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❤
Great teaching ,I enjoyed it But please ,I couldn't get a particular word you were saying at 8:34,,,, did you say soluble??? Please I'll appreciate a response,, thanks in anticipation
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.
Good Day :) We are experts on protein purification and not the Golgi-Apperatus. We do not feel comfortable to answer this for you. What we do recommend to ask this question on platforms like Researchgate. You should find your answer there.
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 a master piece, believe me after a month in lab this is so accurate
Thank you very much! We appreciate that the effort that went into the video is recognized!
@@CubeBiotech well done , you deserve it .
I would be very happy if you do one for (Quantification of protein by Mass spectrometry) .
The video was really useful. One of the bests I’ve watched ever on RUclips 🥂💯
Thank you for the compliment! Great to hear that it was worth the effort :)
This is the most useful video I ve seen on this topic so far
Thank you very much. We are really glad to hear that!
good video, it breaks the concept down to a layman's understanding. you made education interesting.
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❤
Thank you very much for these kind words! That definetly made the day of the lead creator of this video! Thank you for further recommending us!
Such a good overview. Love the effort 🤩
Thank you! That was our intention.
Thanks really needed someone to explain this topic clearly.
This is really well made. Great job
Thank you very much :)
The video was of great help to me. Thank you
Thank you! Glad that we could help!
It was REALLY useful, thank you so much!
Thank you! Happy that our work for that video payed off :)
Well simplified. Thank you for the good work.
Hi Patrick, thank you for the positive feedback! That is always appreciated :)
03:38 precipitation method, salting out
Time stamps are set :)
This video is amazing and really helpful! Thanks :)
Really Glad to hear that. It makes us happy that the effort was worth it!
@@CubeBiotech 💜
Beautiful presentation :') thanks
Glad that you liked it!
Very Good and useful.thanks for describing so deeply
Glad that we could help :)
Many many thanks for this explanation ❤
We are happy it helped you. What part of the video did you find the most helpful?
Great teaching ,I enjoyed it
But please ,I couldn't get a particular word you were saying at 8:34,,,, did you say soluble???
Please I'll appreciate a response,, thanks in anticipation
Yes that is what was said.
"The protein is just soluble."
@@CubeBiotech thanks a bunch
@@elizabethmonday3751 You are welcome :)
This was really helpful 🙂
Thank you! Glad that you liked it.
amazing! good job! 🤩
We are glad that you like it :)
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.
Good Day :)
We are experts on protein purification and not the Golgi-Apperatus. We do not feel comfortable to answer this for you.
What we do recommend to ask this question on platforms like Researchgate. You should find your answer there.
Thank you so much for your guidance!!!
it is a brilliant video
Thank you :) We are glad that you liked it!
Thanks a lot ❤
You are welcome :)
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
Thank you for providing these additional information :)
SDS PAGE plz
Noted and thank you :)
❤️❤️❤️
We are glad that you like it!
❤❤😍😍😍
Glad that you like it :)
🥹🙏🏻❤️
can you send me the sides
There are no slides, sadly. These are, for the most part, Adobe After Effects files. :(