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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.
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.
thank you! can i ask why do we need to do this on a denaturing gel? i dont understand because for normal running of dna bands, for eg after restriction digest, we dont need to use denaturing gels, so why does this method require denaturing gels?
use a transcription blocker and check whether you still get the high mRNA level or not. If you still get it despite of blocking transcription then the mRNA from the previous round of transcription (before applying the blocker) is not degraded yet.
I have a question please why does the part of the DNA that is blocked by the protein doesn't appear on the gel, ok i understand that part is protected but is it also protected from the flourescence ? I mean i think that the protected part should appear as an intact strand without any nicks but why is it invisible
You are very good at explaining in the most simplest way, thank you!
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You cleared the concept.. In few minutes, very effective, thank you
Keep watching the whole playlist.....all videos are carefully designed to have maximum impact in minimum time.
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Sure. Thanks
This helped so fast and effectively! Thanks!
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.
Thank you! Much better than my textbook
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Thanks for this explanation. Do you have any lecture on primer extension and S1 nuclease assay?
I Don't have one
very well explained, thank you!
Dont forget to checkout my entire molbio playlist. Link ruclips.net/p/PLKtiwIJ8Q7rppT2_xeMbIbrfTvAttgVcP
Thank you, very clear explanation
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Please make video on MLPA(multiple ligation-dependent probe amplification)
Ok i will try
amazing , thank you!
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.
Thanks... Subscribed.
why would those region not show any band, radiolabelled toh abhi bhi hai hi na vo dna ??
Thanks! Needed for a paper I'm reading for class!
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Very helpful!! Thank you
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thank you for helping me understand!!
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Thank you 🙏
Please share my channel link with your friends and help me to reach big audience
thanku so much very nice vedio with great picture quality 👍👍
thank you! can i ask why do we need to do this on a denaturing gel? i dont understand because for normal running of dna bands, for eg after restriction digest, we dont need to use denaturing gels, so why does this method require denaturing gels?
Thank you; this was very informative. Subscribed!
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Very very helpful thank you
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How to check whether high amount of mRNA is due to increased rate of transcription or decreased degradation in a cell?
use a transcription blocker and check whether you still get the high mRNA level or not. If you still get it despite of blocking transcription then the mRNA from the previous round of transcription (before applying the blocker) is not degraded yet.
@@animatedbiologywitharpan how can we calculate half life of mRNA?
Simple pulse chase experiments
Thanku verymuch
Please help me. I want a book that speaks " DNase footprinting assay 😢
Watson molecular biology of the gene is the best book in this context
Make video on Methyl interference assay please…….
Thanks for your suggestion, will try
G.O.A.T
I have a doubt for iit jam preparation can we use gerald karps cell biology for ur preparation
Vignesh Monika any text book is fine......you need the concepts ....does not matter which book it is
😁😁
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Sir please share Ur ppt
Ppt is not available for free
@@animatedbiologywitharpan how much is this ?
I have a question please why does the part of the DNA that is blocked by the protein doesn't appear on the gel, ok i understand that part is protected but is it also protected from the flourescence ? I mean i think that the protected part should appear as an intact strand without any nicks but why is it invisible
ya i also have the same question ❓