Promega Corporation

RNasin® Ribonuclease Inhibitor

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7 out of 10 lab stocks may be contaminated

RNase Contamination Happens–Even When You Are Careful

Maintaining RNA integrity is crucial to the success of your experiments. RNase contamination can happen during RNA purification and during routine downstream handling.

Gel analysis of RNA integrity

Nine laboratory buffers and water stocks from an RNA-free zone of an academic lab were tested for RNases. Samples were divided into two aliquots and each was incubated overnight at 37°C with or without RNasin Inhibitor. Seven of the nine stocks contained RNases ( Panel A). Addition of RNasin Inhibitor protected the RNA from degradation ( Panel B).

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50% more protection

Not all RNase Inhibitors are Equal

Some RNase inhibitors offer less than half the protection of Promega RNasin® Inhibitor.

comparison of RNasin with RNaseOUT inhibitors during qRT-PCR

Comparison of RNasin® Ribonuclease Inhibitor and RNaseOUT™ inhibition of RNase A during qRT-PCR. RNA was reverse transcribed and amplified in the presence of RNase A and either Promega RNasin® or a competing RNase inhibitor (RNaseOUT™). Promega RNasin® Inhibitor provided better RNA protection in the presence of RNase.

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A million skin cells are shed per day

Lower Your Risk

Use These Tips to Help You Avoid RNase Contamination

  1. Wear gloves and use sterile technique when handling RNA or reagents that will be used with RNA.

    The most common sources of RNase contamination are hands and bacteria or mold that could be lurking on dust particles or on glassware.

  2. Use sterile, disposable plasticware.

    These products are typically RNase-free and don’t require treatment to inactivate RNases.

  3. Treat non-disposable glassware and plasticware before you use it. For glassware, bake it at 250°C overnight.

    For plasticware, rinse it with 0.1N NaOH/1mM EDTA and then with diethyl pyrocarbonate (DEPC)-treated water.

  4. Reserve a set of chemicals and solutions needed for RNA isolation and analysis as “RNA Only” and keep them separate from reagents for other applications.

    Wear gloves whenever you handle these reagents, and use sterile labware to measure them.

  5. Beware! Autoclaving alone is not sufficient to inactivate all RNases.

    Solutions that you prepare in the lab should be treated by adding DEPC to 0.05% and incubated overnight. Autoclaving the treated solutions for 30 minutes will remove any trace of the DEPC from the solution.

  6. Establish an “RNA Only Work Zone” in your lab that has dedicated equipment, reagents, labware, etc.
  7. Use RNasin® Ribonuclease Inhibitor to help prevent RNA degradation.
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Promega RNasin® is Available in Catalog, Bulk or Custom Sizes

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