This unique workflow meets the demand for a highly sensitive, yet robust method that consistently generates high-quality, full-length transcript sequencing data from a single cell or ultra-low input RNA.
Optimized cDNA synthesis and amplification steps incorporate template switching, as well as utilize a unique protocol and suite of reagents. Even low-abundance transcripts are represented in the high yields of cDNA obtained. Subsequent library construction incorporates the Ultra™ II FS enzymatic DNA fragmentation/end repair/dA-tailing mix in a simple and efficient workflow.
NEBNext Single Cell/Low Input RNA Library Prep workflow
- Generate the highest yields of high-quality full-length transcript sequencing libraries from single cells, or as little as 2 pg – 200 ng total RNA
- Experience unmatched detection of low abundance transcripts
- Rely on consistent transcript detection for a wide range of input amounts and sample types
- Obtain full length, uniform transcript coverage, regardless of input amount or sample type
- Use with cultured or primary cells, or total RNA
- Save time with a fast, streamlined workflow, minimal handling steps and hands-on time
- – Single-tube protocol from cell lysis to cDNA
- – Enzymatic DNA fragmentation, end repair and dA-tailing reagents in a single enzyme mix, with a single protocol, regardless of GC content
- Available with or without library construction reagents
Generate higher library yields with the NEBNext Single Cell/Low Input RNA Library Prep Kit
Sequencing libraries were generated from HeLa, Jurkat and M1 single cells or 10 pg of Universal Human Reference (UHR) RNA (Agilent® #740000) with recommended amounts of ERCC RNA Spike-In Mix I (Thermo Fisher Scientific® #4456740). The NEBNext Single Cell/Low Input RNA Library Prep Kit, or the SMART-Seq v4 Ultra® Low Input RNA Kit for Sequencing (Clontech® #634891) plus the Nextera XT DNA Library Prep Kit (Illumina® #FC-131-1096) were used. For the NEBNext workflow ~80% of the cDNA was used as input into sequencing library preparation, and libraries were amplified with 8 PCR cycles. For the SMART-Seq v4/Nextera XT workflow, as recommended, 125 pg of cDNA was used as input in sequencing library preparation and 12 PCR cycles were used for amplification. Error bars indicate standard deviation for 6-11 replicates.
The NEBNext Single Cell/Low Input RNA Library Prep Kit increases transcript detection
Sequencing libraries were generated from Jurkat single cells (6 replicates) using the NEBNext Single Cell/Low Input RNA Library Prep Kit, or the SMART-Seq v4 Ultra® Low Input RNA Kit for Sequencing (Clontech® # 634891) plus the Nextera XT DNA Library Prep Kit (Illumina® #FC-131-1096). Libraries were sequenced on an Illumina NextSeq® 500 using paired-end mode (2×76 bp). TPM = Transcripts per Kilobase Million. Each dot represents the number of transcripts identified at the given TPM range, and each box represents the median, first and third quartiles per replicate. Salmon 0.6 was used for read mapping and quantification of all GENCODE v25 transcripts. Panels show the number of transcripts detected within the following TPM ranges: 1-5, 5-10, 10-50 and >50 TPM. Increased identification of low abundance transcripts is observed with the NEBNext libraries.
The NEBNext Single Cell/Low Input RNA Library Prep Kit provides uniform coverage across the length of transcripts
Sequencing libraries were generated from HeLa, Jurkat and M1 single cells, or 10 pg of Universal Human Reference (UHR) RNA (Agilent® #740000) with recommended amounts of ERCC RNA Spike-In Mix I (Thermo Fisher Scientific® #4456740). The NEBNext Single Cell/Low Input RNA Library Prep Kit, or the SMART-Seq v4 Ultra® Low Input RNA Kit for Sequencing (Clontech® # 634891) plus the Nextera XT DNA Library Prep Kit (Illumina® #FC-131-1096) were used. Libraries were sequenced on an Illumina NextSeq® 500 using paired-end mode (2×76 bp). Gene body coverage shown is an average of four replicates and was calculated using Picard tools. The global view of the 5´ to 3´ coverage of the RefSeq transcripts reveals both consistency across different sample types and uniformity across the transcript length in the NEBNext libraries.
Available products
| PRODUCT | REF. | SIZE | PRICE | MORE INFO |
|---|---|---|---|---|
| NEBNext Single Cell/Low Input RNA Library Prep Kit for Illumina | E6420S | 24 rxns |  |
 |
| E6420L | 96 rxns | |||
| NEBNext Single Cell/ Low Input cDNA Synthesis & Amplification Module | E6421S | 24 rxns | |
|
| E6421L | 96 rxns | |||
| NEBNext Multiplex Oligos for Illumina
(Index Primers Set 1, 2, 3, 4) |
E7335S/L, E7500S/L, E7710S/L, E7730S/L | 24 / 96 rxns | |
|
| NEBNext Multiplex Oligos for Illumina (96 Index Primers) | E6609S | 96 rxns | |
|
| E6609L | 384 rxns | |||
| NEBNext Multiplex Oligos for Illumina (Dual Index Primers Set 1, 2) | E7600S, E7780S | 96 rxns | |
|
| NEBNext Multiplex Oligos for Illumina (96 Unique Dual Index Primer Pairs) | E6440S/L | 96 / 384 rxns | |
|
| NEW NEBNext Magnetic Separation Rack | S1515S | 1 rack pour 24 tubes | |
|
Stand: 19.06.2018
Further information can be found in our Technical Resources section or at neb.com
