Absolutely marvellous video. Very concise, stepwise, explanation. Thank you.
@MarceloSMota-vi8zd5 ай бұрын
Very useful video! Thank you!
@sanjit6662 жыл бұрын
Nice crisp demo
@sara979792 жыл бұрын
Great explanation, thank you 🙏🏻
@HamdiAL-AZZANI2 жыл бұрын
Thank you so much dear brother
@parvizabdullah3 жыл бұрын
Thanks a lot for your explain. It was very useful for me.Hope you'll share new videos.
@innovative_learner3 жыл бұрын
You are welcome. Its a pleasure for me. Please let me know what kind of videos would you like me to post. Thanks.
@jesse48282 жыл бұрын
how do you get the raw data off the computer. all I can get is the report
@sufiyan50953 жыл бұрын
Thanks a lot for your explanation it's so useful Sir I have a doubt 3.29 what is that 50 below sample ID and beside DNA THANK YOU SIR
@정성훈-n9r3 жыл бұрын
What are the principles of nanodrop machines? I know you're using the uv-vis method. How do you measure the dna concentration and wavelength?
@SuleimanNasiru-ot3jy2 жыл бұрын
How can I use the values gotten to calculate the purity
@innovative_learner2 жыл бұрын
Please consult the following link for detailed explanation: dna.uga.edu/wp-content/uploads/sites/51/2019/02/Note-on-the-260_280-and-260_230-Ratios.pdf
@mohi75272 жыл бұрын
Hi, thanks for the explanation. Did you add Milli-Q water or DE water for cleaning the lens?
@innovative_learner2 жыл бұрын
Milli-Q water...thanks
@hanyabdelgawadabdelsalamab74702 жыл бұрын
Nice video, thanks for your help. Since you loaded 1.5 µl, is the result of the reading for 1.5 or for 1 µl ? ie the machine knows you loaded 1.5 and does the calculation automatically ?
@innovative_learner2 жыл бұрын
It's not about the volume actually. The liquid fills the gap between the two surfaces. Moreover the volume used was consistently same. No, you don't need to enter volume in the programme.
@bansisharma7203 жыл бұрын
What about concentration how to comment on the concentration we get at ug/ul
@jerrysworld82422 жыл бұрын
Same question. He didn't explain the concentration part