Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
Really glad to know it was useful. Please follow my instagram page and facebook page. Please share my youtube channel link with your friends and help me to reach big audiance
okay. Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
In reality pcr amplification of a fragment more than 1kb is difficult because of the relatively low fidelity of Taq Pol. So its better to say the chances of amplification of big fragments ( let's say 2.5 kb ) is low.
All of your videos are brilliant
Thanks a lot for working hard for all of us .. 🙏🙏
Thanks a lot for the complement.... please share my channel link with your friends and help me to reach big audience
So much needed video 🙏
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Thank you sooo much... Really needed this❤
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Already done..
Recently found this channel. Very lucidly explained and the animations are also very good. Please keep up your good work.
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Thanks sir for great guidance in short and easy form your video makes my genetic engineering study easy and good 👍 thank you so much
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Your MOL BIO related short videos are very helpful....
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Nice video ...short and crisp..👏👏👍😁
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I have videos on a wide variety of topics please checkout my playlists
Thank you sir it means a lot
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i finally understood!!! thank you so much
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Thank you sir. very helpful 😁
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Very good
Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
What are dominate markers and how they didn't differentiate between heterozygous and homozygous
How do you design the primer if it doesnt need to know the actual sequence of the target?
Useful.. Thanks
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Your videos have been very helpful, sir.. Can you provide the source for study material on the topics, please 🙏
all are from fundamental text books like molecular biology of the gene. Lodish, etc
Sir, do video on AFLP
okay. Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
The random primers that are used.. are they same if we do RAPD to compare two individuals DNA ?? Plz rply ...
omg did you ever find out lol
can you please explain why amplication dont occur when the primers are far apart ?
In reality pcr amplification of a fragment more than 1kb is difficult because of the relatively low fidelity of Taq Pol. So its better to say the chances of amplification of big fragments ( let's say 2.5 kb ) is low.
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i read that amplification wont occur even when the 3’ends of primers are not facing each other ? can you please explain why ?
for sure . thankyou soooo much
Do you have a pdf about that?
The Pdfs are not available for free