Terminator 5'-Phosphate-Dependent Exonuclease
Product Details
ShowThe Terminator 5'-Phosphate Dependent Exonuclease include this enzyme and the 10X Terminator Reaction Buffers A and B.
Terminator 5'-Phosphate-Dependent Exonuclease
Key features
Show- Specific: Processively digests RNA with 5´-monophosphate ends but not RNAs with 5´-triphosphate, 5´-cap or 5´-hydroxyl groups starting from the 5´ end
- Flexible: Use this enzyme to help characterise 5´-ends of RNA and to enrich for mRNA in prokaryotic or eukaryotic total RNA preparations
Size: 40 units
Product information
Terminator™ 5´-Phosphate-Dependent Exonuclease* is a processive 5´ to ;3´ exonuclease that digests RNA that has a 5´-monophosphate end. It does not digest RNA that has a 5´-triphosphate, 5´-cap or 5´-hydroxyl group. Terminator Exonuclease is not inhibited by proteinaceous RNase inhibitors, such as RiboGuard™ RNase Inhibitor or placental ribonuclease inhibitors.
Applications
- Characterise the 5´ termini of RNA transcripts.
- Enrich for mRNA in prokaryotic or eukaryotic total RNA preparations (Figure. 1).
Note: Terminator™ 5´-Phosphate-Dependent Exonuclease has not been optimised for RNA-Sea applications.
![](https://cdn.media.amplience.net/i/biosearchtech/Epicentre-i_terminator_exonucleasereaction.gif?sfvrsn=0.3028050623391365)
Figure 1. A 1-hour Terminator™ Exonuclease reaction digests the large rRNAs in a eukaryotic or prokaryotic total RNA sample, producing an enriched mRNA preparation.
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Figure 2. Normal rat kidney (NRK) total RNA before (A) and after (B) Terminator™ Exonuclease treatment. The Terminator Exonuclease-treated RNA was concentrated 10-fold. | Figure 3. Denaturing agarose gel analysis of E. coli total RNA before (-) and after (+) Terminator™ Exonuclease digestion. The Terminator Exonuclease-treated RNA was concentrated 10-fold. |
![](https://cdn.media.amplience.net/i/biosearchtech/Epicentre-terminator_overview.gif?sfvrsn=0.9849656756669292)
Figure 4. (click to enlarge) Over
Unit Definition: One unit of Terminator™ Exonuclease digests 1 µg of rRNA substrate to acid-soluble nucleotides in 60 minutes at 30 °C under standard assay conditions.
Storage Buffer: 50% glycerol containing 0.05 M Tris-HCl (pH 7.5), 100 mM NaCl, 0.1 mM EDTA, 1 mM DTT, and 0.1% Triton™ X-100.
SDS
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