How to calculate Protein Concentration of Unknown Sample from standard curve in excel

This video explains about How to calculate Protein Concentration of Unknown Sample from standard curve in excel
Simple method for the Determination of unknown protein concentration from standard curve in excel
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[@asiphenyabelemosha9345]

Me not expressing my gratitude would be wrong! I really appreciate this video. So simple, so quick and so straight forward. I've been trying to figure this out for the past three days and yet, you've helped me in less than 5min. Really appreciate it bro!!🙏 Keep it up👌

[@honourmukushi9427]

Thank you so much! This was so useful and I can't believe it took me so long to work out

[@sapnathebiotechnologist9167]

You are life saver ❤...I was very confused for this calculation but you saved me.. Thanks a lot sir🙏🥰

[@mohamedaimen4145]

Thank you saved a lot of time doing my homework !

[@tunanaa12]

Thank you soooo much!! It's straightforward and easy to understand 😊

[@aligacho]

ahh thats amazing and so quick, cant believe is wasted a week on sorting it out, thank you

[@flyingpotato9050]

THANK YOU👍🏼👍🏼

[@DJY217]

Thank you very much sir. God bless you 💝

[@kiran6097]

thank you so much. life saver!

[@tizianocadeddu3578]

Nice Job!!

[@sumreenapala4650]

Thank you so much sir ....very helpful

[@ilaydanuralras1715]

Thanks a lot, this literally saved my life

[@PRIYANKASONI-xg9gn]

Thanku so much sir..it helped a lot

[@bornoporichoi6751]

Thank u so much. I have to do this on next monday.

[@tanuchoudhary5644]

This is so helpful
Can't thank enough🙏

[@xapex5559]

you’re amazing. thank you

[@NegarsadatNademi]

its very useful for me thanks alot

[@RajeshKumar-qu7mo]

thank u for vedio please tell can we use your standard curve for analysis

[@heenasammi8919]

very informative
thanks sir for detailed explanation

[@BioResource]

Thank you. Consider Subscribing.

[@Poojajundiya]

thankyouuuuuuuuuuuuuuuuuuuuuuuuu sir 🤗

[@worldofinformation815]

Thank you, its great video

[@ko-fanta100K]

Thank you

[@dipakpakhre7122]

well explained

[@egs8545]

Thank you for making this!!!

[@Dearafia16]

Damn!! This is great... Thanks a lot

[@jamilah1534]

this really helped, thank you so much!

[@ballackey3116]

Amazing video thanks a lot!

[@kulsoomjaved1164]

Such helpful video 👍🏻

[@conceptum4250]

Thank you sir , Please make more videos on experimental data analysis like western blotting and PCR.

[@edenoosh9]

this was such a help. Thank you very much

[@mariorieraromo3703]

super usefull!!!

[@jadenhall1684]

super helpful, thank you!

[@premalathagattu907]

Nice explanation
And very useful video

[@BioResource]

Thank you.

[@ZeynepEran]

You're amazing man

[@babadhriti]

Very nice...

[@manendra3650]

thanks

[@Myopinions24]

Thank you, great video! But I don't understand how I should interpret the concentration after I calculated them? To what I should compare them? if I need to know the severity of the sample, what's the limit I should compare to? Is it the positive control? and how I say this sample is negative? is it negative with its concentration equals to the negative control or less? please help me :(( I have an ELISA report to submit

[@ishankagarwal4334]

The trendline should pass through origin as per the operating procedure. When chosing the option to display R^2 in the excel, there is an option to set intercept. Make it 0. The final equation will be of form y = mx. That is the calibration equation which needs to be used for determining the unknown concentration.
Hope it answer your question. Enjoy learning!

[@golamsarwar-26m17]

❤

[@Kinetic98]

how to calculate phenolic content by Spectroscopy ?

[@andreachen3052]

It’s a great video! Thank you so much! But when I calculated my protein concentration, it came out negative. Does anyone know what it means? 😢

[@endoprevvee]

me too

[@peteroyadonghan4442]

this might be because you have not diluted your protein standard to 1mg/ml if this is the case your absorbance value for your protein standard would be higher than 1 (into the range of 2-4). This is likely the case that results in a negative value.

[@ayeshakhan8219]

Sr how you calculated intercept value

[@hemadrivenugopal4836]

How to calculate the o.d reading at 660nm for 0.1ml,0.6ml.....

[@mrn6890]

Exam m computer ni milega intercept or slope value calculate krne k liye, manual calculate kr k b dikhana tha

[@DZreviews-ch]

@Bio-resource can you please tell me how to convert from ug/ml to ug/g of FWM, it's urgent please help me brother

[@richamishra9421]

If straight line equation is y=mx-c..this standard curve also considered as correct or not??..please answer sir

[@kawtheryousif5519]

👍👍👍👍😍😍

[@yangchendolmakom2230]

Can you give me the formula for determination of protein

[@katyayanicr2895]

In case of undiluted samples, shall we correct the OF with the blank or not necessary?

[@katyayanicr2895]

Sorry OD value

[@nguyenhoangtue8032]

what if the od of unknown samples is out of the od of standard reagents?

[@BioResource]

Hi,
You can dilute the unknown sample to fall into the standard's range.

[@sunitapaudel8673]

I got negative values while substracting....what does it mean?

[@ChayadaSongsakul]

Can you explain how do you find the number 0.34, .132

[@hugoavila9600]

Where is the negative 0 ug/mL control?

[@ishtiyaquekhan6068]

you need to adjust the content

[@BioResource]

Hi.. didn't get you. Could you please clarify?

[@maniaci907]

Its not a standard curve if you use a linear fit...

[@lindamckenzie5967]

Bunyi video tidak bagus

[@qussaialiraqi3661]

its not clear you have to details more..i dont like your explanation

[@bcollynz]

Thank you so much. This is so amazing

[@sewermama]

thank you