This Video Explains DNA Sequencing - Sanger Method. Thank You For Watching. Please Like And Subscribe to Our Channel: / easypeasylearning Like Our Facebook Page: / learningeasypeasy Join Our Facebook Group: / 460057834950033
Пікірлер: 36
@Braindeadsoda Жыл бұрын
It is safe to say that this is the clearest video about Sanger Method I've found on KZbin by far, thanks for your work!
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@fairooz398611 ай бұрын
I couldn't agree more.
@raanamangrio3224 ай бұрын
Exactly same words by me
@pamom1002 ай бұрын
100%
@PomegranateDroid Жыл бұрын
Lady, you just rescued my Biochemistry grade. Much appreciation.
@EasyPeasyLearning Жыл бұрын
Thank you 😊
@ahmadabdullah29972 ай бұрын
God bless you I watched 3 lectures but could not understand the last part you made it clear Thank you❤
@EasyPeasyLearning2 ай бұрын
You are welcome 🤗
@thiagoamorim91617 ай бұрын
Omg, i love u, my apresentarion of Master's degree is tomorrow and I was confused on this topic. You save me
@EasyPeasyLearning7 ай бұрын
Thank you 😊
@bryanstapleton3119 ай бұрын
Im not sure if Im thinking about this right, but basically, since we can differentiate between fragment sizes based on the electrophoresis (assuming the gel can differentiate sizes of fragments by just 1 base pair), we can determine a sequence simply by analyzing where each fragment migrated in each tube based on the ddNTP? If that is correct, then how do we confirm the starting base pair of the sequence? I get that it would be the smallest fragment on the gel, therefore the band that traveled furthest, but that band can be a fragment that has 1 dNTP before the ddNTP, so that wouldn't tell us the very 1st base pair of the sequence necessarily. So in other words, how do we know that the smallest fragment had a ddNTP at the first base pair after the primer? Im not sure if that question makes since. But great video anyway, really clear.
@waterswater65442 жыл бұрын
Needed this last year): but thank u for finally understanding this😍😍😍
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@user-cp1kz4gp9k2 ай бұрын
To the point video ever found
@EasyPeasyLearning2 ай бұрын
Thank you 😊
@demianashenouda55906 ай бұрын
Thank you thank you. This was very easy to understand.
@EasyPeasyLearning5 ай бұрын
You are welcome 🤗
@raanamangrio3224 ай бұрын
Best explained
@EasyPeasyLearning4 ай бұрын
Thank you 😊
@mohammedal-hammadi50853 жыл бұрын
Thank you for the informative videos
@EasyPeasyLearning3 жыл бұрын
You are welcome dear
@jackwining19282 жыл бұрын
beautiful video, I'm currently doing my masters in Clinical immunology and was stuck on Sanger DNA method. THANK YOU
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@ruvimbomahewu39252 ай бұрын
Thank you
@EasyPeasyLearning2 ай бұрын
You are welcome 🤗
@fanfan976811 ай бұрын
How to calculate the number of fragments with different lengths? From short to long are N (Number of DNA template) x p (Termination probability), N x (1-p)*p ... ? Is it correct? why the band in the real gel is not like this?
@mehmethanarslan8829 Жыл бұрын
Thank you thank you thank uuuuu
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@dusk0135 Жыл бұрын
Thanks!!!! 🤍🤍🤍🤍🤍💗
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@spiritedzee11584 ай бұрын
My Goly, I get it!
@EasyPeasyLearning4 ай бұрын
That's great thank you 😊
@khalidaamir20463 жыл бұрын
Very nice
@EasyPeasyLearning3 жыл бұрын
Thank you
@coldsparks16622 ай бұрын
3:13 "when I added all those things in it" 😭😭 what things ?? please avoid saying vague THINGS like that . throughout the video, there were a couple vague words you used like that. Otherwise, the topic would have been clear .