Thanks - super helpful - haven't used a superloop in about ten years!
@johnsantos9754 ай бұрын
Thanks Brother
@tomgriffin43315 ай бұрын
Wow, Fitzkee Lab, that is terrific! Huge help. Thank you so much for the foundational idea and the cool variants. Great job!
@FitzkeeLab5 ай бұрын
Glad it was helpful!
@AerialOwens-uv5iq9 ай бұрын
Great video! Thanks for stepping through each of the processes in Parts 1 and 2. I generally use ccpn but the Sparky info is helpful too
@kannanp20009 ай бұрын
Thank you very much. I never thought of doing this through excel. This is very helpful.
@GMAdamFahmy249 ай бұрын
Thank you very much, man! I have a physics project due next week and I was really struggling with myself. You're a live saver :D
@ashishnandeshwar Жыл бұрын
This was really helpful 😮
@LeeGroupatCUDenver Жыл бұрын
Thanks, Nick. I can explain about some hiccups in the video. 1. UCSF/NMRFAM-SPARKY has some issues in the relative path resolution. Relative paths saved by them are incorrect if they are complicated sometimes. Latest POKY shouldn't have a problem. 2. Read peak list (rp) is an extension and not a built-in. It is in the Ext. -> Peak menu. It is the same both POKY and SPARKY. 3. Select visible labels (Lv) and peaks (pV) are in the latest POKY. Woonghee
@ericyoung7224 Жыл бұрын
Thanks for this!
@emdadsami2 жыл бұрын
Thank you Prof. Fitzkee for this lecture- Emdad
@Prince-oe6yv3 жыл бұрын
Thank you for this demonstration, exactly what I was looking for :)
@_ADHK293A_3 жыл бұрын
thank you for this contet
@odin-fr9et3 жыл бұрын
I remember learning this when i was in school. Something got me thinking about this today,thats why im hear. Thank for the video.
@mahmudulhasan143 жыл бұрын
Worth watching. Interesting chemistry. Thank you for this informative video.
@hariprakash44024 жыл бұрын
Please share more videos on Akta sample loading using Pump p950
@FitzkeeLab4 жыл бұрын
Hi Hari! That's actually something I don't have a lot of expertise on. My postdoc has used the sample pump in one of his former labs, but it was always one of the luxuries that we never purchased in the labs I was trained in. As a result, I built up some mighty strong forearms during my postdoc years!
@shadrums4 жыл бұрын
What's the process for putting protein sample into the loop next?
@FitzkeeLab4 жыл бұрын
The standard way is to load a disposable syringe with your sample (anywhere from 1-50 mL), attach a 0.45 um syringe filter to the end, dispense enough of your sample so that it fills the syringe filter and that there are no bubbles at the tip, and then simply inject your sample into the sample port in the injection valve. The default state for the injection valve, if no program is running in Unicorn, is the "load" state, which means sample injected into the load port will go into the loop as you inject. I never take this for granted, and I'm always looking at the super loop as I inject to make sure the stopper is moving up as I add my sample. I also look at the waste line from the injection valve: as I inject sample into the loop, buffer is displaced from the top of the loop, and that buffer gets directed to waste. Once my sample is injected, I can either start a program or manually run the sample. Most of my trainees do nickel and ion exchange columns manually these days, and we only use programs for our gel filtration columns, but either way, once the sample is in the loop, you can do what like from there. A final note: sometimes using the 0.45 um syringe filter makes it really hard to inject your sample: You're ultimately trying to shoot typically 25-50 mL of viscous solution through a tiny channel carved in the injection valve (not to mention the PEEK tubing). Even without the filter, injecting it carefully without breaking the luer lock fitting can require a lot of upper body strength and control. I always tell my students to take their time and take a break if their arms get tired. It's not a race. However, if the syringe filter is making things too difficult, a hard spin in the centrifuge at 20-40,000 x g for 30 minutes is often enough to get most of the large insoluble material out of your sample, and if you do this step you can usually eliminate the filter. Hope that helps!
@shadrums4 жыл бұрын
@@FitzkeeLab that was very helpful, thank you!!
@dxg13964 жыл бұрын
Thank you so much! I've been trying to do this for a while now.
@LeeGroupatCUDenver5 жыл бұрын
Nice. I will make an extension for a user to adjust user settings when I have some time to work on.
@LeeGroupatCUDenver5 жыл бұрын
... and it is here: kzbin.info/www/bejne/d5-aZHWqZZZgm5I 44:13 In the new GUI tool ("fP"), you can set to false for all strips. Then, leave the one that you want to have tick marks and set to true..