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

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  • เผยแพร่เมื่อ 16 พ.ย. 2024

ความคิดเห็น • 10

  • @RohitPant04
    @RohitPant04 2 ปีที่แล้ว +1

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

  • @minenurayten2134
    @minenurayten2134 ปีที่แล้ว

    great video and explanation!! thank you

  • @Lejonet120
    @Lejonet120 7 ปีที่แล้ว +1

    Thanks for that, keep ON..

  • @ioannaprasopoulou9016
    @ioannaprasopoulou9016 5 ปีที่แล้ว +5

    Thank you very much for your video :)

  • @kleineblumenvongarten5210
    @kleineblumenvongarten5210 6 ปีที่แล้ว +1

    Perfect!

  • @ZunairaFatimaWUM-BCH--
    @ZunairaFatimaWUM-BCH-- 3 ปีที่แล้ว +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????..

  • @amjadm6772
    @amjadm6772 ปีที่แล้ว

    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??

  • @eunicetan5960
    @eunicetan5960 4 ปีที่แล้ว +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 ?

  • @vasunakili5611
    @vasunakili5611 4 ปีที่แล้ว +1

    Can we detected corona kind of protein