New Channels on Bitesize Bio

To help you find information on exactly what you need we're implementing channels, a new way to browse content

Each channel is focused on a specific technique or area and authored/presented by hand-picked authors who are experts in their field. Make sure you don't miss a thing by checking the box below for each channel that interests you.

In return we'll send you one email per month that brings you the latest from your chosen channel(s), along with free members-only content.

Check out our upcoming new channels; Flow Cytometry and Cell Culture, we'll be launching them very soon!

I would like to receive the newsletters for the following channels

Cell Culture
Flow Cytomery
Microscopy & Imaging
Next Generation Sequencing
Writing, Publishing and Presenting
Cloning & Expression


My email address is:

bleach-pcr

PCR: The Right Way to Decontaminate and Eliminate False Positives

by in PCR & Real-time PCR, Tech Tips
From the Bitesize Bio channel

PCR is highly sensitive, but the downside of that very property is that it makes the technique prone to producing false-positives. In labs where PCR is a staple, like the one I work in, any false-positives are more often than not due to amplicon contamination.

A broken capillary or a PCR plate left carelessly at the table edge is all it takes to aerosolize those amplicons. The next thing you know is it shows up in every PCR reaction that you run.  If you frequently run PCR, then you know what I am talking about.

So what do you do to decontaminate?

Well a simple, but effective way to combat an amplicon contamageddon, is to wipe down everything, equipment, workstations and pipettes, with bleach. Yes, bleach… not HCl. If you routinely use HCl for decontaminating rogue DNA then you definitely need to read on.

Sodium hypochlorite, the active ingredient in bleach, was shown in a 1992 study to effectively protect against amplicon contamination by causing extensive nicking, which prevented the 600bp fragment they tested from being amplified by PCR (see A. M. Prince, L. Andrus PCR: Biotechniques 1992 Mar;12(3):358-60).

The same study showed that even a after 5 minute exposure to 2N HCl, that same 600bp fragment could be detected by PCR. So HCl is not up to the job… its time to get the bleach out.

Which bleach should you use?

The efficacy of bleach in DNA decontamination (and as a disinfectant) depends on the amount of free and available chlorine. 0.05 – 0.5% of free and available chlorine is considered an intermediate level disinfectant and a commercial bleach (like Clorox) contains 5.84% available chlorine so a 10-100x dilution from a commercial stock will work just fine.

I tend to use a 10 dilution of Clorox and, in the above-mentioned study, Prince and Andrus used around a 20x dilution. You can make your own choice.

How and when to decontaminate

Generously spray workstations/equipment/pipettes with 10% bleach, then let it sit for 15-30 minutes (coffee break time!). Then wipe up the bleach and follow up with a water rinse and wipe — bleach is corrosive, so it will damage materials if residue is not removed by rinsing with water.

This procedure should be carried our before and after each PCR, and definitely after a spill. I religiously stick to a weekly cleaning routine of all of my PCR equipment and workspace and that has gone a long way to preventing amplicon contamination

Important points about diluting and storing bleach

Use clean water to dilute the bleach

I use regular tap water and that has worked well so far but hypochlorites are very unstable and decompose very quickly with hard water, reducing the availability of chlorine. So you may want to use a purer water, just to make sure.

Make fresh dilutions as often as possible

Potency of bleach will reduce over time so, it is essential to regularly make fresh dilutions. If you do not smell the chlorine in the bleach, then it is time to make a fresh dilution. We keep our (1:10) dilutions for about 1-2 weeks.

Store dilutions at room temperature in opaque containers

We use regular plastic spray bottles for the dilutions and store them under the sink. Temperature, light and oxygen are all catalysts for decomposition of bleach.

Make sure you use the correct PPE when handling bleach

Lab coat, gloves and safety glasses…. But you do that anyway, right?

Articles in your inbox

Enter your email to be informed when we publish more articles like this on BsB, and also get access to all of these goodies:

  • Free ebooks and audiobooks on the topics that matter to you
  • Access to Member’s-only articles and Videos
  • Advance notice of new webinars and eBooks
  • Access to make comments and ask questions on BsB



What to read next

qPCR: Plexor and SYBR compared

In my last article I introduced you to the Plexor System. And from that we already know that while in reactions that user SYBR Green for detection, fluorescence increases with accumulation of PCR product, with Plexor the fluoresence decreases. Today I want to compare some other well-known features of SYBR Green chemistry and see how [...]

A new use for acupuncture in qPCR

What do you get when you cross eastern medicine with molecular biology? How about a novel way to isolate mRNA from living cells using acupuncture? That’s just one of many projects going on in Dr. Karl Hasenstein’s lab at the University of Louisiana, Lafayette. Original research performed by Dr. Hasenstein’s lab and presented at the CHI [...]

Mind Your P’s And Q’s: A Short Primer On Proofreading Polymerases

For applications such as site-directed mutagenesis, it is often recommended that you use a proofreading polymerase (also known as high-fidelity polymerases) to minimize the risk of introducing unintended point mutations.  But what is a proofreading polymerase?  What makes them different from other polymerases?  And when should you use them?  Read on to learn more… What [...]

Do Your RT-qPCRs Make The Grade?

Real-time PCR is a technique that is now commonly employed in almost all molecular biology laboratories to quickly answer very specific questions. Northern and Southern blotting are now a thing of the past. No longer do we wait days to know whether a gene is expressed. We can have the answer in 45 minutes! But with the [...]

About the author

What do you think?

8 comments

    • from on

      Peter, good catch! Thanks for pointing that. I have fixed it now :)

  1. from MAD scientist on

    Also, barrier tips help prevent cross contamination. A bit more money but worth it.

  2. from John Mackay on

    Good stuff Shoba. I wouldn’t let chlorine sit on workstations’ stainless steel though. . we spray, wipe and then follow with 70% ethanol to avoid any chlorine pitting issues. But yes, we wipe it on benches and leave it before the 70% wipe.
    One of the issues for us is the actual DNAcidal (?) stability – as you say, its not that stable and I know others use 3% H2O2 which *is* more stable. Would be interesting to know how long it *does* nuke the DNA.

    Best example of the joys of contamination is the intro to the often-cited Kowk and Higuchi paper. Dropping your 100ul reaction (well this was about 1990!) into an Olympic size swimming pool (I add – maybe swimming around a bit to mix it) and then taking out your 100ul again. . .you’d have about 400 templates for contamination (memory disclaimer applies!)

Subscribe to Channels

To receive information about any of our new channels click on the button below.
subscribe to the channel newsletter »

Write for us

Have a short tip, a written
article or a video you'd like
to see published?
write for us »