Bradford assay principle explanation
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- เผยแพร่เมื่อ 15 ก.ค. 2015
- Bradford assay principle explanation - This lecture explains about the bradford assay to determine the total protein concentration in a cell. This is a technique for the total protein test.
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he is the only youtube whos all videos are evergreen...
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I've tried so hard to understand Bradford assay, and I was looking for an easier way to understand it, and I finally found it. You're the best! I really like your videos.
You're welcome. Glad to hear that you're getting benefit from my lectures
More than perfect. I've tried to find a simple explanation for this assay, and this is it.
Thank you so much for this video! I have a lab report about Coomassie blue dye and this video really helped clarify how the protein-dye complex comes about in a way that is easy to understand.
thank you for simplifying the explanation. thank thank thank. very comprehensive.
You are an absolute legend, this channel is a goldmine of information. Cheers Suman.
Thank you so much for appreciating my efforts
Occam's razor mhmm
Really good explanation. Even English is not my fist language, I got to understand the principles. Helps a lot!! Thanks
Thanks for the explanation, it was very helpful. Great job!
very much useful for me. i hope sir, u will talk about that SDS problem in more depth in future... Thanks
great job explaining!!! i swear when my professor was explaining this i thought he was speaking german but now i def get it thanks again
thanks to you sir,for explaining this so clearly !
sir...plz also explain the lowrys method of protein estimation...
nd one more thing...u r the best..👍👍..ur language is very easy nd u r the last minute saver in our exams..
I need you as my biochem professor, ASAP. Thanks for these helpful videos!
great help before practical exams!! thanks a lot for the explanation Sir
Apnar video gulor range onek.... Biology related pray sob field ei apnat video ache..... Khub e help hoy eta dekhar por lab e gele
Thank you so much sir! I have watched your lectures alll the time whenever I met difficult concepts when i do assignments and read articles, and now I just joined this biosensor company and your lectures are still helping me!!!:)))
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Thankyou so much Shomu for helped me clearing molecular biology in the last sem🙏🙏🙏🙏
Thanks for the explanation!!
I like how he explain in detail your awesome suman
Yo! You're a life saviour! Thanks for the video. It is very informative!
+Julie Anne Dayrit thank you. Glad you liked my lectures
Well explained. Keep it up!
Thanks for the well organized lecture, what are advantages of bradford method for detecting proteins?
thank you now I Know the exact principle behind a Bradford assay thank you!
Thank you for the videos you make. May you explain the calculations concept of BCA assay also, by using excel.
Please 🙏🏻
I swear...his 8 yrs old videos works far better than present-day tutors
Obviously. No one can mat H the quality of Shomu's Biology
This video dug me out of a massive hole thank you !
Biology Guru man! Appreciate your lessons as a Bio student.
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EASY + HELPFUL, really thank you
Thank you very much.
Thank you so much for this great explanation ......😊😊😊 You are a fabulous teacher.....
Thank you so much for appreciating my efforts. Glad to hear that you're getting benefit from my lectures
Really good explanation ,thanks
D:
Shomu, you are the best
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Great video, helped me present at Lab meeting. Thanks!!!
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wonderful explain thank you sir
Thank you.
Please also explain how to generate a standard curve practically for both Bradford and Lowry assays, and my second question is how to know the concentration of samples once we have the absorbance of each (is it by using Lambert-Beer Law?).
My third question is about Standard Dilutions (What is it, do we make it and for what purpose?).
My last question is please explain these terms to me (Standard solution, control, treated, etc).
Yes...me too want the above information 👍
Thanks, it is awesome. :D
Thank you , Sir. It really helps me. Thank you so much
You're welcome. Glad to hear that you're getting benefit from my lectures
So nice!!
Thx a lot😭, you help so much for my persentation of Bradford!❤
You're welcome
Thank you Shomu, it was helpful!
You're welcome
Hi sir, thank you for your wonderful lecture, and I have one boubt... In this assay we measured absorbance at 595 nm, but in uv visible spectrum, blue or voilet will absorb at only 380- 430, then what is the mechanism behind this assay???
Thank you so much! It really helps my study!
You're welcome. Glad to hear that you're getting benefit from my lectures
Please make a video on protein estimation on Lowry folin method as soon as possible
thanks 🙏
Hi! Could you please explain why CBB in its unstable state is considered a cation when it actually has a lone pair of electrons, but is considered an anion once it donates its electron pair?
awesome !! thank you so much !!
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Will Triton X-100 hinder with the binding of dye and protein. Triton x-100 is non ionic detergent right?
Really good. thanks
You're welcome
thanks a lot
You're welcome
thanks shomu
You're welcome
super explained
Thank you
thank you .....very nice ...video
You're welcome
Thank you sir
You're welcome
Nice is Bradford reagent light sensitive..? Im doing in dark but still I m getting higher absorbance in blank? Can you plz help to resolve this problem?
Sir please explain standard curve of Bradford protein assay
Thank you.
You're welcome
can u tell me that change in color can also be generated if protein is degraded?
Well explained 👍🏻
Thank you
If the red unstable form is predominantly negatively charged in this state, then why is it 'cationic' seeing as I thought an ion with a net negative charge was an anion?
The CBB has many groups on its structure. In an acidic medium, all the three nitrogen atoms in the CBB are protonated and so they carry a positive charge, and the two sulfonic acid groups are negatively charged, so the whole molecule will carry a net positive charge. However, the molecule in this stage can still give a lone electron pair to the protein. When the molecule gives a lone electron pair to the protein both of them become unstable and they bind to each other by ionic forces coming from the electron pair being given to the protein making the CBB electronegative and the protein electropositive in the dipole moment. The interaction then is strengthen by the VDW forces. It is a very specific and complicated chemical reaction. I hope I answered your question.
response from Biomedical and Biological Sciences
Jose Cruz its very nice answer
Thanks for clarification
@@JoseCruz-en2ev let me clarify please, if CBB is already in cationic form ,then how could it be electronegative later? and amino group already have lone pair they must be protonated to get positively charge and here protein in taking lone pair of electron, ambiguous
Amazing
You're welcome
Sir but when Brilliant blue Has red colour it is in cationic form why there is negative charge then 🤔?
I video is very helpful
I have a simple question if the dye is in acidic condition how will it donate electron as in acidic condition it will act as an acid and acid are proton done not electron... Plz somebody can explain
explain lowery phenol method ......its very confusing so kindly make a vedio on tjis topic
thank u👌
You're welcome
better than professor like wow.
really helpful and easy to follow :)
Thank you.
I have a doubt, you told that in cationic form CBB is unstable and we know that in cation have +ve charge then why did you show CBB with -vely charge when it is unstable.
Why we are using only bsa protein .why we are not using another protein for this assay as standard protein?
why we set spectrometer at 595 nm
LEGEND
Thank you
I need anionic dyebinding method .......
plz shomu ..make video on microbiological assay ...1 diffusion assay 2 turbidometric assay 3 metabolic response assay enzymatic assay
+COC Lover thank you for topic suggestions. I will make that soon.
how can we remove sds from protein sample
we Can use Bradford assay to detect the NOx concentration
Sir can you please make video on Folins lowry method
Okay
@@shomusbiologyofficial Thank You
Please make video on lowry method also
Okay
@@shomusbiologyofficial tq sir😊
can you add eng sub?
Why specifically using BSA as standard
Clearer and simpler
You're welcome
Very well explained. But this video should have been named comassine brilliant blue and not Bradford
Okay. Thank you
Bhai Bradford assay ka Graf be bato
What did you study to know so much about this stuff. Did you learn it yourself?
+Gasper Kosmac I learned it myself studying
i had an assement ineed help
I beg your attention-
According to Lewis' Acid-Base theory-
a) An acid is an electron pair acceptor.
b)A base is an electron pair donor.
Now, you said that CB blue's unstable state is ACIDIC. but in its mechanism you said that , CB blue donates lone pair of electrons! Doesn't this contradicts Lews' Acid-Base theory?
😍😍✌👏🤘👌👍👐
*type 'Thank you!' 1000 000 times*
+mineral water great. Glad you liked my lectures
Speaks alot extra 😡 you just needed to explain the topic. Not about it's four ancestors
Thanks alot
You're welcome