Congratulations, I have never seen a tutorial as clear, detailed step by step and above all as complete as this one. Truly a lectio magistralis. Thank you, you are super.
you need to add something between the stacking and seperating so that your gel will be leveled. You can use isopropanol or butanol or simple DW, during the 30 - 60 mins wait time. Read Schagger protocol. Many issues.
Why did your gel lanes appear blue after running SDS PAGE? I mean when you dismounted the gel, the lanes looked blue and not much difference after staining?
Congratulations, I have never seen a tutorial as clear, detailed step by step and above all as complete as this one. Truly a lectio magistralis. Thank you, you are super.
Thank you, finally i understand total procedure.
Thnx this video change my life for better ❤🙌🏻
you need to add something between the stacking and seperating so that your gel will be leveled. You can use isopropanol or butanol or simple DW, during the 30 - 60 mins wait time. Read Schagger protocol. Many issues.
Very clear procedure. Thanks a lot
Thanks for u alot.. Egypt 🇪🇬
Excellent. Very clear. Thank you.
Why did your gel lanes appear blue after running SDS PAGE? I mean when you dismounted the gel, the lanes looked blue and not much difference after staining?
how to purify protein from adherent cells ?
The music 🔥
Excellent, thank you!
how much marker do you put on the gel?
0.75*
such a good video
Honourable Sir./Maam. I feel that it need to add yours video speech sub-title.
Thanks you so much...
This video is good but the music background is so disturbing
I agree it completely distressed me 😢