Applications - DNA digestion of all types of DNA
- RNA digestion of all types of RNA
- Enzymatic and other heat-labile reactions
SourcePurified from E. coli
Purity- Protease activity is less than the detection limit.
- E. coli genomic DNA contamination is less than the detection limit.
Storage–20°C
BufferSupplied in a buffer [20 mM NaCl, 10 mM Tris-HCl (pH 7.5), 50% glycerol, 2mM MgCl 2]
References1. Yang, H. et al. (2012) J. Virol. 86(23):13122-13123. 2. Baldermann, S. et al. (2010) J. Exp. Bot. 61(11):2967-2977.
Unit Definition One unit is defined as the amount of enzyme required to increase 260 nm absorbance by 0.001 per minute at 37°C and pH 7.5 using salmon sperm DNA as the substrate.
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