Ethidium bromide volatile in hot agarose solution?

  • Thread starter Thread starter Monique
  • Start date Start date
  • Tags Tags
    Hot
AI Thread Summary
The discussion centers on the volatility of ethidium bromide (EtBr) when added to hot agarose solutions, raising concerns about potential health hazards for those working with it. Participants express discomfort with the practice of remelting agarose gels containing EtBr, questioning whether it poses a real danger due to possible vapor release. There is a request for information regarding the boiling point and vapor pressure of EtBr to assess its volatility. Additionally, an alternative reagent, Megafluor, is mentioned as a less toxic option for DNA labeling, which does not penetrate cellular membranes and is environmentally friendly, suggesting it could be a safer substitute for EtBr in molecular biology applications.
Monique
Staff Emeritus
Science Advisor
Gold Member
Messages
4,211
Reaction score
68
Is ethidium bromide volatile in hot agarose solution? Some people add ethidium bromide to melted agarose solution, or reuse agarose containing ethidium bromide by melting it. If EtBr is heat-volatile, then it may pose danger to these persons. I always feel uncomfortable when remelting gels and avoid breathing in the air.. is there a real health hazard here?
 
Biology news on Phys.org
Interesting, someone is on the same wavelength as me.. posted one day in advance..

Does anyone know the boiling point and vapour pressure of EtBR?
 
Originally posted by iansmith
check this link out

http://micro.nwfsc.noaa.gov/forums/viewtopic.php?t=1524
Tnanks so much for bringing that Forum to my attention Ian. That might really help me over the next couple of years as I start getting into the really technical side of Molecular Biology =)
 
Last edited by a moderator:
You're welcome

I have check this forum for a while but never used any of the information given. The guy that works with me has a good background in biotechnology and molecular biology but the forum migth be usefull later.
 
There is another reagent for DNA labelling (I have never used it), its name is megafluor (EuroClone) and the toxicity is less than the EtBr, is not able to pass through cellular membranes and does not produce environmental pollution. It uses the standard electrophoretic techniques and transilluminators.
An alternative!
 
https://www.nhs.uk/mental-health/conditions/body-dysmorphia/ Most people have some mild apprehension about their body, such as one thinks their nose is too big, hair too straight or curvy. At the extreme, cases such as this, are difficult to completely understand. https://www.msn.com/en-ca/health/other/why-would-someone-want-to-amputate-healthy-limbs/ar-AA1MrQK7?ocid=msedgntp&cvid=68ce4014b1fe4953b0b4bd22ef471ab9&ei=78 they feel like they're an amputee in the body of a regular person "For...
Thread 'Did they discover another descendant of homo erectus?'
The study provides critical new insights into the African Humid Period, a time between 14,500 and 5,000 years ago when the Sahara desert was a green savanna, rich in water bodies that facilitated human habitation and the spread of pastoralism. Later aridification turned this region into the world's largest desert. Due to the extreme aridity of the region today, DNA preservation is poor, making this pioneering ancient DNA study all the more significant. Genomic analyses reveal that the...
Whenever these opiods are mentioned they usually mention that e.g. fentanyl is "50 times stronger than heroin" and "100 times stronger than morphine". Now it's nitazene which the public is told is everything from "much stronger than heroin" and "200 times stronger than fentany"! Do these numbers make sense at all? How do they arrive at them? Kill thousands of mice? En passant: nitazene have already been found in both Oxycontin pills and in street "heroin" here, so Naloxone is more...

Similar threads

Back
Top