Detecting Proteins at 280 nm by UV-Vis: Why? How?

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  • čas přidán 28. 08. 2024
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Komentáře • 10

  • @RohitPant04
    @RohitPant04 Před 2 lety +1

    Nice job explaining the entire process along with the concept. Thanks!

  • @ioannaprasopoulou9016
    @ioannaprasopoulou9016 Před 5 lety +5

    Thank you very much for your video :)

  • @minenurayten2134
    @minenurayten2134 Před rokem

    great video and explanation!! thank you

  • @Lejonet120
    @Lejonet120 Před 7 lety +1

    Thanks for that, keep ON..

  • @kleineblumenvongarten5210

    Perfect!

  • @ZunairaFatimaWUM-BCH--
    @ZunairaFatimaWUM-BCH-- Před 3 lety +1

    Sir..plz tell me... the protein that is placed in spectrophotometer for measuring it's absorbance is with diluted ur diluted???....mean first of all protein from stock solution is taken and then diluted with solvent and then placed in spectrophotometer for measuring it's absorbance????..

  • @eunicetan5960
    @eunicetan5960 Před 4 lety +1

    hi what contributes to a more delocalised electron cloud such that it has a greater absorbance,why wont phenylalanine have greater absorbance since lone pair from oxygen can delocalise into the benzene ring ?

  • @amjadm6772
    @amjadm6772 Před rokem

    I'm confused about one thing. How can we come up with the calibration curve to begin with if we also don't have a proper way to measure the concentration of the samples??

  • @vasunakili5611
    @vasunakili5611 Před 4 lety +1

    Can we detected corona kind of protein