Відео

Congratulations from CRB1 Patients Association Science Observatory Spain!

A great day indeed!

Positive reputation only with deleting the real experiences - but people talk 😂

Pitch black via capacitance Cometary Lighbolt drawn path least resistance no interference myriad stars charge distributed twinkled into depths morphed instantly Green Plasma Accretion Disc inside upright Naga form ideal warping transmuting Globular Filamentary Galactic Cluster retracting hardy under entropy working towards destiny against resistance devouring enemies conditions faced keeping biorhythmic evolutionary path!

i wish there was an english ttranslation

Can I use Epredia cryomatrix or Richard-Allan Neg-50 as a substitution of OCT?

$TXG -90%

stock in the garbage

how do you get the nuclei suspension? i failed at this part all the time.

❤❤hidden half of life!!

Love the music

Anyone else here because of _Half-Life?_

When you say, “damn these people are smart” out loud mid video. Really impressive.

Thank you for this video.

En español por favor

Como se usan por favor hay quien mede esa información

Wow

Good instructions

how much this ?

how do we know cell types through using scATAC-seq?

Great tutorial. I do have a quick question here, I have a gene of interest, how do you find what cell type express this gene of interest in loupe browser?

First

First

First

First

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Thanks for the explanation!

Amazing 🤩

Great thanks 👌

Thanks for the video, I suggest this video for more information ua-cam.com/video/Nsn_ZpDVBk8/v-deo.html

Brilliant!

Why is it re-uploaded?

very useful!

ᑭᖇOᗰOᔕᗰ 😏

Do you think isopentane would have reactivity with ceramic beakers?

thank you so much! excellent demonstration, you are awesome!

Why are the stocks are so low?

Need more people so spread this video more

How do you know the orientation of the OCT frozen block once you remove it from the cryomold and place it into the sample container? Can you label the frozen OCT block?

How do you pop the bubbles if you accidentally introduce bubbles? I tried using a needle but couldn't didn't pop all of them.

Thanks for this great video!

If my tissue is very small embryonic transparent that cannot transfer it by forceps its can be in eppendorf as pellet what should I do:- 1) put isopentane in container in liquid nitrogen and put eppendof that have the tissue in the isopentane 2) mix the embryos tissue with isopentane in the eppendorf and then emmerse it in the liquid nitrogen, in that case how to get red of the isopentane if it is necessary

menopause at 70? yes, targeting specific genetic material and than without freezing the eggs import (food) the new, improved genetic material and working on mindset.

This method worked well for fibrotic mouse muscle. Thanks!

is there a way to do this with liquid nitrogen instead of dry ice?

Just checked the most up to date tissue list...no plants included. That's too bad, I was hoping to find Arabidopsis there.