Відео

دم شما گرم کلی چیز از شما یاد میگیریم

I hate my mine after seeing two girls licking coppter blades💀💀💀

ASP of QS5 in India is 15k and CFX 96 is 12k. Great video David. Let's compare NGS and Microarrays as well

can you explain how you figured out what volumes to dilute to get the known concentrations you wanted to make for the curve? timestamp is 4:54. you said its a 10 fold dilution? maybe this is a separate topic? do u have resources on how to do this part? sorry im struggling to figure it out as an undergrad, would appreciate it so much!!!

🤣👌

Sir what's is solvent traping and cold traping

Hello sir

But can you clone a RC car tho? Or myself?

Didn’t they say in show it was 99 percent pure so couldn’t the last 1% be what was making it blue

I'd say I don't want to live on this planet anymore but these chodes that call themselves the government wants us stuck in this level of mellow drama ... Anyway , the cloning process was done ages ago , the shit heads from India use it for human trafficking on a global level so that they can sell freshly cooked up kids to rich sadistic twats . P.S. fuck India for being the reason the world is a shittier place than before . The British should've gone all out on them to stop the spread of the cloning process of innocent people that were murdered .

Least informative

Very nice video! Are you familiar with Fluent script? Is it possible to add a video about how to use Fluent to do script for mixing different reagent in 96-384 well?

Dear Prof David, could you please put your email here , i want to ask you once i got the post run results how can i pick the peak and how to set the wavelength , know the unknown comcentration?

Cnform culorii urinei, ar trebui sa se consume mai multa apa.;)

The first cook they did was the typical clear ( Glass grade ) Meth .

will the whole plot is basically about guy who is capping so what is the issue?

What to clone? Short legs and square asses?

Hi there, can someone help me with the setting up calibration curve for TPH ranges ( C10-14, C15-C28 to C37-C40)? Of course the software is labssolution

Please make a video on performing a reagent lot to lot. The trainer for Access2 left before I was assigned to the run Access2 in my laboratory.

Good work

Lolll

😅😅😂😅😂😂😅😂😅😂😅😂😅😅😂can i clone on youtube? disappointed his face 😂😅😂

Hi David, Thanks for a wonderful explanation. Can I ask you how do you set up gradual elution in software? Many thanks!

fast and untuitive! maybe you can also show how to program a multiplex PCR with 3 different dye and the respective positive and negative controls? Thanks

is it really posible to clone human is there any trials conducted

Here also there are chances of collision how did you avoid that if you can let us know ?

Gracias

Thank you I’m starting fresh on the access 2

It is not expresso, it is espresso

So it will purg befor the injection ? Do i have to put it in the batch or it will run automaticlly

Hello sir, How to solve "The pump pressure Exide maximum" in HPLC

Hi! I'm learning how to use this software, but my main question is there's any way I can install it in other computer rather the main one connected to the machine?

Sir please make lab solution learning series including troubleshooting it would be very helpful .

Can u show us how to do an automatique intégration plz

Can u tell us how to do a régénération of column

when or what type of experiments is used explain .😁😁😁

What a legend

Thanks for that. Great job.

Sir manual integration bar not showing in program windows in postrun how to enable it

Is that i have to buy both plates for calibration? If my objective only uses sybr green

Thank you so much❤ From srilanka 🇱🇰

Maybe blue but its a bomb

Good video, your chemical biology?

Would you be willing to explain manual integration in the quant browser? I can't get my manual changes to stick for a mass data pull like this.

Much thanks

My first project when I started working at Thermofisher as a Systems Engineer was to do a benchmark experiment of the QS7 Pro, Opus, and Agilent. Qs7 Pro ended up having overall better performance and user interface. Also, there was a lot of bleed from Opus Filters for a few of the dyes I was using, causing bad reference CT value. Also, the Melt curve derivatives will varied from well to well i=on the CFX Opus leading a to a non proportional heating across the thermal array. The QS7 pro had more even thermal proportional across the array. I don't fully remember, but I had issues with the Opus genotyping analysis, im not sure if they even had any or a least the maestro software had limitations. I no longer work at Thermo and I have no stake in it. Just thought It would be nice to share. I moved on to the medtech industry and out of the biotech.

Thank you so much you just saved me!!!hahahaha 😂😅🫶🫶🫶

Hello David, Nice video. I couldn't find the video on the analysis of results from Quant5 and the software.

Hi David! Awesome stuff, you've been very helpful. I'm struggling to create custom labware (different well plates), do you know where to look/have advice for this?

Very useful