Genetic Markers | RAPD, RFLP, AFLP
Вставка
- Опубліковано 10 вер 2024
- This lecture on genetic markers explains about RAPD, RFLP, AFLP markers and the use of these markers in genetic fingerprinting, SNP detection and plant breeding.
For more information, log on to-
www.shomusbiolo...
Get Shomu's Biology DVD set here-
www.shomusbiolo...
Remember Shomu’s Biology is created to spread the knowledge of biology by sharing through all this biology lecture videos and animations presented by Suman Bhattacharjee in UA-cam. All these tutorials are brought to you for free. Please subscribe to our channel so that we can grow together. You can check for any of the following services from Shomu’s Biology-
Buy Shomu’s Biology lecture DVD set- www.shomusbiology.com/dvd-store
Shomu’s Biology assignment services - www.shomusbiology.com/assignment -help
Join Online coaching for CSIR NET exam - www.shomusbiology.com/net-coaching
We are social. Find us on different sites here-
Our Website - www.shomusbiology.com
Facebook page- / shomusbiology
Twitter - / shomusbiology
SlideShare- www.slideshare.net/shomusbiology
Google plus- plus.google.co...
LinkedIn - / suman-bhattacharjee-2a...
UA-cam- / thefunsuman
THNX u alot sir ...u make my interest again in my sub...nd i m not reading from other notes jst watching ur videos now dayz nd i clearly understand every topic ...thnkuuuu so much Sirrrr .🤗🤗🤗🤗
It's nice to know
I come online and just check for shomu's biology. U make reading fun. Thanks.
is it biotechnology sub?
@@shomusbiologyofficial😮hdku😅❤n😊😢yo😮😊oy😅😮😮😊😢op ou
When always im in problm. .
its You Who take me away from that confusion. thnk u so much of u.
Thanks a lot for your lectures 🙏🏻 from Switzerland 🇨🇭
Thank you so much for appreciating my efforts. Glad to hear that you're getting benefit from my lectures
What would u do there ??
Your lectures is always capturing. Through you, I am beginning to understand molecular biology.
Im studying in an foreign country.
In every topic, that I had problem , I could find a tutorial Video of you about it. thank you very much to help us online and free.
I wish , that I could help your team in the future.
Your videos are amazing! So helpful. Thanks
You're welcome
whenever i search topics i put shomus biology at the end cause i prefer his explanations.
Thank you so much for appreciating my efforts
Watching your all videos in 2021 ❤️
You were amazing before years you r amazing today also 😎❤️😍
can you do a video about Sequence Tagged Sites (STS) and type of STS in detail!
SSR, SCARs, CAPs and ISSR and their differences!
thank you.
Sir thank you so much I finally got the concept of AFLP!
You're welcome. Glad to hear that you're getting benefit from my lectures
Thank you for the details, which some of the Ivy League lecturers also fail to add. Hello from 🇺🇸 ❤️
You're welcome. Glad to hear that you're getting benefit from my lectures. Please subscribe and share
Thank you so much! Your videos really help me revise everything a week before exams.
Thank you. Glad you liked my lectures
Thnx from algeria 🇩🇿🇩🇿🙏
Glad to hear that you're getting benefit from my lectures
Tq so much sir use me a lot keep doing vedios we will support you sir bcz u r a hard worker
Thank you so much for appreciating my efforts
I my responsibility to encourage you bcz i learn from ur vedio
Thnku soo much sir for your great explanation💐
You're welcome
Hey! Small thing I would like to point out. The rflp fragments you show on the sketch are all equal in length where you mark the RE sites. Wont separate on gel. :) Also the smaller three fragments would migrate much faster than the two large ones.
Thanks for the very well illustrated explanation.
Ur all videos are really help me a lot .....thank u so much sir ...ur way of explain and teaching is very good to understand each concept . really u r helping me indirectly in my csir net life science preparation.
Thank you for watching the lecture
Thank u sir💐 the way ur explaining is simply mind touching.
Thank you. Glad you liked my lectures
Can't thank you enough for this lesson! :)
Thank you so much for appreciating my efforts. Glad to hear that you're getting benefit from my lectures
Vry effective way of teaching... Hat's of to u..
You're welcome. Glad to hear that you're getting benefit from my lectures
Thanku so much Sir. These videos are real treasures
You're welcome
Thank you so much brother. You're doing a great job!
+Dhiman Hazarika thank you. Glad you liked my lectures
Thank you so much sir! REALLY HELPFUL 😊
Thank you, Sir.
From Bangladesh 🇧🇩
You're welcome
Very good for senior students and faculty who came from different specialization. Keep it up.
Thank you very much.
Very helpful...and also I have perceive some concep from your video thank you sir..
You're welcome
Thank you very much sir for making this video!
You're welcome
Congratulations for the great didatics
You're welcome. Glad to hear that you're getting benefit from my lectures
thank you so much for your videos! you're a life saver
sir thanks for helping us in zoology as optional in UPSC
You're welcome
tomorrow is my PBG exam.....thnq so much for making this video 😍........you are really a good teacher....whatever you taught us it seems like very easy and simple......bt in college I don't understand anything.....our college teachers even make a simple thing very complex
Thanks alot sir... Your video is very helpful for us
You're welcome. Glad to hear that you're getting benefit from my lectures
That was a great explanation...
very helpful!
thank you...
Your explanation is superb and understood it clearly ........super bro👌
Glad to hear that you are getting benefit from the videos
Thank you so much sir very easy explanation by u .
You're welcome. Glad to hear that you're getting benefit from my lectures
thank u soo much brother... your vedio saved my tym and was very helpul
thanks a lot sir, now I know the difference...
You're welcome
Tq sir for
watching ur Pdf lesson that provide me to understand easily... and give to multiple video lessons from different characters abt on biotechnology genetics relateds.
I miss your Frontech headphones
good at all
i skipped my genetic class 2 times and this video is very helpful, thank you sir!
That's a good news
Thank u . i just watch it and got much more idea about these stuffs .
Thank you so much ♥️
You're welcome
Thanku so much sir
You're welcome
thnk u soo much sir...it is vry helpful...nd it has cleared my all confusions....
Thank u so much sir this video is very helpful .
Thank you so much
You're welcome
Thank you very much. It is very usefull for me
Glad to hear that you are getting benefit from the videos
thankyou so much Bhaiya, helping me for tomorrow's genetic engg exam!
Thank you sir
You're welcome
Learning more than in school!
All the best
Thank you from Saudi Arabia 🇸🇦
Thank you so much for appreciating my efforts
Please also upload video on Use of ITS, MatK and rbcL in Angiosperm Taxonomy
Thank You sir!!💯
You're welcome
It Was so easy to understand. Thanq sir
The number of DYS what it does indicate ??
For exemple DYS394
Is it the molecular weight?
In the RAPD technique only the primer that is complementary will bind to the sequence ?
thank you very much this video has helped me a lot god bless you
+Nada Amr thank you. Glad you liked my lectures
You are great!!!!!
😀
Wow amazing sir u r so brilliant....
Sir for RFLP do we extract whole DNA of a cell (6+ billion bp) and restrict it with a restriction enzyme? Or do we extract only a part of the entire DNA and then restrict it? If so how do we do it
Sir RAPD ka kuch clear nai kiya kaisay kaisay marking main help karta hau
U r an excellent teacher👌
Thank you. Glad you liked my lectures
thanx for such nice videos... can us explain about how can we locate a mutation without doing an expensive genome sequencing
Hey.. The random primee tht we r destined to add in rapd fr pcr thereafter..is it necessary to do so.. I mn that the primer cn b run in pcr evn to gt aplified no directly..?????
Please sir make a video on "Maxam and Gilbert technique of DNA sequencing"
It's already made
@@shomusbiologyofficial thanks sir.. I'll search it
which type of nuclease enzyme is best to use for degrading all DNA in a sample??
plz explain
and one more
you want to degrade all DNA in a sample to avoid contamination..will you use exonuclease or endonuclease and what will be the reason for selection??
plz explain my questions
I have a doubt. In AFLP, if we already know about the restriction enzyme sequence flaking the sequence of interst, why do we need adaptors. We can simply use primers against those restriction sequences. Please do reply
Very good lecture but we have to should short discuss.
Explained in very simple language. Easy to understand.
But You've used only half of the screen. So board was not clearly visible...
Glad to hear that you're getting benefit from my lectures. Please subscribe and share
thank you for amazing explanation
It's like Raj Koothrappali got jealous on Fun with Flags.
LMAO this comment is gold xD
HAHAHA
Lol
😆
Brooo !!!!!! 🤣😂😅🤣😅😅
excellent explanation!
Thank you
I have a querry,...is it not that we don't require sequence information in AFLP too..just the adapter sequence is sufficient
May be, it should be known to select the particular Restriction Enzyme , which do not cleave our Target DNA. I don't know,it's just a guess.
Sir, please can you explain in Hindi video, please sir. 🙏🙏
I wanted this comparison... thank u....
Glad it helped
Thank you sir. It is helpful
Thanks
thank u sir....
happy new year sir
Amazing explaination sir.. thankyou
You're welcome
Thank u for the lectures.... But pls can u emphasize more on RAPD with more examples
after isolation of DNA from both control and stress plants. If we go for RAPD analysis of such DNA is any difference in the polymorsphism..?
Firstly thank you sir..how can be Target sequence identify
Thank you
Koothrappali kills it again!!
Excellent Sir.
wow unique explanation....
Thank you for teaching 😃 .
You're welcome
Well described.. but please improve your sound quality
trrwrrtowbcv b
thank u sir for simple explanation.. one doubt ..which genetic marker is called PCR based?
If multiple times target DNA present, since it has same length, rather than getting multiple bands, we will be getting dense bands ryt?! Pls clear that area sir 🙏
Thkuuu 👨 sir
You're welcome
Thanks man, awesome
5th day, 5th concept!
Thank you for appreciating my efforts
Thank you Bhaiya ji
Thank you sir, wish you have happy new year
Thank you.
U r the best 😎
Thank you for appreciating my efforts
Sir vntrs pay koe complete video nae hay apki? Sir must reply plz
Am unable to understand how random amplification of dna helps in preselection of breeds.Can u explain that concept further?
Hi sir you have tell about distinguish between these three techniques but this is not enough it requires more emphasis on how three techniques are different, this explanation seems like these three techniques are useful for same purpose, you should have explain actually what is the main purpose of these 3 techniques and how they exactly distinguish this is important thing because
In molecular biology techniques some times seems all techniques are useful for same purpose that's why I am emphasizing on purpose & distinguish
Thank you sooooo much stay blessed and keep making such videos... :)
+senorzorro12 thank you. Glad you liked my lectures