I just want to say this thing.please continue making these videos you might have no idea that your channel is the best for clearing concept. So simplified way of presenting. Plz continue them
Great video, thank you so much! Maybe it is worth checking the enzymes and substrates showed in the box at 4:24 minute - there the Luciferase is listed twice. Is this intentional?
Thank you so much.Your videos are very helpful. I follow your channel regularly.I must appreciate your hard work.Very simple and clear explanation.Can you make videos on Next Generation Sequencing and biosensors?Please try.Thank you again.
Yes it is necessary to add apyrase at each step to assure that every extra nucleotide and as well as the ATP is degraded. According to my knowledge apyrase can only degrage unbound nucleotides and the bound nucleotide are not degraded by it and if apyrase is not degraded then I think it has no problem for boun nucleotides
I just want to say this thing.please continue making these videos you might have no idea that your channel is the best for clearing concept.
So simplified way of presenting.
Plz continue them
Extremely Helpful! Thank you!
Thanks heaps! This is the best comprehensible explanation I've come across
Amazingly explained! The concept is now crystal clear, would please make video on Next generation sequencing and microarrays?
This is such a high-quality chanal, amazing work! Your videos have helped me out often!
Thank you very much. You made the process really easy to understand.
Well explained, appreciate the effort. Thank you.
You are a life saver. Thanks.
Great breakdown; well done.
Well explained, appreciate the efforts. Thank you
Thank you for making this video. Brilliant!!!!
Your lectures are so good..really appreciable
It was helpful... thank you for explaining in such a easy way
Very helpfull, thank you !👌
Thanks a lot your all lectures are very informative 😇
This is awesome thank you so much
thank you for the amazing explanation, it is very clear
Outstanding!
Thanks a lot.You made it realy realy easy for me to understand.Before this I found i taugh.respect from Bangladesh🙋
An Excellent explanation. Thank you.
Super simplified. Thanks
Really Amazing and exceptional lecture
Best Video.. Thanks
Comprehensive thank you
Amazing lecture thank you
Amazing explanation thank you so much
Awesome, thank you
Thank you!❤
Very Helpful.Thank You
thank you so much, would be helpful if you uploaded a video on 454 pyrosequencing
Perfect, thank you sooooooo much
That helped me alot for my exam
Very helpful, thank you
Thank you mam for this lecture 😌
Greatttt! Thanks a lot 😁
Nyc explanation ever
excellent work👌👌👌👌
Thank you very much
Really helpful thank you
Fantastic. Best wishes.
great!!
It is really helpful :)
thanks a million
Thank you.
Excellent
Wonderful thank you mam ✨
Amazing
Very nice video
Very nicely explained
Life saver 😭🙏❤️🕯
Nice👍
TAHNK U SO MUCH
Can you make video on maxam gilbert dna sequencing
Great video, thank you so much! Maybe it is worth checking the enzymes and substrates showed in the box at 4:24 minute - there the Luciferase is listed twice. Is this intentional?
Bole to jhakkas
Thank you so much.Your videos are very helpful. I follow your channel regularly.I must appreciate your hard work.Very simple and clear explanation.Can you make videos on Next Generation Sequencing and biosensors?Please try.Thank you again.
Thank you for your valuable feedback.
The topics suggested by you will be added soon. Thanks
@@FrankLectures Thank you so much ...:)
That was helpful thanks! But how is this applied in instruments?
Hey!!!!! Why are not uploading new videos????
Amazing>> please , What is the name of program that using for making these videos. thanks
Is apyrase added at each step? If so then how is it removed or inactivated before the addition of next nucleotide??
Yes it is necessary to add apyrase at each step to assure that every extra nucleotide and as well as the ATP is degraded.
According to my knowledge apyrase can only degrage unbound nucleotides and the bound nucleotide are not degraded by it and if apyrase is not degraded then I think it has no problem for boun nucleotides
@@moqaddasbashir4034 but it can degrade the coming nucleotide that are not added still. How will u justify
@@MuhammadIslamag the rate of polymerization by polymerase enzyme is faster than the rate of degradation done by apyrase enzyme
mam please discuss the DNA library for pyrosequencing
gama3a shofoha wallahy fashekha
why dATP(alpha)s is added?? if anyone knows please reply with answer
Maam will it help in cracking jam exam
what about beads? Biotin? magnetic beads? PCR? Wells where it is loaded
No videos from last 2 years
10th new syllabus English medium types of fossilizalion explanation please send me videos
Mubeena
are you god or what
As usual, another good channel stops uploading...
Very helpful, thank you
Excellent
Very nicely explained
thank you so much I've been looking for such an explanation for a long time.