You just saved me from failing my lab report! thank you! I didn't grasp anything my prof was saying and this just made everything make sense
@ludovico_fusco2 жыл бұрын
EXACTLY the video I was searching for 😍 You used the same procedure my lab professor used, but explained it 100x better. I didn't even undarstand it was a BCA test until I saw this video...
@cwkgochan473311 ай бұрын
Thank you so much! I have no idea what was going on in BCA assay until I saw your video
@CR-uu1rr Жыл бұрын
Amazing video 🤩 😢Very detailed clear exhaustive you have taken away all my doubts . Spectacular step by step. Thanks a lot
@shinigemiX5 ай бұрын
Exactly what I was looking for, thank you so much 🙏 Amazing video 👍👍
@dhilipkumar9146Ай бұрын
THANK YOU HENRIK
@iontach98442 жыл бұрын
Thank you for an excellent and very detailed video. I have a question about when you mentioned extrapolating the data to work out the unknown protein concentration. Shouldn't you say interpolate instead of extrapolate as the concentration is being determined within the range of known protein concentrations from the standards based on their absorbance values and the absorbance value of the unknown protein sample? I really enjoy watching your videos.
@SpartanAegis2 жыл бұрын
An excellent video, concise with relevant detail too
@albertkuo5623 ай бұрын
this video literally save me ,thank u!
@chinenyeezeneche7838 Жыл бұрын
Thank you so much for the video. Your explanation was excellent. Please, does the linear curve indicate any meaning to the experiment? How do we calculate the protein concentration using the equation of the standard curve?
@henrikslab Жыл бұрын
Hey, thanks for that! The linear curve is of meaning to the experiment. You plot the absorbance value for each of your standard concentrations (use microsoft excel for that). If you have plotted the curve, you can see the formula of that plotted curve (you need that to calculate your sample concentration). Now, you replace "y" with the absorbance value of your sample and calculate "x". This is your sample concentration. Best, Henrik
@gabrieledomingosjardim535826 күн бұрын
But how do we calculate the concentration using the equation?
@sillygoose45322 жыл бұрын
Very good explanation!! By the way, did you do all the animation by yourself?!!
@henrikslab2 жыл бұрын
Yes, I did
@TheFlia2 жыл бұрын
Thanks for this informing video. I have a question. After getting the concentrations (I am getting them in ug/mL unit) should I have to divide to 20? Because I am taking 200uL from the working buffer and putting 10uL of the sample. In the end, should I divide to 20 or multiply it by 20?
@henrikslab2 жыл бұрын
If the device/program is not calculating the concentration itself, you would have to multiply by 20. But read into your device/program since many programs are calculating this already :)
@rrandaa1 Жыл бұрын
Maybe a weird question but what number at the end is needed to be multiplied by 20 and why? Trying to myself understand how to get results to mg of protein.
@sadpineapple41232 жыл бұрын
Gut gemacht mann!
@lovelyking9197Ай бұрын
I wanna ask that I have a sample in powder form, so how do I convert it into liquid?
@misakostic2524 Жыл бұрын
I am doing CSF prot.conc. and it is said to be 350µg/ml (micrograms per milliliter). This standard curve do not work so I am thinking to create 800/400/200/100/50µg/mL which is 10x more sensitive. Any thoughts if this will work at all?
@henrikslab Жыл бұрын
Can´t tell, I would suggest to try it out and look at the standard curve!
@unknownbeliever4660 Жыл бұрын
Awesome man
@antimatter312 жыл бұрын
What part of Germany are you from?
@henrikslab2 жыл бұрын
The area where I am from is called Ruhr area (german: Ruhrgebiet)
@openyourmind...2 жыл бұрын
Why 37 °C for 30 min ??? I believe that is not sufficient ...