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cDNA-PCR Barcoding Kit V14
SQK-PCB114.24

A sequencing kit optimised for identification and quantification of full-length transcripts with highest output, including barcodes for up to 24 samples.

This is an Early Access product.

Product lead time: 2 weeks

This kit uses our latest Kit 14 chemistry.

2Early Access
  • Access the latest products from Oxford Nanopore Technologies
  • Provide feedback into the innovation team as the product develops
  • Product Warranty may initially be limited to 1 month as it is so new
  • Product routinely iterates as new features and capabilities are added
  • Estimated lead time in store
  • Product subject to availability

Information

This kit is recommended for users who:

  • Have a limited amount of input material
  • Wish to multiplex samples to reduce price per sample
  • Want to optimise their sequencing experiment for output
  • Would like to identify and quantify full-length transcripts
  • Are interested in differential gene expression
  • Want to characterise and quantify isoforms, splice variants, and fusion transcripts

This is an Early Access product. For more information about our Early Access programmes, please see this article on product release phases.

Please note that to use this kit, you will need to purchase additional 3rd party reagents: see the "3rd party materials" tab for more detail.

The cDNA-PCR Barcoding Kit 24 V14 features:

| Feature | Property | | ---------- | ---------- | | Preparation time | ~350 minutes | | Input requirement | 10 ng poly(A)+ RNA or 500 ng total RNA | | RT Required | Yes | | PCR Required | Yes | | Read length | Enriched for full-length cDNA during PCR | | Kit chemistry | Kit 14 | | Associated protocols | Please refer to the Protocols tab. | | Multiplexing options | • cDNA-PCR Barcoding Kit 24 V14 • Flow Cell Wash Kit | | Pack size | 6 reactions | | Storage | -20°C to -30°C | | Stability | This kit is stable during shipping for 7 days at temperatures up to 25ºC. Upon receipt, please store the kit at -20°C to -30°C.
Oxford Nanopore Technologies deem the useful life of the product to be 3 months from receipt by the customer. |

Barcoding or multiplexing is useful when the amount of data required per sample is less than the total amount of data that can be generated from a single flow cell. It allows a user to pool multiple samples and sequence them together, making more efficient use of the flow cell.

Multiplexing samples onto one flow cell can reduce the cost per sample for a user.

The cDNA-PCR Barcoding Kit is used to prepare cDNA for nanopore sequencing for up to 24 samples, from an input of as low as 10 ng polyadenylated RNA. Users who do not have polyadenylated enriched RNA can use 500 ng of total RNA but additional optimisation may be required.

The protocol uses a strand switching method to select for full length transcripts, allowing the identification of splice variants, with the incorporation of unique molecular identifiers (UMI) during this step. Taking full-length polyadenylated RNA, complementary strand synthesis and strand switching are performed using kit-supplied oligonucleotides. The kit contains 24 primer pairs which are used to generate and then amplify double-stranded cDNA by PCR amplification using primers that contain 5’ tags and facilitate the ligase-free attachment of Rapid Sequencing Adapters. Amplified and barcoded samples are then pooled together and the Rapid Sequencing Adapters are added to the pooled mix.

The cDNA-PCR Sequencing Kit also includes a cDNA RT adapter and RT primer to prime cDNA synthesis from the end of a transcript to reduce overlaps during the reverse transcription step and to allow users to measure poly(A)+ tail lengths. Additionally, a new post-PCR wash step further reduces short artifacts that are observed when using low-quality samples.

Shipping and logistics:

Flow cells and kits are shipped together in an environmentally friendly temperature-controlled shipping box.

Products are shipped to customers within the USA and EU Monday to Thursday. Shipments to Canada, Norway, Korea and Japan are expedited Monday to Wednesday; with Australia and New Zealand leaving our warehouses on a Friday. Shipments to the rest of the world are made on Mondays to allow the full working week for packages to arrive.

The delivery charges are calculated when a quote is raised or during checkout. Once an order is made, the delivery ID and delivery information can be tracked in the Store.

Workflow

Taking full-length polyadenylated RNA, complementary strand synthesis and strand switching are performed using kit-supplied oligonucleotides. The kit contains 24 primer pairs that are used to generate and then amplify double-stranded cDNA by PCR amplification using rapid attachment barcode primers. These primers contain 5’ tags and facilitate the ligase-free attachment of Rapid Sequencing Adapters. Amplified and barcoded samples are then pooled together and Rapid Sequencing Adapters are added to the pooled mix.

pcb114-24 workflow update june2025

What's in the box

The cDNA-PCR Barcoding Kit 24 V14 (SQK-PCB114.24) contains 24 unique barcodes and enough reagents for 6 reactions.

SQK PCB114.24 Plated Kit content june2025

NameAcronymCap colourNo. of vialsFill volume per vial (μl)
Strand Switching Primer IISSPIIViolet1350
RT PrimerRTPYellow1200
cDNA RT AdapterCRTAAmber1200
Annealing BufferABOrange1200
Rapid AdapterRAGreen115
Adapter Buffer ADB  Clear   100 
Elution BufferEBBlack2500
Short Fragment BufferSFBClear313,000
Sequencing BufferSBRed1700
Library BeadsLIBPink1600
Library SolutionLISWhite cap, pink label1600
Flow Cell Tether   FCT     Purple    1   200 
Flow Cell Flush   FCF     Clear cap, light blue label    1     15,500  
Barcode Primers 1-24 at 1 µMBP01-24-2 plates, 3 sets of primer barcodes per plate12 µl per well

3rd party materials

Consumables:

  • T3 DNA Ligase (NEB, M0317)
  • Lambda Exonuclease (NEB, M0262L)
  • USER (Uracil-Specific Excision Reagent) Enzyme (NEB, M5505L)
  • 10 mM dNTP solution (e.g. NEB N0447)
  • TaKaRa Ex Premier DNA Polymerase (TaKaRa, RR370A/RR370B)
  • Maxima H Minus Reverse Transcriptase (200 U/µl) with 5x RT Buffer (ThermoFisher, EP0751)
  • RNaseOUT™, 40 U/μl (Life Technologies,10777019)
  • Thermolabile Exonuclease I (NEB, M0568)
  • Agencourt RNAClean XP beads (Beckman Coulter®, A63987)
  • Agencourt AMPure XP beads (Beckman Coulter™, A63881)
  • Nuclease-free water (e.g. Thermo Scientific, AM9937)
  • Bovine Serum Albumin (BSA) (50 mg/ml) (e.g Invitrogen™ UltraPure™ BSA 50 mg/ml, AM2616)
  • Freshly prepared 80% ethanol in nuclease-free water
  • 1.5 ml Eppendorf DNA LoBind tubes
  • 0.2 ml thin-walled PCR tubes
  • Qubit™ dsDNA HS Assay Kit (ThermoFisher, Q32851)
  • Qubit™ RNA HS Assay Kit (ThermoFisher, Q32852)
  • Qubit™ Assay Tubes (Invitrogen, Q32856)

Equipment:

  • Hula mixer (gentle rotator mixer)
  • Magnetic separator, suitable for 1.5 ml Eppendorf tubes
  • Microfuge
  • Vortex mixer
  • Thermal cycler
  • Multichannel pipette
  • P1000 pipette and tips
  • P200 pipette and tips
  • P100 pipette and tips
  • P20 pipette and tips
  • P10 pipette and tips
  • P2 pipette and tips
  • Ice bucket with ice
  • Timer
  • Qubit fluorometer (or equivalent for QC check)
  • Multichannel pipette capable of 20-200 μl

Compatibility

Kits:

  • Rapid Adapter Auxiliary V14 (EXP-RAA114)
  • Sequencing Auxiliary Vials V14 (EXP-AUX003)
  • Sequencing Auxiliary Vials V14 XL (EXP-AUX003-XL)
  • RNA Control Expansion (EXP-RCS001)
  • SFB Expansion (EXP-SFB001)
  • Flow Cell Wash Kit (EXP-WSH004)
  • Flow Cell Wash Kit XL (EXP-WSH004-XL)
  • Flow Cell Priming Kit (EXP-FLP004)
  • Flow Cell Priming Kit XL (EXP-FLP004-XL)

Flow cells:

  • FLO-MIN114
  • FLO-PRO114M

Devices:

  • MinION
  • GridION
  • PromethION