Extracting Plasmid DNA: How To Do a Miniprep
In this method video, Molly takes us into the lab to teach us how to purify plasmid DNA from a liquid culture of bacterial cells. When purifying plasmid DNA from a small volume (3 to 5 ml) of bacterial cells as we do in this video, this technique is called a miniprep.
View this video (and more like it) on LabXchange: www.labxchange.org/
Пікірлер: 65
This video is one of the best teaching for learning extraction plasmid.
I am not used to commenting but this one deserves a thumb's up. excellent explanation with clear and precise illustrations
This is a FANTASTIC video! Thank you very much, this was extremely well done.
@LabXchange
Жыл бұрын
Glad you enjoyed it!
This work deserves way more than that amount of view. Excellent work. Liked and subscribed!
The first time I understood what I was doing this whole time in the lab. Thanks for the amazing explanation!
The material in the video is amazing, and the scientist is also an amazing actress! Great job in here, keep up with your inspiring work.
Excellent Explanation, concise, and informative. Thanks.
Thanks a lot Mam for such well illustration! It helped me a lot as I'm a student of MS biochemistry
An amazing and fun way of explaining. Thank you very much. Please continue it so that many may benefit from your explanations
Excellent, detailed, and approachable presentation. You're a natural educator!!!
Gonna do this tomorrow this helps me a lot! Thanks.
this is a great video! thanks for the info!
perfect video. clear narration. overall 10/10
Hours of lecture and explanation distilled in to 15 minutes.
Thanku so much for this amazing video I really appreciate your efforts ❤❤
What an incredible science humans has developed. This is something to be grateful for everyday. Plasmid will have the potential to cure all diseases when the special interests will allow it.
Amazing explanation...❤ It covers each and everything you need to know. loves the way she explain.
That was PERFECT thank you for your explanation❤
protocol simplified and made interesting. kudos
Thank you very much! This was excellent!
Great video!😊
Excellent, thank you so much!!
wonderful demo
Super method of explaining lady (teacher)
Amazing! I love every bit of this video; so refreshing!
EXCELLENT WORK!!!
Every student like me deserve an advisor like you Mam 😅 Very well explained
Thank you for this amazing video!!! This channel will help me a lot
Amazing video!
This was super helpful, thank you so much
great explanation...
Best video in this subject 🎉🎉
the best video I ever saw
It was amazing, can’t thank you enough 🙏🏻🙏🏻
Thank you very much for the excellent video! It is very helpful!❤
It was excellent !! thank you ❤️
The best! Thanks a lot 😊
Amazing video.
Very well explained mam
Loved it thanks😊
Very informative. Highly recommended for molecular bio and genetics students. ❤ ill take my plasmids chilled served neat. 😂
Just amazing!
Thank you!
Thank You!
Thanks so much
How beautiful your video like your smile. I liked your video and your smile. Keep smiling and make videos.
thank you so much!!!!!
awesome! thank a lot
awesome
Don't get me wrong but I was here for science but stayed till the end for her smile
I loved it!
legend
what kit did you use, I have been trying plasmid extraction for months now, but I haven't gotten a reasonable result
Very amazing with a very pretty mam
Everybody got this? It's going to be on the test.
What happens if I forgot to wait for 1 minute before the last centrifuge?☹️
Which kit have you used?
You are so sweet and cool 🎉
Some of that equipment is filthy!
@bebolovesshrek
16 күн бұрын
How
Please do not inoculate your bacteria by poking a pipet tip by hand. Hold the sterile pipet tip with sterile tweezers (hold the tweezers in a blue flame for a sec) and then poke the colony on the agar. Also work under a flame or in a lateral flow cabinet.
@LabXchange
Жыл бұрын
Thanks for the feedback! In this video, Molly is working with media that includes selective antibiotic. If she were working without antibiotics, she would have used sterile tweezers. It's important to note that best practices can vary, so you should always check with your PI if you have questions.
I little bit confuse for Explanation O_o
Whats her @?