Site directed mutagenesis
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- เผยแพร่เมื่อ 16 ส.ค. 2015
- mutagenesis lecture - This lecture explains about the site directed mutagenesis including other techniques of mutagenesis like site specific recombination and transposition.
Site-directed mutagenesis is a molecular biology procedure that's used to make particular and intentional changes to the DNA sequence of a gene and any gene products.
Site-directed mutagenesis is likely one of the major techniques in laboratory for introducing mutation into a DNA sequence.
This video lecture deals with the mechanism and steps of site directed mutagenesis and the importance of side directed mutagenesis.
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its 2023 still no-one's got this much clear and good explanation on this topic
Glad it helped
Even in 2024, same
@@shomusbiologyofficialdo you mind doing a recent video on this?
Your animation videos work best.
Wherever my professor lacks, an Indian man will step up and teach me.
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I'm currently taking an upper-level microbiology research course and so much of the course material seems to fly over my head as though I have never heard about anything she is talking about. So far, your videos have made it much easier for me to follow along. Thanks, Shomu.
I'm doing a reu using a lot of biochemistry and this is one thing that we will be doing. I have never taken a biochemistry course before so your videos have been a life saver in helping me understand some of the papers I have been reading.
brother u are awesome u helped me so many times to study my exams one day before..thank u so much may bod bless u the good teacher
Wow Just Watched this One For Entrance Preparations.Must Say Even 4 years ago ur Way of Teaching is Quite Simple and Smooth 😄
Thank you so much for appreciating my efforts
Great lecture on the topic of site directed mutagenesis, thanks for the share, @Shomu's Biology.
Alternatively, it is used for investigating the structure and biological activity of DNA, RNA, and protein molecules, and for protein engineering. ---by Profacgen.
love from poland lots of salutations, i will pass my exam thanks to u and IgA and OG
All the best
You always been my last hope.
Thank you
Exactly ✨️
Thank you so much, I like the way you articulate your explanation with thorough explanation.
I don't know why all of my professors aren't like mr. Shomu. You make very complex sh*t very easy, Thank you sir
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Very well explained. Doubts clarified. Thank you!
Once again you saved me sir..... May Allah almighty sures his blessings upon you and your love ones... Love and respect from Pakistan...
👌👌👌😍
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You explain so clear, thank you so much !
Sir i am a biotec student of class 12 and only your channel helps me out in clearing my biotec based douts. Thanks sir
I am also biotech student
Explain very easy to easy understand. Thank you sir
Thank you for nice explain. I'm just start study about this topic and I'm so confuse. If you and your team have enough time can you explain about Iterative saturation mutagenesis?
Thank you
very helpful video. Very clear as usual. Thanks Shomu!
just now my sir my sir gave me this topic for my seminar I dont know single thing about this .and then I searched in your channel I found this .now I m very happy I know I will take my seminar well because your video is with me I will refer thaisthnkkuuuuuuuuuuuuuuuuuuuuuu sir
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Thank you very much.
I would like to ask if you do have a video about Triplet repeat primed PCR (TP-PCR), or if you can recommend a book or website that might help me understand it in details and thank you in advance.
Beautiful explanation as always
THANK YOUUUUU!! i have final exam in 6 hrs and i was lost you're a life saver💗
Glad to hear that you are getting benefit from my lectures
Nice work ! Now that I understand what was meant with "nicks", I can also imagine how the thing works with deletions and insertions. Thx a lot
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i like your teaching man its so splendid
Thank you. good presentation
Very clear, Thank You!
Just watched 1 hour before the paper and it helped me alott♥️👏
All the best
Nice explanation...I am mathematics student in Bsc. Now doing Ph.D in biochemistry so I have lots of problems in basic of biology...please suggest something how I clear my doubts?????😔😔😔
i see a drastic transition your course subjects ? any particular reason for biology preference ?
can I introduce 3-5 point mutations in this way? Also, do i have then design overlapping primers?
Would the nicks cause a transformation efficiency decrease? Would it be better to use T4 ligase prior to transformation?
Thank you SO much - this was so clearly explained!!
You're welcome
Sir, what is the difference between the Site Directed Mutagenesis and Single Nucleotide Polymorphism?
Please clarify
AOA dear Shomu! What will be the result if only a single primer is used with a change in a single nucleotide please. Thanks
muchas gracias aunque no hablo imgles me ayudo mucho....
Sir can u explain how the primer will bind to the double stranded DNA ?????
thank youuuu you are so good!
This is so helpful!! thank you for making this video
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Very well explained, thank you so much Sir
You're welcome
one confusion sir.. how will this primer bind with dsDNA..? do we have to first denature the dsDNA of vector.. as usual occur in DNA replication...?
bht acha explain keya h AP NY , but kindly types of mutagenesis bhi add kijye , thank u
Thank you so much I'll always watch your videos all are very useful to me thank you very much
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I'm really a big fan of you sir..!!
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thank you very much. m from algeria and this video helped me a lot
Glad to hear that you're getting benefit from my lectures
Hmm, I think for this overlapping PCR you forgot to talk about kunkel or Quickchange approach in more detail, downstream treatments such as DpnI or enzyme digestion are quintessential for the application and sometimes is better to add the disadvantages such as mispriming or primer dimer hybridization. A part from that you are always in every search on youtube.
great job!
shomu da you really help me to do my preparation for exams
Thank you. Glad you liked my lectures
I still wonder, if we would like to see the effect of mutation of a human gene, so does it mean we should insert the gene first on the vector and then we design a mutated primer for this gene?
is the klenow fragment that seals the nick instead of ligase?
Thank you man.
Your way of reaching is amazing....really💞
Thank you
It's actually a fantastic vedio 😊😊😊
Thank you
You are the best sir. Thank you
You're welcome
Ur explanation is simply awesome sir...😍😍
Thank you so much for appreciating my efforts. Glad to hear that you're getting benefit from my lectures
Shomu Sir, please come to USA and start teaching the students in this manner. I am very sure that you are better than the teacher here
Do you also provide material for GATE prep sir?
Thanks for such an amazing explanation sir ❤
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Thank you so much...
great....go on
thanks a lot
Happy Teachers days SHOMU . love you .ummahhhhhh
Thank you
TX DEAR 4 HELPING MY CEREBRUM
Thanks for the awesome explanation ✨
You're welcome
Thanku thanku thanku thanku thanku soooooo muchhhh sir 🙏🏻🙏🏻🙏🏻🙏🏻
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could you please make a video about signature-tagged mutagenesis? :)
watched this for my upcoming biotech exam on july 20th !
So how u wrote ur exam?
It was fine
@@shreyassehgal6849 i think u wrote ur exam in online?? Isn't it ?
Yes
R u from I mean where r u from?which group u taken??
Thank you sir for every thing
You're welcome
so helpful, make a difficult thing much easier
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Good job bro!
Excellent teaching thank you
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How to separate the mutated double stranded Dna from the parental dna that of plasmid???
First video in I love it your study R and d then I subscribe and for follow in like you like on your videos good man
Thank you so much for appreciating my efforts
Sir how two newly synthesized strand are combined🤔..
sir i have a doubt that in the video at around 4:28 you have said that its different primer sequencing and is not same as PCR but again at last of the video you had presented it as a PCR method..... is it a PCR based primer designing method or no?
Very nice .. thank you!
You're welcome
tysm ly Shomu
You're welcome
Thx sir
Can you help me with mutagenese with pcr! !
Congratulations for 2M subs sir!!!
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Thank you very much !
You're welcome
please do videos on PCR based site directed mutagenesis & cassette mutagenesis
Sr plzz upload a class on clb method of mutation detection
How do i set the thermocycler to achieve this mutation?
sir if we will change the particular sequence for mutagenesis their is a possibility of occurence of some genetic disease also ?
Thankyou so much sir
You're welcome
Sir, is it same with Tilling method?
Excellent ❤🎉
Thank you
Other parts are available or not sir
Sir, if you elaborate the full and another steps of Site Direcred mutagenesis. It will must help us to a broad idea about these topic. Thank you.
Okay
I didn't got your point....when usually replication occurs the daughter cell will have one parental and one new strand ....so how in this both newly formed joined??
mahrukh mahboob the newly formed sequences are mutated and are exactly complementary to each other the reason for which they form duplex
Sir I need linker DNA mutagenesis I am not clear about it please explain.
Tnqu sir 👨🏫👨🏫
Sir, please make a video on conventional mutagenesis
Loved it
Thank you
How will u take the mutated plasmid
Thank you sir👍
You're welcome
Thanksss for video
You're welcome
However , sir pls make a detailed video on pcr based site directed mutagenesis including.. overlap extension method,megaprimer PCR ,incerse PCR
Okay
Thank you ❤️
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well explained .. from Pakistan..
Thank you so much for appreciating my efforts
Thanks sir.... It's really very helpful for me
You're welcome
explain random site directed mutagenesis plz