for the sake of demonstration, just draw four different columns(ddATP, ddGTP, ddCTP&ddTTP) and cross check with the number of fragments obtained for all, remember from 1-8, there is no repetition and hence help in drawing the bands according to the length (sizes)of the fragments and that is how gel acrylamide electrophoresis works.i just got is also after serious observation .
Sir i have one question apne wo band draw kre vo kaise muje smjh nhi aya koi rule nhi he kya ya kis basis pe kra pls tell me i m confused in just that point otherwise i understand whole method....
Sir this concept is explained in a wrong way by Shomu's biology which is viewed by more than 24K. If you have approach to him, tell him to delete or remake video. Thank you sir.
Dear yousha thanks for this observation. But dear I can't tell someone that he is wrong. But I am glad that finally u got a correct explation. Please subscribe to our channel
Very nice explanation sir🎉
Nice and clear explanation
Thnku so much sir ji ur earlier vedio helped me a lot
Thanks sir for such awesome presentation. 🙏🏻🙏🏻
Great explanation sir 😊...Thank you
Awesome explanation sir👏👏👏
where the peimer goes? sir in test tubes you also start from the same sequence.ATG while you also attached the primer?/
Primers are dissolve
Thnku sir... It helps me a lot in my exams
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Great sir g
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awesome well explained sir 👌👌
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Clear explanation, thanks
How primer is attached?
Sir Please upload all topics of protein
You are awesome Sir..
Also need to the protein sequencing
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Thank you respected sir
Sir plz answer
How those bands are drawn?
Please watch video again and read book's
@@biovisionacademy3203 I also don't understand the graph
Good explanation. Upload more videos.....
Please do more videos for us sir.
Offcourse Saranya. Don't worry
Sir Ur vedio iz too much informative thnx alot
Thanks mam. Plz put yr suggestions and questions in comment section
@@biovisionacademy3203 sir why they stop the nuceotide ? Plzz...tell me how iz it possible
Free 3'-OH group is required for nucleotide addition. But due to lack of free OH. Group addition of nucleotide is Stop
have a nice day dear sir i think there is some corrections are required in synthesis of new DNA. in marking
Thanks
Gazb
excellent but mistake in the last steps plz told how you mentioned 5' and 3' in page electrophersis also
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Make video on meolecular markers and their application in animal and plant breeding
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Please make vedio on centimorgan
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Excellent video but mistake in last step some bands are wrongly draw😒
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@@biovisionacademy3203 plz check if bands are wrong
Thank you 🙏🙏🙏🙏👏👏🙌🙌
Sir how those bands are drawn🙄
By electro phoresis.
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Haan...I've done. But I'm unable to understand that section.😐😑
for the sake of demonstration, just draw four different columns(ddATP, ddGTP, ddCTP&ddTTP) and cross check with the number of fragments obtained for all, remember from 1-8, there is no repetition and hence help in drawing the bands according to the length (sizes)of the fragments and that is how gel acrylamide electrophoresis works.i just got is also after serious observation .
Sir i have one question apne wo band draw kre vo kaise muje smjh nhi aya koi rule nhi he kya ya kis basis pe kra pls tell me i m confused in just that point otherwise i understand whole method....
Same question
@@IrfanKhan-pk4pm am confused at this point too, who can help us out?
Sir en topics k notes
👌👌👌👌👌
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❤❤❤❤
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Baaki video bht achi hai par last step ki samajh nai i
Sir this concept is explained in a wrong way by Shomu's biology which is viewed by more than 24K. If you have approach to him, tell him to delete or remake video. Thank you sir.
Dear yousha thanks for this observation. But dear I can't tell someone that he is wrong. But I am glad that finally u got a correct explation. Please subscribe to our channel
@@biovisionacademy3203 I'll go for more videos and if your content is authentic and explained well, then I'll subscribe, not now.