Agarose gel electrophoresis
Vložit
- čas přidán 1. 10. 2021
- In this video we have described the practicals approach of the agarose gel electrophoresis. The agarose gel electrophoresis can be used to check the quality and quantity of the macromolecules such as DNA , RNA and proteins. Here in agarose gel electrophoresis the separation depends on charge and molecular weight and in some cases also depends on the conformation of the macromolecules. The agarose gel electrophoresis is routinely used for the analysis of PCR products, molecular markers, genomic DNA, Total RNA and proteins. In short the agarose gel electrophoresis is heart of the biotech and life science students who is working on the DNA, RNA and proteins.
Here we have explained the most of things and minute details but due to time limit and the topic is vast so we have tried our best to cover the topic …!!!!!!!! THANK YOU !
Credits
Video shot by - VInayak Mohandas 👌
Assisted by - Anusha Raj
Edited by -ME 🙈
Well explained.. Kudos to the team..😊👏
Nicely explained🙌🏻🙌🏻thank you sir
Thank you for useful information 🙏
Very well explained 🙌
Thank you so much.❤ Tomorrow is my biotechnology board practical 🙏🏻
All the best 🙌
Thank u..This video helps me a lot...✨🙂
Well explained .. 💯❤️
Well explain bt background sound creats difficulties
Very informative video, keep it up, greetings from Germany!
very good brother , love from Pakistani ,Now Asia will rule ,West will follow .
Pls do share, it will encourage me to post more ! Thank you brother 😃
💀?
Chala baga explain chesav anna tq
Dear, its well explained....good to use "Gel Red" rather than 'Ethidium bromide'. gel red is very safe.
Thank you sir for your response in my previous lab i was using ETBR, currently we do use gel red only its very safe i agree and i do recommend !
Well done brother
Thank you sir.
Very much useful 👍👍 Pls upload more videos like this 🙌
Sure 😀
very good explanation
THank you ❤✌
You cleared all my doubts ⚡
Pls do share it will encourage me to post more ! Thank you 😃
Now i understand ..thank you
Pls do share it will encourage me to post more ! Thank you 😃
Thank you for your explanation 🙏🏻✨
My pleasure 🥰
👍🏻👍🏻
👍👍
Thank you
thank you sir so much... tomorrow i have board biotech practicals and you completely cleared all my doubts on how to do the experiment
All the best 😉
👍👍👍
👏👏
superb...
thank you 🙂
Keep watching
🔥🔥
👌✌️👏👏❣️
Well explained brother keep it up from Pakistan
Thank you dear 😊
🙌🙌
Thank you brother🙏kudos to you
Thank you 😊
Its a good explanation sir... Keep up it up❤🎉
Thanks a ton
Very nice explanation!
Thank you 😊 pls do share with ur friends family
Tq sir 🙏🏼🙏🏾
Thank you ❤🙏
Welcome!
well explained😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍😍. thank you
Thank you 🙏
Wow nice 😯😲
Thank you
Where is the gel image sir?
vyawahare.av@gmail.com pls dm so i can share
Very useful.... & i request u to kindly use a special microphone for yr clear voice.
Thankyou 🙏🏼
Thank you 😊 for suggestion i. Will implement it
It's very well explained practical..
thank you pls do share with your friends ☺️
@@lifereplicon ya definitely.. I already done
Thank you 😊 really appreciated 😃
Sir I need more videos which is imp in biotechnology field (techniques)
Sure 😃
Sir I want to learn about crossed over gel electrophoresis
Very useful please upload SDS page also
I will upload
Hi I'm having a doubt. How much 6x loading dye and DNA was added to the gel
Don't add to the gel 😐
Will it mix properly by centrifuger? And can we use vortex for this? Will it break those dna or not?
It will mix with brief centrifugation no need to vortex
✌✌
Very nice explanation. BTW who are from 12th sciences
Sorry I didn’t get you ?
Brother i am student of 12 th science and in biology we have DNA fingerprinting in which there is topic of gel electrophoresis
@dhairyatrivedi2306 i hope u understood !
Yes thanx very nicely explained
It was really nice.
Why two types of buffer used here ? If i use any one kind of buffer ( TBE/TAE) is any problem
Not at all you can any buffer which is available for you
Thank you
@@lifereplicon ok sir
Is TAE or TBE buffer is called running buffer?
both are running buffers
How much ethidium bromide did u add to the gel?
0.5ug/ml final conc
Every thing is very perfect but we can't hear your voice perfectly and moreover captions are not available so please make sure that your voice is clear to understand your important information sir
Thank you i was on low budget during that time
@@lifereplicon may God solved your budget problem now and wishing you to rock amazingly in CZcams
Pls do like s SHARE and subscribe ! I need support
Good but voice is not clear
I will improve thank you for suggestions
Bhai tum ye batao dye jb tum insert kr rhe to vo dikha na
Sab dhikaya hai na sir
etbr is added to buffer?
No its added to melted gel
@@liferepliconin well?
No in gel
It can be added , after whole process is done ...?
For just visualisation
No it should be mixed throughout the gel as the DNA or RNA. Can be visualise at anywhere in the gel
JUST IMPROVE VOICE QUALITY REST U R BEST
Thank you