SMART-Seq Total RNA Library Prep with ZapR Depletion (with UMIs)

NOTE: The SMART-Seq Total RNA Library Prep with ZapR Depletion (with UMIs) is the updated name of the SMART-Seq Total RNA Pico Input with UMIs (ZapR Mammalian) with the same components, performance, and price.

This kit can now be used for library preparation with higher input amounts—up to 1 µg of total RNA—while maintaining the same exceptional performance. Download our new flyer for the data

SMART-Seq Total RNA Library Prep with ZapR Depletion (with UMIs) is designed for efficient preparation of Illumina sequencing libraries from picogram to microgram input amounts of high-quality, partially degraded, or low-quality total RNA, including total RNA prepared from FFPE or LCM samples. The kit features a streamlined workflow that retains strand information and incorporates indexes and adapters during the reverse-transcription and PCR-amplification steps. The library design featured in this kit adds an 8 nucleotide (nt) unique molecular identifier (UMI) through the reverse-transcription step to mitigate potential PCR bias as well as to provide additional information for transcript quantification, specifically for true variants and rare mutations.

NOTE: The SMART-Seq Total RNA Library Prep with ZapR Depletion (with UMIs) is the updated name for the SMART-Seq Total RNA Pico Input with UMIs (ZapR Mammalian) with the same components, performance, and price.

This kit can now be used for library preparation with higher input amounts—up to 1 µg of total RNA—while maintaining the same exceptional performance. Download our new flyer for the data

SMART-Seq Total RNA Library Prep with ZapR Depletion (with UMIs) is designed for efficient preparation of Illumina sequencing libraries from picogram to microgram input amounts of high-quality, partially degraded, or low-quality total RNA, including total RNA prepared from FFPE or LCM samples. The kit features a streamlined workflow that retains strand information and incorporates indexes and adapters during the reverse transcription and PCR amplification steps. The library design featured in this kit adds an 8 nucleotide (nt) unique molecular identifier (UMI) through the reverse-transcription step to mitigate potential PCR bias as well as to provide additional information for transcript quantification, specifically for true variants and rare mutations.

This kit incorporates our proprietary SMART (Switching Mechanism at the 5’ end of RNA Template) technology and includes refinements to the SMARTer method for stranded RNA-seq that simplify the library preparation workflow and improve sequencing performance. This method was developed to work with either high- or low-quality total RNA, does not require additional rRNA removal methods or kits, and produces sequencing libraries that retain strand-of-origin information. The integrated removal of cDNAs derived from rRNA—typically present in high abundance following cDNA synthesis from total RNA inputs—makes the workflow extremely sensitive, yielding data that is highly reproducible with low mapping to rRNA.

The entire protocol, including library prep and purification, takes only ~6.5 hours.

For your convenience, we have outlined the differences between our total RNA-seq kits below: 

Overview

  • Accommodates a wide input range—start from 250 pg–1 µg of total RNA from human, mouse, or rat
  • Seamless integration of UMIs—accurately identify true variants and rare mutations and mitigate potential PCR amplification bias and sequencing errors
  • Versatile—generate reproducible data from RNA of any quality (including FFPE and LCM samples and cell-free RNA)
  • Fast, streamlined protocol—go from start to finish in ~6.5 hours and save time during library purification with an improved buffer formulation
  • Compatible with Illumina sequencing—generate Illumina-ready libraries with up to 384 combinations of indexes

More Information

Applications

  • Robust NGS library construction that retains strand information
  • RNA-seq on all Illumina platforms
  • Coding and noncoding information from total mammalian RNA of any quality, including RNA obtained from FFPE samples

Additional product information

Please see the product's Certificate of Analysis for information about storage conditions, product components, and technical specifications. Please see the Kit Components List to determine kit components. Certificates of Analysis and Kit Components Lists are located under the Documents tab.