recombinant, E. coli
For in vitro use only!
Unit Definition: One unit is the amount of enzyme required to degrade 1 μg of RNA in 30 minutes at 37 °C.
Shipping: shipped on blue ice
Storage Conditions: store at -20 °C
avoid freeze/thaw cycles
Shelf Life: 12 months
Molecular Weight: 27.0 kDa
Purity: > 95 % (SDS-PAGE)
Form: liquid (Supplied in 10 mM Tris-HCl pH 8.0, 200 mM NaCl and 50 % [v/v] glycerol)
Ribonuclease l (27 kD) is a completely nonspecific ribonuclease that hydrolyzes the phosphodiester bond of all four bases.
It degrades any RNA to a mixture of mono-, di-, and trinucleotides and does not degrade DNA, although it does bind to DNA. It has a marked preference for single-stranded RNA over double-stranded RNA, which allows it to work well in RNase Protection Assays. It has a high specific activity which, coupled with its non-specificity, typically results in complete degradation of RNA using ng amounts of protein.
Contains no endonuclease or exonuclease activity toward DNA substrates.
For RNase Protection Assays using approximately 10 μg of total RNA per sample, we suggest using 100 - 500 units of enzyme at 37 °C for 30 min.
For boiling lysate minipreps we suggest using 50 units at 37 °C for 30 min.
Please click the black arrow on the right to expand the citation list. Click publication title for the full text.
Meador et al. (1990) Cloning and sequencing the gene encoding Escherichia coli ribonuclease I: exact physical mapping using the genome library. Gene 95: 1.
Ono et al. (1987) Nucleotide sequence of the pnd gene in plasmid R483 and role of the pnd gene product in plasmolysis. Mirobiol. Immunol.31:1071.
Ito et al. (1983) The roles of RNA polymerase and RNAase I in stable RNA degradation in Escherichia coli carrying the srnB+gene. Biochim. Biophys. Acta 739: 27.