligate Adapters
Experienced User Card and Lab Tracking Form
Page 22 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process uses PCR to selectively enrich those DNA fragments that have adapter molecules
on both ends and to amplify the amount of DNA in the library. The PCR is performed with a
PCR Primer Cocktail that anneals to the ends of the adapters. Minimize the number of PCR
cycles to avoid skewing the representation of the library.
Consumables
Item
Quantity
Storage
Supplied By
PCR Master Mix (PMM)
1 tube per 48 reactions
-15°C to -25°C
Illumina
PCR Primer Cocktail (PPC)
1 tube per 48 reactions
-15°C to -25°C
Illumina
Resuspension Buffer (RSB)
1 tube
2°C to 8°C
Illumina
Barcode labels for:
• CPP (Clean Up PCR Plate)
barcode label
• TSP1 (Target Sample Plate)
barcode label
1 label per plate
15°C to 30°C
Illumina
96-well HSP Plate
1
15°C to 30°C
User
96-well MIDI Plate
1
15°C to 30°C
User
AMPure XP Beads
50 µl per sample
2°C to 8°C
User
Freshly Prepared 80% Ethanol
(EtOH)
400 µl per sample
15°C to 30°C
User
Microseal ‘A’ Film
1
15°C to 30°C
User
Microseal ‘B’ Adhesive Seals
3
15°C to 30°C
User
RNase/DNase-free Eight-Tube
Strips and Caps
(if using multichannel pipettes)
5
15°C to 30°C
User
RNase/DNase-free Reagent
Reservoirs
(if using multichannel pipettes)
5
15°C to 30°C
User
Make PCR
[_] 1
Add 5 µl of thawed PCR Primer Cocktail to each well of the PCR plate.
[_] 2 Add 25 µl of thawed PCR Master Mix to each well of the PCR plate.
[_] a Seal the PCR plate with a Microseal ‘A’ film.
[_] b Shake the PCR plate on a microplate shaker at 1600 rpm for 20 seconds.
[_] 3
Centrifuge the PCR plate to 280 × g for 1 minute.
Part # 15031057 Rev. E
Page 23 of 32
Enrich DNA Fragments
Enrich DNA Fragments
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Enrich DNA Fragments
Date/Time: _______________________________
Operator: _______________________________
Amp PCR
[_] 1
Place the sealed PCR plate on the pre-programmed thermal cycler. Close the lid, then select
and run PCR to amplify the plate.
[_] a Choose the pre-heat lid option and set to 100°C
[_] b 98°C for 30 seconds
[_] c 15 cycles of:
— 98°C for 10 seconds
— 60°C for 30 seconds
— 72°C for 30 seconds
[_] d 72°C for 5 minutes
[_] e Hold at 4°C
Clean Up PCR
[_] 1
Remove the adhesive seal from the PCR plate.
[_] 2
Vortex the AMPure XP Beads until they are well dispersed.
[_] 3
Do one of the following, depending on the adapter type used:
• If using the RNA Adapter tubes, add 50 µl of the mixed AMPure XP Beads to each well
of the new MIDI plate labeled with the CPP barcode.
• If using the RAP, add 47.5 µl of the mixed AMPure XP Beads to each well of the new
MIDI plate labeled with the CPP barcode.
[_] 4
Transfer the entire contents from each well of the PCR plate to the corresponding well of the
CPP plate containing 50 µl of mixed AMPure XP Beads. Mix thoroughly as follows:
[_] a Seal the CPP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CPP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 5
Incubate the CPP plate at room temperature for 15 minutes.
Start time: _____________________
Stop time: _____________________
[_] 6
Centrifuge the CPP plate to 280 × g for 1 minute.
[_] 7
Remove the adhesive seal from the CPP plate.
[_] 8
Place the CPP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
[_] 9
Stop time: _____________________
Remove and discard 95 µl supernatant from each well of the CPP plate.
[_] 10 With the CPP plate on the magnetic stand, add 200 µl freshly prepared 80% EtOH to each
well without disturbing the beads.
[_] 11 Incubate the CPP plate at room temperature for 30 seconds, and then remove and discard all
of the supernatant from each well.
[_] 12 Repeat steps 10 and 11 one time for a total of two 80% EtOH washes.
[_] 13 With the CPP plate on the magnetic stand, let the samples air-dry at room temperature for
15 minutes, and then remove the plate from the magnetic stand.
Start time: _____________________
Stop time: _____________________
Page 24 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
[_] 15 Incubate the CPP plate at room temperature for 2 minutes.
Start time: _____________________
Stop time: _____________________
[_] 16 Centrifuge the CPP plate to 280 × g for 1 minute.
[_] 17 Remove the adhesive seal from the CPP plate.
[_] 18 Place the CPP plate on the magnetic stand at room temperature for 5 minutes or until the
liquid is clear.
Start time: _____________________
Stop time: _____________________
[_] 19 Transfer 30 µl supernatant from each well of the CPP plate to the corresponding well of the
new HSP plate labeled with the TSP1 barcode.
SAFE STOPPING POINT
If you do not plan to proceed immediately to Validate Library on page 27, you can safely stop the
protocol here. If you are stopping, seal the TSP1 plate with a Microseal ‘B’ adhesive seal and store
at -15°C to -25°C for up to 7 days.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Part # 15031057 Rev. E
Page 25 of 32
Enrich DNA Fragments
[_] 14 Add 32.5 µl Resuspension Buffer to each well of the CPP plate. Mix thoroughly as follows:
[_] a Seal the CPP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the CPP plate on a microplate shaker at 1800 rpm for 2 minutes.
TruSeq Stranded mRNA Sample Prep HS Protocol
Enrich DNA Fragments
Experienced User Card and Lab Tracking Form
Page 26 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
Illumina recommends performing the following procedures for quality control analysis on your
sample library and quantification of the DNA library templates.
Quantify Libraries
To achieve the highest quality data on Illumina sequencing platforms, it is important to create
optimum cluster densities across every lane of the flow cell. Optimizing cluster densities requires
accurate quantitation of DNA library templates. Quantify your libraries using qPCR according to
the Illumina Sequencing Library qPCR Quantification Guide (part # 11322363).
Quality Control
[_] 1
Load 1 µl of the resuspended construct on an Agilent Technologies 2100 Bioanalyzer using a
DNA-specific chip such as the Agilent DNA 1000.
[_] 2
Check the size and purity of the sample. The final product should be a band at
approximately 260 bp.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Part # 15031057 Rev. E
Page 27 of 32
Validate Library
Validate Library
TruSeq Stranded mRNA Sample Prep HS Protocol
Validate Library
Experienced User Card and Lab Tracking Form
Page 28 of 32
Part # 15031057 Rev. E
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Date/Time: _______________________________
Operator: _______________________________
This process describes how to prepare DNA templates for cluster generation. Indexed DNA
libraries are normalized to 10 nM in the DCT plate and then pooled in equal volumes in the
PDP plate. DNA libraries not intended for pooling are normalized to 10 nM in the DCT plate.
Consumables
Item
Quantity
Storage
Supplied By
Barcode labels for:
• DCT (Diluted Cluster Template)
• PDP (Pooled DCT Plate)
(for pooling only)
1 label per plate
15°C to 30°C
Illumina
96-well HSP Plate
(for pooling only)
1
15°C to 30°C
User
96-well MIDI Plate
1
15°C to 30°C
User
Microseal ‘B’ Adhesive Seals
5
15°C to 30°C
User
Tris-HCl 10 mM, pH8.5 with
0.1% Tween 20
Enough to normalize
the concentration of
each sample library to
10 nM
15°C to 30°C
User
Make DCT
[_] 1
Transfer 10 µl of sample library from each well of the TSP1 plate to the corresponding well
of the new MIDI plate labeled with the DCT barcode.
[_] 2
Normalize the concentration of sample library in each well of the DCT plate to 10 nM using
Tris-HCl 10 mM, pH 8.5 with 0.1% Tween 20.
[_] 3 Mix the DCT plate as follows:
[_] a Seal the DCT plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the DCT plate on a microplate shaker at 1000 rpm for 2 minutes.
[_] 4
Centrifuge the DCT plate to 280 × g for 1 minute.
[_] 5
Remove the adhesive seal from the DCT plate.
[_] 6
Depending on the type of library you want to generate, do one of the following:
• For non-pooled libraries, the protocol stops here. Do one of the following:
— Proceed to cluster generation.
— Seal the DCT plate with a Microseal ‘B’ adhesive seal and store at -15°C to -25°C.
• For pooled libraries, proceed to Make PDP (for pooling only).
Make PDP (for pooling only)
[_] 1
Determine the number of samples to be combined together for each pool.
Part # 15031057 Rev. E
Page 29 of 32
Normalize and Pool Libraries
Normalize and Pool Libraries
TruSeq Stranded mRNA Sample Prep HS Protocol
Experienced User Card and Lab Tracking Form
Normalize and Pool Libraries
Date/Time: _______________________________
[_] 2
Operator: _______________________________
Do one of the following:
• If pooling 2–24 samples:
— Transfer 10 µl of each normalized sample library to be pooled from the DCT plate to
one well of the new HSP plate labeled with the PDP barcode.
— The total volume in each well of the PDP plate should be 10X the number of
combined sample libraries and 20–240 µl (2–24 libraries).
• If pooling 25–96 samples:
— Using a multichannel pipette, transfer 5 µl of each normalized sample library in
column 1 from the DCT plate to column 1 of the new HSP plate labeled with the
PDP barcode.
— Transfer 5 µl of each normalized sample library in column 2 from the DCT plate to
column 1 of the PDP plate.
— Repeat the transfer for as many times as there are remaining columns in the DCT
plate. The result is a PDP plate with pooled samples in column 1. Mix the PDP plate
as follows:
— Seal the PDP plate with a Microseal ‘B’ adhesive seal.
— Shake the PDP plate on a microplate shaker at 1800 rpm for 2 minutes.
— Centrifuge the PDP plate to 280 × g for 1 minute.
— Remove the adhesive seal from the PDP plate.
— Combine the contents of each well of column 1 into well A2 of the PDP plate for the
final pool.
[_] 3 Mix the PDP plate as follows:
[_] a Seal the PDP plate with a Microseal ‘B’ adhesive seal.
[_] b Shake the PDP plate on a microplate shaker at 1800 rpm for 2 minutes.
[_] 4
Centrifuge the PDP plate to 280 × g for 1 minute.
[_] 5
Do one of the following:
• Proceed to cluster generation.
• Store the sealed PDP plate at -15°C to -25°C.
Comments
__________________________________________________________________________________
__________________________________________________________________________________
Page 30 of 32
Part # 15031057 Rev. E
Technical Assistance
For technical assistance, contact Illumina Technical Support.
Table 1 Illumina General Contact Information
Illumina Website
Email
www.illumina.com
[email protected]
Table 2 Illumina Customer Support Telephone Numbers
Region
Contact Number
Region
North America
1.800.809.4566
Italy
Austria
0800.296575
Netherlands
Belgium
0800.81102
Norway
Denmark
80882346
Spain
Finland
0800.918363
Sweden
France
0800.911850
Switzerland
Germany
0800.180.8994
United Kingdom
Ireland
1.800.812949
Other countries
Contact Number
800.874909
0800.0223859
800.16836
900.812168
020790181
0800.563118
0800.917.0041
+44.1799.534000
MSDSs
Material safety data sheets (MSDSs) are available on the Illumina website at
www.illumina.com/msds.
Product Documentation
Product documentation in PDF is available for download from the Illumina website. Go to
www.illumina.com/support, select a product, then click Documentation & Literature.
Part # 15031057 Rev. E
Page 31 of 32
*12345678*
Part # 15031057 Rev. E
Illumina
San Diego, California 92122 U.S.A.
+1.800.809.ILMN (4566)
+1.858.202.4566 (outside North America)
[email protected]
www.illumina.com
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