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@faithdamercer5863 Ай бұрын

2100 Brakus Mission

@mennamotaz1101 Ай бұрын

You are amazing teacher. Thanks

@yabezD Ай бұрын

how to save a graph template like in ms excel, sir ?

@dennisparkinson6798 Ай бұрын

5190 Cartwright Common

@Mme_MiDoRi Ай бұрын

Best tutorial. Thank you very much ❤

@BarrettShirley 2 ай бұрын

805 Mills Lake

@shery4510 2 ай бұрын

Doctor how to prep tissue samples prior to analysis procedure ? For example If I’m talking about an actual bone tissue specimen, what are my initial steps.

@faranakmavandadnejad8307 3 ай бұрын

That was amazing!

@omoooooo4275 4 ай бұрын

Please provide more tutorials. I need your help

@my_workemails 4 ай бұрын

Thank you. Great tutorial.

@pksaini8107 6 ай бұрын

.TNF-alpha= 450 value - 0.132 Concentration - 11.792 Inme se result konsa hai.. please tell me

@goncalosousa8942 6 ай бұрын

I need to prepare a presentation about ELISA and your videos are saving my ass. Ty

@Breadsuperhero 6 ай бұрын

Hi is this applicable to direct ELISA too?

@lickmyballoonknot 6 ай бұрын

Thank you!

@GordonChao0508 7 ай бұрын

Does Competitive ELISA first coat antigen to well plate or antibody?

@mbalenhledlamini2632 7 ай бұрын

10 years later and this is still the best explanation I have found. Thank You!

@yahiasaddek8236 8 ай бұрын

Million thanks! I found this video very helpful

@futureddshanley 10 ай бұрын

Great Video!!!!

@julitequenum1128 11 ай бұрын

This is great. Simple explanation. Thank you so much!

@camozzip Жыл бұрын

prism 10 hack macbook

@numanahmed9300 Жыл бұрын

Great thanks. From Pakistan

@sanjaykumar-ew6mb Жыл бұрын

❤❤

@masio2605 Жыл бұрын

As an educator and a researcher, I just want to take a moment to appreciate how amazing you are with your explanations. Clear, concise, comprehensive. Simply amazing! Thank you so much for sharing your expertise 🤗

@Полина-и3з6в Жыл бұрын

Thank you very much! You just can`t imagine how this video helped me!

@lenardgonda9532 Жыл бұрын

I get that I am very late to the party with my comment. But can I just point out that our hero here woke up before 8 on a sunday, just to make a video of graphpad. Now thats what I call enthusiasm!

@zuha_tae_stan Жыл бұрын

very well described 👍👍👍👍

@agnesemans8654 Жыл бұрын

This video was very very helpful ! Thank you !!

@Exculibar7 Жыл бұрын

Thanks, help a lot!

@bingereader12 Жыл бұрын

Sir, you are a lifesaver

@luisenriquep.c.8752 Жыл бұрын

Man, you are the man. thanks for your help. Hi From Mexico

@nadirhussain948 Жыл бұрын

Helpful

@stickom Жыл бұрын

all fine until you plugged in 1/abs to x values.. can you explain that a little..

@MrSoloFlights Жыл бұрын

How long did it take ?

@siddharthm3283 Жыл бұрын

where is the 3rd part? is it still coming?

@ishtiaqahmed3785 Жыл бұрын

I have IDEXX ELISA kit for paratuberculosis. Formula is given there on brochure. OD values have to be incorporated in formula. But end results are confusing. I need help please.

@dxmerchant Жыл бұрын

Egad! What manner of Vacuuming Witchcraft be this?!

@SanaSaeed-hx4lg Жыл бұрын

where is the link to download Graph pad prism?i could not find it

@a.s9509 Жыл бұрын

Well. I couldn't find 90-well Plate Layout. There was no "print-outs" on your website.

@ruigfilho Жыл бұрын

Does It run on mac?

@ÁgataAdriánPérez Жыл бұрын

happy happy happy (voz de pito)...

@teodrop Жыл бұрын

Very useful! many thanks!

@weiliu3655 Жыл бұрын

Really helpful thank you very much

@sharpAXEE Жыл бұрын

What to do if curve fit equation has E

@BenjaminMatei-v8w Жыл бұрын

That was really helpful. Thank you so much! The problem I am experiencing is that Prism would just "make up" values for the readings that were negative or 0. Even though in one run I had a zero standard given with the absorbance and concentration of zero it would calculate a concentration of 50 for another sample that had the same absorbance?! Any suggestions on how I can prevent this, so that my interpolation will also just not give me any result for the samples at or below 0?