Helpful video, but NOT WEARING GLOVES WHEN HANDLING THE GEL MOST OF THE TIME! I'm not usually hung up on safety stuff, but in this case, liquid acrylamide is a neurotoxin, and exposure can lead to progressive peripheral neuropathy. You can never be sure that the gels are 100% polymerized. Kids - don’t do this stuff without a lab coat, safety goggles, and at least vinyl gloves.
I still don't understand why it's not allowed to have inner buffer leak to the outer buffer in this video. It's appropriate to overfill inner chamber and have inner buffer leak out in my lab and so is some protocols.
you are allowed that is to say, it'll work, im not sure if ALWAYS, but in the youtube videos put out by the bio rad manufacturers the electrophoresis demonstration involves overflow, I'm not sure if it was SDS though
You need to maintain constant flooding of the fluid on the gel, the fluid actually has different pH gradients from the outside buffer. If you have a leak you risk equilibriating the volumes and getting a dry gel, this can mess up the results. But even if it isnt a full seal it will still work as long as the gel remains flooded with buffer.
This video saved my thesis work back in 2014 and 2015. Thank you
A very explanatory step-wise tutor. Thanks so much
Thanks for assisting with my crisis after lab members went home :D
So nicely explained, I give this to my project students before they enter the lab :) !
Comprehensive and clear explanation. Thank you
Helpful video, but NOT WEARING GLOVES WHEN HANDLING THE GEL MOST OF THE TIME!
I'm not usually hung up on safety stuff, but in this case, liquid acrylamide is a neurotoxin, and exposure can lead to progressive peripheral neuropathy. You can never be sure that the gels are 100% polymerized.
Kids - don’t do this stuff without a lab coat, safety goggles, and at least vinyl gloves.
I felt like I was listening to my gearhead garage dad explain how to change the oil XD
Thank you for giving us the video version of detailed steps much better than reading texts that is so difficult to understand.
9:00 Don't panic,reload about 1mm between the space
Of well
Very professional explanation
Great video! Thanks for sharing!
i have a doubt . should the plates go in the space behind the ears or should they sit above the ears in the electrode assembly unit.
LOL @ 7:21
oh gosh, love it when that happens
Great video! Very insightful.
what is the advantage of choosing constant voltage over constant current?
What a constructive presentation
Thank you! This is extremely helpful
Thanks for this video........keep it up.......
Talk about precision.... ;-)
Thanks for upload this useful video
Wonderful Video
I still don't understand why it's not allowed to have inner buffer leak to the outer buffer in this video. It's appropriate to overfill inner chamber and have inner buffer leak out in my lab and so is some protocols.
you are allowed that is to say, it'll work, im not sure if ALWAYS, but in the youtube videos put out by the bio rad manufacturers the electrophoresis demonstration involves overflow, I'm not sure if it was SDS though
You need to maintain constant flooding of the fluid on the gel, the fluid actually has different pH gradients from the outside buffer. If you have a leak you risk equilibriating the volumes and getting a dry gel, this can mess up the results. But even if it isnt a full seal it will still work as long as the gel remains flooded with buffer.
There are 3 types of SDS PAGE, What's the difference between the 3 types?
1. Native SDS PAGE
2. Reducing SDS PAGE
3. Nonreducing SDS PAGE
IS NOT A TEST SIR
Thanks for this great video!
WHEN DID YOU ADD THE GEL?
He used a gel that its ready to go.
Thanks sir
awesome
Thank you for the video! It was really helpful :)
he didnt don gloves
awesome.. one of the best
08:13 That's a good load. Lol
Helpful indeed!
Nice instruction - but, why are you not wearing gloves!!
Тhank you!
its good
hhhhhm neurotoxins... wear your gloves kiddos
This is mine project
vietsub,please!