E7850S, NEBNext rRNA Depletion Kit (Bacteria) - 6 rxns

E7850S, NEBNext rRNA Depletion Kit (Bacteria) - 6 rxns

N0558S, TriDye Ultra Low Range DNA Ladder - 125 gel lanes

N0558S, TriDye Ultra Low Range DNA Ladder - 125 gel lanes

M0466S, Template Switching RT Enzyme Mix - 20 rxns

667,59 RON

The Template Switching RT Enzyme Mix and accompanying reaction buffer enable efficient template switching activity in a reverse transcription reaction.

SKU
NEB_M0466S

The Template Switching RT Enzyme Mix and accompanying reaction buffer enable efficient template switching activity in a reverse transcription reaction. The mix contains a unique RT and Murine RNase Inhibitor. Unlike competitor RT products, no additives (such as PEG or betaine) are required for optimal performance, simplifying reaction setup. In conjunction with a template switching oligo (TSO), cDNA is synthesized with a known sequence of choice attached to the 3′ end. The resulting cDNA can be amplified by PCR or serve as template for 5′ RACE (rapid amplification of cDNA ends) or 2nd strand cDNA synthesis.

  • Prepare RNA-seq libraries from extremely low input: single cells/nuclei or 2 pg of total RNA.
  • Perform 5′ RACE from as low as 10 ng total RNA.
  • Low background for RNA-seq or 5′ RACE
  • Enzyme mix contains Murine RNase Inhibitor, no additives necessary
  • Compatible with various template switching oligos (TSOs), RT primers, and DNA polymerases for full length cDNA amplification
  • Enjoy faster protocols as compared to alternative RNA-seq methods (eg. Smart-Seq®)

 

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Price 561,00 RON (preturile sunt fara TVA)
Description

The Template Switching RT Enzyme Mix and accompanying reaction buffer enable efficient template switching activity in a reverse transcription reaction. The mix contains a unique RT and Murine RNase Inhibitor. Unlike competitor RT products, no additives (such as PEG or betaine) are required for optimal performance, simplifying reaction setup. In conjunction with a template switching oligo (TSO), cDNA is synthesized with a known sequence of choice attached to the 3′ end. The resulting cDNA can be amplified by PCR or serve as template for 5′ RACE (rapid amplification of cDNA ends) or 2nd strand cDNA synthesis.

  • Prepare RNA-seq libraries from extremely low input: single cells/nuclei or 2 pg of total RNA.
  • Perform 5′ RACE from as low as 10 ng total RNA.
  • Low background for RNA-seq or 5′ RACE
  • Enzyme mix contains Murine RNase Inhibitor, no additives necessary
  • Compatible with various template switching oligos (TSOs), RT primers, and DNA polymerases for full length cDNA amplification
  • Enjoy faster protocols as compared to alternative RNA-seq methods (eg. Smart-Seq®)