Nuclease/Nuc A DuoSet ELISA, 5 Plate Summary
| Source |
N/A |
| Assay Type |
Solid Phase Sandwich ELISA |
| Inter-Assay |
|
| Intra-Assay |
|
| Spike Recovery |
|
| Sample Volume |
|
Applications/Dilutions
| Dilutions |
|
| Application Notes |
No significant interference observed with available related molecules. |
Packaging, Storage & Formulations
| Storage |
Store the unopened product at 2 - 8 °C. Do not use past expiration date. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Nuclease/Nuc A DuoSet ELISA, 5 Plate
Background
Serratia
marcescens endonuclease, is a non-specific nuclease that degrades both
single- and double-stranded nucleic acids, including DNA and RNA, but exhibits no
proteolytic activity (1); therefore, it is ideal for the removal of nucleic acid
contaminants from protein samples and applications where complete digestion of
nucleic acids is desirable. NucA is also commonly used in bioprocessing applications to reduce viscosity of samples caused by genomic DNA. The optimum pH for enzyme activity is found to be
8.0-9.2. It hydrolyzes internal phosphodiester bonds between nucleotides in
nucleic acids to produce 5'-monophosphate oligonucleotides of 3-8 bases in
length (2). The active enzyme is a homodimer with two disulfide bonds in
each monomer that are crucial to the enzyme activity and stability (3). The absolute
activity of the recombinant enzyme is measured by a phosphatase coupled assay (4),
where the 5'-phosphate of oligosaccharides generated by the enzyme is further released
by non-specific alkaline phosphatase and quantitated by Malachite reagents (5).
Benzonase is a registered trademark of Merck KGaA Corp.
-
Benedik, MJ and Strych, U. (1998) FEMS Microbiol Lett. 165:1.
- Nestle, M, et al. (1999) J. Biol. Chem. 274:825.
- Ball, T.K. et al. (1992) Nucleic Acids Res. 20:4971.
- Wu, Z.L. et al. (2011) Glycobiology 21:727.
- Van Veldhoven, P.P. and G.P. Mannaerts (1987) Anal. Biochem. 161:45.
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