Відео

Dload any course I need I ❤❤

Great !

Me gustpo

This video was very helpful.

they wrote to me that it cannot be obtained using a linear matrix product , what does it mean what should I do ?

Can you explain how to make TE 0.1X?

Why did you add gaga before primer sequence?

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

Very well explained..but last point i did not get, how 1ul enzyme for 20U.

which software you are using

ua-cam.com/video/iDkRhjdkFU8/v-deo.html

Great insight. Thank you for the free lecture

Shouldn't the concentration of the buffer be 2? Since we want 2ug of DNA?

Thank you for this video, what a nice thing to do. from Australia a big thank you.

The process was explained to us in layman's terms. 🙏🏽 ❤️

Thank you Sir, I tried to practice but can't find the cloning vector pTDL14.

Please first try to speak little louder.we can't listen ur words properly.

Thank you sir for th explanation

Very well explained it was so helpful made my day😇

amazing.

Thanks for the video! This really helped me to understand this program.

Thank you so much

This video ruined my life

Sir I have to add EGFP gene and our own diff promoters in this. So how will it be done ?

Thanx sir for making such videos

pogchamp

I was taught that you're supposed to pick two different restriction sites rather than the same one to make sure you keep the appropriate direction of incorporated gene. The way you presented means that some of the gene X fragments will be incorporated in the opposite direction, and without a possibility of selecting those out as they both would disrupt the tetracycline gene anyway, it seems useless to make such experiment...but nice effort!

please can you help me sir ?

The video i was searching thank you so much

Great explanation.. crystal clear..thank u so much

Thank you for such a wonderful presentation

Thank you so much! Highly appreciated! I can imagine, that you are very busy, but just know that you making those videos make a difference to some people and we would be happy if you would continue making this high quality contribution.

very good job

the process is not working

You are teaching electrophoresis, so keep maths out as it is 6 std stuff

thank you

Thank you very much !

Excellent 👍.

THE COYOTE THANKS YOU!!!

Thanks Man! BIG HELP

Can you please send me the excel sheets.

This helped me tremendously, so thorough

Can you help me Sir ?

Sir ... please make some new videos

Thank you, it was useful

Thank you so much sir, Really helpful video. cleared my basics.

Thank you for explaining very thoroughly

it would be nice to see how to install it on linux

You need to wake up first.

How the non identical part of the primers will be amplified?