dont make a video on a topic that is not clear to you yourself

thank youuuuuu🙏 😭-a struggling brandeis student

Very nice presentation to tell me the determination of F and R primers!!!! Thank you very much!

Very nice

nice explaination

6:10 @stevenkitunshya

نريد الجلوس بجوار النبي صلى الله عليه وسلم في الجنة ....

thank you

Thank you for the detailed explanation

يعطيك العافية

Hello Herbert, First off, thanks for doing this tutorial, great help to me. I wanted to ask, why not just make it 18 base pairs because there's already a G assigned on the 18th position. Is there a reason for not doing the suggested?

C ONE, c-1

Can't see the whole video.

Volume for ants

I'm abit confused. How many nucleotides would be in his forward primer?

How to create the homology of that fragment

thank you!

What is meant by "chewing" the fragments, Ive never heard that term before, thank you.

Thank you sir ☺️this video was very helpful 😊

buy a pop filter bro

I'm digging for gold but found diamond instead, 8 years late, thanks for the videos!

Thanks a bunch for this simple and brief explanation. It was really interesting! Keep it up!

Look at the graphene structure, 6 points, 6 lines, and many of these sixes. That is the the mark of the beast 666. Also what can cause pain (Revelation 16:10) and a noisome and grievous sore (Revelation 16:2)? Only something medicinal can cause these. Not a chip implant. Also human body is 18% carbon. So therefore the number of a man is also 666. (Revelation 13:18）The sun shall be turned into darkness, And the moon into blood, Before that great and notable Day of the Lord come: And it shall come to pass, that whosoever shall call on the name of the Lord shall be saved. Acts‬ ‭2:20-21‬

Just what I was looking for!

1:00 "What I've drawn down here" Where? Can't see it.

Whatever happened to splicing animal DNA

kzbin.info/www/bejne/eJy3g4yDn96UqqM

Nice!

Tnx man

Why we need partial sequences while designing primer

Volume is impossible to hear anything. Did not continue to watch after 5 seconds.

Great video, simple explanation, thank you for this man!

sir thank you for this wonderful video! also if you could please speak louder next time because my volume was on max but you were still kinda soft

Every Scary Thing You're Being Told, Depends On the Unreliable PCR Test: kzbin.info/www/bejne/bJ_caqGEe62Eqbs

You helped a lot, thank you <3

could you perhaps make it a little quieter?

You. Are. Awesome. You just explained something that two profs and 2 TA's failed to be able to explain to me in such an understandable way. Thank you!!

thanks a lot

What is the advantage of not regenerating the enzyme sites

Where could I find explanation on what happens when primer binds to a different region of the plasmid with exact nucleotide sequence? How then that regions not get amplified to the comparable amount as the region of interest?

Would it be weird if you found an identical 18 nucleotide long primer in the DNA of a virus and a human? Anyone have a clue if this is common?

kindly reply me asap becoz it is very important for me to know that...

excuse me will u plz tell me that if i have a DNA sequence of 3819 bp and i want to make primers from this sequence then can i start from anywhere in the sequence or just for fwd primer i would have to start from begining and for reverse i would start from the end of the sequence??

What software is being used for the illustration?

sars cov2 primer

NOW AM INTERESTED IN THAT VIDEO BUT COULD NOT

It's nice explanation. FYI: I understand it's for better explanation, but the template you choose is quite short isn't it, so that primers actually overlap. I doubt these primers will work because they form dimers too easily.

very good video

Great Video. Short and really understanding

Thanks