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Came across this video and found it very interesting. I have a defect in the trpm7 gene and my health has been declining steadily over the past 15 years. Very scary. My Drs have no information and I’m afraid this may eventually be the cause of my death. Anyone out there know who I can contact to help?

🥹🙏🏻❤️

Thanks really needed someone to explain this topic clearly.

A cute animation that does a good job of describing what is happening :)

nice job but i hAve final exam after 5 hour clinecal bio chem 🤯🤯💀☠☠

I am working in a completely irrelevant field and this video was so good that is was possible for me to understand everything. Thank you!

:)

Thank you! - A biomed student in biochem

This is really well made. Great job

Very helpful!! Thanks so much!!😘

Great video! Are these magnetic beads reusable for multiple purifications or are they single use?

can someone explain me the affinity and specificity logic

Amazing 🎉

such a cute video and great explanation!! thank you <3

Super cute and helpfull, thank you! ❤

In native page , sds is not used , and proteins are. Not separated by charge only , but also by their Size and Shape ,. SDS an anionic detergent Provides The same negative charge per unit of Protein and Degenerates Its Complex Structure Into Linear One

This is fantastic

such a cool and interesting video! NEVER KNEW THIS!

This shit goes hard 👍👍👍

Well simplified. Thank you for the good work.

I didnt look up a vid to have to read...

This is the most useful video I ve seen on this topic so far

now say the chemical composition of titin

Hello r u life science student

thank you

Thank you for such an amazing demonstration. Please can you help and make demonstration on periplasmic protein purification in E. Coli. I think this demonstration is not available on YT.

03:38 precipitation method, salting out

C169719H270466N45688O52238S911

SDS PAGE plz

studying for my MCAT thank you!

Sticky ball😂😂

can you send me the sides

Many many thanks for this explanation ❤

So helpful!

Exactly 😂

Merhaba ben Türkiye'den bir aşı üretim kululuşunda çalışmaktayım.viral inaktif aşı üretmekteyiz.orotein konsantrasyon saflaştırma filtrasyonu (PEG) ve Kromotografi yöntemleriyle çalışmaktayız.sizinle irtibata geçmek istiyorum.

Vortexing protein?? 😱

Wowww I am beyond amazed. This lesson was explained to us in 2 hours and was so tiring and confusing but you managed to clear it all out in 13 minutes. So grateful 🙏🙏 definitely recommending this channel to my classmates❤

Thanks a lot ❤

Nice video. It clearly described FPLC in a very simple way and to the point. Thank you!

now pronounce the 12th isoform of it

Very Good and useful.thanks for describing so deeply

Great video! Love the animation so muchh!

Can I use one step purification FPLC?

I bet you’re from india

I do this In my lab with his-tag for bacterial pesticidal proteins. this explanation helps clear things up. if im not mistaken the reason we conduct dialysis buffer exchange after is to remove any excess imidazole from our target protein as it is toxic to the insects we test and may interfere.

This video is amazing and really helpful! Thanks :)

Hello from California! I have a question. Do Golgi in all types of cells (liver and kidney cells) have the same function and structure ? If we were to purify the Golgi ( fractionation) from different cells, (not plant) would they function the same and have the same structure ??? I can’t seem to grasp this concept.

I love it <3