thanks for the video. A clarification (either pinned chat or extended video) on homolog scale would be great; meaning - what you showed us was taking chromosome as a whole but what about the portions contributed by the father and mother ?! In that case, we will have two blue and two purple strands.
Dear sir, please put a vedio on random priming, end labelling of DNA and RNA , non isotopic labelling and detection. I have been following ur vedios regularly and uts quite hard to see some other vedios for learning. So it's a kind request to add these vedios as soon possible sir.
How do we get to know that which Restrictions enzyme I need to use? Like do I need to already know the polymorphism in the dna of 2 individual and then from that I will take a RE which will cut only in one individual and not on other?
no, its based on chance. We will simply use different restriction enzymes and see which one cleaves one of the fragments. Then we compare it to the other fragment to see if any cut is observed. This is detected by agarose gel electrophoresis
Maine har roz 2 videos upload kar raha hoon. Hit the notification icon after subscribing. Just uploading damage and repair videos. Stay tuned to know more
Thank you for video Does it mean that we should be knowing the sequence of that DNA on which specific restriction enzyme will work ? So from whole genome we have to take that 0.1% different and known sequence ?
We use specific restriction endonuclease that can cut different number of fragments as they cut in their marked location in target dnas. This process works as there is specificity of the enzyme
But suppose both the individual do not contain GAG then there will be same band in both how will we identify then, because if they do not contain this seq that doe not mean they r same so then use of this enzyme will be of no use ...
How come genetic markers can be either dominant or co-dominant? Do not we imply the term "dominant" or "recessive" to the products of alleles (i.e. product of genes; proteins) ? It would be dominant where the gene would be expressed and recessive where gene would be not expressed, irrespective of the presence of the specific genetic sequence? how come then RFLP is a dominant marker?
Sir agar Covaccine ki duble dose lene mein kisi karan se 2,3 month late hojata hai to kya fir se first dose lena padega ya duble dose le skte he Plzz reply
I've opened this video for comparing yourself with your old videos actually , I was learning blood pressure ...
Well explained !!!
Thank you
Best teacher in the world 🙏🙏
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All tym favourite teacher 🤗 God bless uhh sir 🤗🤗
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Very well explained. You keep it simple and have good clarity.
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Watching your all videos in 2021 ❤️
You were amazing before years you r amazing today also 😎❤️😍
Im so glad you started uploading videos again
I never stopped uploading. In fact I have uploaded more than 100 videos this year
Your vedioes are always helpful for me !!
Thanks 🇵🇰
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Thank you so much sir...this was a best lecture indeed ❤😊
You're welcome. Glad to hear that you're getting benefit from my lectures
Zabardst...kmaaal lecture....greatest
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Thank you sir you are my favourite teacher
Glad you liked it
Sir. you are helping us a lot.. I will be very thankful to you for the Study. Thank you 💞💞💞👍👍🤗 Excellent lecture sir...
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Thanks sir..
Very useful classes...
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Good Explanation
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👏👏very helpful video sirji
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Thank u sir ...we r waiting for more markers v
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Thank you sir 🔥🔥
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sir it helped me a lot
You're welcome
thanks for the video. A clarification (either pinned chat or extended video) on homolog scale would be great; meaning - what you showed us was taking chromosome as a whole but what about the portions contributed by the father and mother ?! In that case, we will have two blue and two purple strands.
very essay way to learning thank you bhai
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Thankyou so much sir ❤️
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Thank you sir 😁
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I don't understand hindi but still watch them all🙃
Thank you
You are absolutely pagal
Same here😌😇
Coz ur interested in him 😏
Thank you sir
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Awesome 👌👌👌👌
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Great 👍
Thank you
Dear sir, please put a vedio on random priming, end labelling of DNA and RNA , non isotopic labelling and detection. I have been following ur vedios regularly and uts quite hard to see some other vedios for learning. So it's a kind request to add these vedios as soon possible sir.
Thanks alot sir
You're welcome
Very nice.
Thank you
Thanks
You're welcome
Sir please make a video on transposon tagging.. Much needed for exams.
Okay
How do we get to know that which Restrictions enzyme I need to use? Like do I need to already know the polymorphism in the dna of 2 individual and then from that I will take a RE which will cut only in one individual and not on other?
no, its based on chance. We will simply use different restriction enzymes and see which one cleaves one of the fragments. Then we compare it to the other fragment to see if any cut is observed. This is detected by agarose gel electrophoresis
thank u sir
You're welcome
Sr why we didn't use pcr and use agarose gel?
Best 💯
Thank you
Thank u sir...
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Sir after Gel electrophoresis we done Southern hybridization right?
How ladder is prepared? what if we pcr the ladder, does it multiply?
kindly make a video on dna mitochondrial use in forensic
Okay
Again watched and again kmaaalll
Thank you so much for appreciating my efforts
@@shomusbiologyofficial genomic DNA digested with restriction enzymes. Isme digested ki smjh nh i.
Deal?
How do we get to know the sequence of that 0.1% difference between those individuals
Where i can find the English version of this video ?
Aapne videos upload karna q band kar diya bhaiya plzz dna repair and damage pe video daal do
Maine har roz 2 videos upload kar raha hoon. Hit the notification icon after subscribing. Just uploading damage and repair videos. Stay tuned to know more
❤❤❤❤❤
You're welcome
Sir please start immunology,developmental biology full topic for bsc MSc students
Thank you for video
Does it mean that we should be knowing the sequence of that DNA on which specific restriction enzyme will work ?
So from whole genome we have to take that 0.1% different and known sequence ?
We use specific restriction endonuclease that can cut different number of fragments as they cut in their marked location in target dnas.
This process works as there is specificity of the enzyme
Okay now I got it
Thank you so much
But suppose both the individual do not contain GAG then there will be same band in both how will we identify then, because if they do not contain this seq that doe not mean they r same so then use of this enzyme will be of no use ...
Thinks sir please upload more lecture in hindi
I humbly requested to u
Thank you
How come genetic markers can be either dominant or co-dominant? Do not we imply the term "dominant" or "recessive" to the products of alleles (i.e. product of genes; proteins) ? It would be dominant where the gene would be expressed and recessive where gene would be not expressed, irrespective of the presence of the specific genetic sequence? how come then RFLP is a dominant marker?
Sir agar Covaccine ki duble dose lene mein kisi karan se 2,3 month late hojata hai to kya fir se first dose lena padega ya duble dose le skte he Plzz reply
No. As per govt rule one more dose will saffice
Good
Thank you
Sir plz make video on methods of cispr cas 9 gêne editing
Okay
Tq hindi me banane ke liye
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Love from Pakistan
Thank you
Can you provide an english video?
Already made
@@shomusbiologyofficial can you tag me the link?
🙏 After long time I watch your video. Due to some reasons I couldn't. When will be held this CSIR NET exam 2021.
Not announced yet
@@shomusbiologyofficial Ji Sir
👍👍👍
Thank you
Please make more Hindi videos...
Okay
Sir i dont understand Hindi please as previous videos explain in English..thank you
English version is already available
@@shomusbiologyofficial thank u sir
Sir kindly please upload videos in English only, regards from tamilnadu.
Sir I would suggest you better make video with English,,,thank you sir
English videos are there already
Why hindi?
Already made this in English
Not understand
Sir hindi me notes chachiye
Sorry. We can provide it in english only
Sir explain in English plz
Okay
Gag pe q kata
Nooooo why speak hindi 🥺💔
English version is already available
@@shomusbiologyofficial yeah i saw it 😍😍 thank you shomu
Thanks alot sir
You're welcome