NudC Pyrophosphatase
cloned at NEB recombinant neb31 37 65 Heat

We are excited to announce that we are in the process of switching all reaction buffers to be BSA-free. Beginning April 2021, we will be gradually transitioning to buffers containing Recombinant Albumin (rAlbumin) for restriction enzymes and some DNA modifying enzymes. All information on the website has been updated to reflect this change. Find more details at www.neb.com/BSA-free.

  • Decaps RNA that contains ADP-containing, non-canonical initiating nucleotides (including NAD+/NADH caps), resulting in ligatible monophosphate at the 5′ end.
  • Hydrolyzes NADH and NAD+ into AMP and reduced nicotinamide monophosphate nucleoside (NMNH), and AMP and nicotinamide monophosphate nucleoside (NMN+), respectively.
  • Hydrolyzes diphosphate dinucleotides and metabolic co-factors containing an ADP moiety such as AppA, FAD, Coenzyme A, etc.
  • Useful for NAD+ decapping or deNADding when NAD+ is the 5′ initiating nucleotide of RNA.
  • Useful for detection and identification of RNA containing non-canonical initiating nucleotides using ligation-based methods such as 5′ RACE and RNA-seq.

This is an Enzyme for Innovation (EFI). EFI is a project initiated by NEB to provide unique enzymes to the scientific community in the hopes of enabling the discovery of new and innovative applications. These enzymes have interesting properties and unique specificities.

 
Catalog # Concentration Size
M0607S 10 µM 250 pmol
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