I live in the hazard.⚠️ ☢️ ☣️

I’m a living breathing biohazard.☣️

I spit my genes into genetically altered yeasts that I made to produce left handed sugars

You don’t want to know how I’ve been doing it.

Wow❤

The date is soooo important. You can refer back to your notebook to see what experiment you were doing!

Thank you very useful

Thank u

Perfect one for aspirants ♥️

AMAZING GRAPHICS TYSM

After the purification, I measured the concentration it was 1.82. and immediately ran it into agarose there was no band found. Please solve this problem?

Thank you! this was very informative and loved the animations.

Thank you, Addgene!

Okay but show us with cells tho

What types of purposes is there for cell culture other then figuring out the effects of diseases on living tissue

Is it possible to use tissue culture to make living human tissue? For example human skin? Or is a different method used to do so..

please explain in swahili

thank you

wow!

Simple, clear and precise video! Thank you for the explanation!

Thank you

428 Pansy Gardens

Ah yes takes me back to my first CRISPR kit and my garage setup...

Thank you for posting this. When attaching a single tip, one does not have to "screw in" the tip, but secure it with a very gentle twist. You might want to add that to the caption. I get a lot of questions about "how much pressure do you need to get the tip on securely"? I tell my students that, as long as their tips are not falling off, they are using enough pressure - your clear image of a properly seated, evenly seated tip is great. And, of course, the filled tip should be examined by eye, and the volume should look right. If one delivers the volume accurately and repeatedly, the tip is not too loose. Too tight, as you mention, is a different problem and should be avoided. For multichannel pipettes, the "rocky rack" method is preferred - gently rock the pipettor on the tips along the "long side" of the tips (i.e. each tip moves side-to-side with the same force) rather than along the short side (as shown in the video), where the edge tips receive more pressure than the central tips. The goal is to secure all the tips with the same force rather than have uneven seating and edge/loose-center effects. Multichannel filled tips should be visually examined.

903 Conn Islands

The video was very informative.

Как это учить?

A very clear and helpful explanation! Thank you very much!

Perez Charles Rodriguez Mary Anderson Eric

4:15 Wow, the gel is literally running from left to right! What kind of force pushes the whole gel slab to the positive electrode overcoming the friction? Why don't I see the running gel slabs in my experiments?

Kristofer Grove

So clear ans interesting. Thanks

TYSM , so helpful 🙏🙏🙏🙏

Well i found my first project

Excellent very didatic presentación!!

thank you for clarification.hats off madam

thank you for delivering clear information about the whole pcr proceduee

Cheer~~~not able to produce children or young.???😢

Veryclear explication thank you!!

Name him Mike.

1. 2ml screwcap 2. 50% glycerol 3. Liquid culture with bacterial growth 4. 1ml pipette tips 5. 70% isopropanol Add 500ul of 50% glycerol and 500ul of overnight culture to a 2ml screw yop gube Shake the tube 5-6 times

Thankyou for beautifully explanation

Thank you

Is it AICTE internship or not

🙏🙏🏻😊

She didn’t change her gloves when she handled the gel and then touched the microwave .. yikes contamination factor

What is the purpose of the aspiration tube?

Sorry but I can’t take someone who clearly has no clue about aseptic techniques seriously when they’re trying to show others how to be aseptic in the lab/cleanroom lmao

Should i use nutrient broth instead of LB for Bacterial DNA Isolation @Addgene

V good