Mammalian cell culture

[@alexandracapodicasa1333]

Really great for someone who already has cell culture experience and just needed a quick crash course!

[@tareksyrian2423]

I can't agree more ! Exactly!

[@Ratseeker]

In other words, he is being waay to casual going about this to nitpick on. Haha But still a great video.

[@cutlerwhitely2269]

This is awesome, thanks! One note for anyone watching: Make sure you don't lay the pipette tip down with fluid still in it like at 11:05

[@mr.gmadscientist8859]

Thank you so much this was really helpful. Going to crush my interview now!

[@joel2757]

Great tutorial; it helped me to remember some basic stuff!!

[@carolinamendez254]

This is the best video I have ever seen. Many congratulations, for having put your best effort into making it happen.

[@JYOtiRaNJanMANgaRaj]

Thank u so much 🙏😊🙏🙏

[@albinaamangaliyeva756]

This is so helpful! Thank you so much!

[@MohammedAmeenah]

This is the best video have seen. Thank you so much

[@JoshIbbotson]

This is extremely useful, thanks Neil!

[@Zhi-u6j]

Very nicely explained sir thank you very much 👍

[@NewsIdeasInnovation]

Excellent video, very clear and informative.

[@alethea1158]

This video was very helpful, thank you so much!

[@Gts2pro]

Hi thanks great video , so we was taught to use aseptic technique by spraying anything going in the the fume hood ,

[@kosheeka]

It is always a good practice to keep following it.

[@amlmohamedelshabasy]

THANK YOU VERY MUCH I REALLY APPRECIATE THAT

[@home4429]

Super informative, thank you so much!

[@nikinajafi3823]

Really helpful thanks! I needed those tips

[@petersamuelemeka8710]

Very informative; step by step explanation. This is the perfect video I craved for. Nice work, Cross

[@SumiKhatun-y9i]

Great vedio for cell culture indeed😊

[@BlueSkyFight]

No trypandblue?😮

[@JosephKyalo-q5t]

Very good presentation

[@funny11744]

very informative and fast. very good technique! Could the counting be made without trypan ? It seems yes ,

[@kosheeka]

While it's possible to count cells without Trypan Blue, this method doesn't assess cell viability. Trypan Blue helps differentiate between live and dead cells, ensuring you're working with a healthy population.

[@vocalistguy9850]

Absolutely great

[@maggieweber8419]

Is it "safe" to pour cells out of the flask? Especially when working with primary cell lines, would it be better to pipette and avoid the flask's lip? or does it not matter?

[@kosheeka]

As you pointed out pouring cells out of the flask is generally not recommended. Pipetting is the preferred method for handling cells, especially primary cell lines which are more delicate. Pipetting allows for precision and reduced contamination risk.

[@stooteebaruah9678]

I had the same concern

[@aishahashmi2549]

Very informative 👍🏻👍🏻👍🏻

[@psirer..9625]

Thank you for the content.

[@sadiahaquekhan6003]

Hi Neil, I am facing contamination continuously in my cultured cell. I checked my media and My insect cell media which i prepared manually using 2x sfc media, gentamycin, P/S ,serum and cell culture graded water. Could you please tell me how can I know that which of any cell culture reagent having contamination or not?? I sprayed alcohol vigorously on the reagent bottles, holders, pipettor, washed my hand, wearing gloves, rubbing my gloves with alcohol, keeping my empty plates and plastic container under the uv inside the hood, still contaminated media... :(

[@canceronthebookss4975]

You can autoclave the media if you think any component of the media is causing it

[@kimmie2022]

Very thorough love this

[@taylormarkel1094]

this is so useful thank you so much for making this!!!!!!!

[@ZainAbbas-i3e]

wonderful and well presented. hope i could an opportunity to work under your supervision and guidance. i am final year student of biotechnology.

[@clairevernyuy5827]

Thank you very much. This is very explicit.

[@amansamriyar2480]

véry good explanation sir

[@b-harmony]

Thank you this was very helpful!

[@greencard1245]

I love your videos! thank you!

[@deepalishenoy6705]

Very nicely explained sir. Thanks a lot..

[@WhatsInAName0]

Very helpful 👍

[@marwatawfik3956]

thanks so much

[@shahnawaza6710]

Thank you for this nice video

[@danieloulhint7914]

Mr. Cross, thank you so much for this awsome video. It is really a review and informative for m.. Great presentation and easy to undersand. Kudos from Morocco.

[@funny11744]

What happens with the phenol red ( from the composition of media): Is the phenol red able to change its color from basic to acidic and then after pH changes from basic to acidic ?

[@kosheeka]

​@@funny11744 Phenol red actually can change its color from basic to acidic and then back again! But under two conditions it will not be a suitable component: 1. Multiple cycles of going from acidic to basic can degrade the phenol red over time, making it less effective as an indicator. 2. If the media becomes very acidic (much lower pH), the phenol red might not change back completely even if the pH is adjusted upwards. This is because the cells themselves might be stressed or dying, causing a permanent shift in the media's pH.

[@funny11744]

@@kosheeka thank you for information.

[@oussboudjelthia4869]

Thank you soo much!!!! That was brilliant

[@gitanjalideokar848]

Excellent efforts, very nicely explained

[@estefanycamilabomfimdossan2308]

This is an amazing work! Thank you so much!!

[@funny11744]

Question : Regarding the stem cell culture in T 75 flask - using media without CO2 : Can we use a closed cap for T75 flask ?

[@hebaomar3001]

Great job 👏

[@demonwolf6195]

Wait why would you wash the cell to remove the medium with the PBS? I mean medium is required for cell growth, why remove it?

[@kosheeka]

Washing with PBS removes unwanted components from cell cultures (dead cells, debris) and prepares them for further steps (staining, assays) without harming the cells. It provides a clean, consistent environment with the right salt balance for healthy cells.

[@saminathapa829]

Very good video , thanks

[@welelameka]

Thank you!

[@healthybutfathf8943]

When you filling the 96well plate are you doing reverse pappeting?

[@brunadepaula5640]

It was very helpful!! Thanks!

[@valev2839]

Thank you for this video, however I can't find the tutorial for counting cells :(

[@AdeelHassan-v1v]

extremely helpful

[@MES-S]

An informative video

[@prashantkumarparmanu]

REALLY GREAT .

[@arghavanjafarijozani2592]

Thank you

[@AmMalak-hd9di]

Why he put 1.2 instead of 120 ? Someone explain please

[@sarahmajin5358]

Thanks for this video👍

[@Cornbreadddd]

I serial dilution for that plating solution?

[@emilytravis2417]

How are the cells adhering to the flask enough so they're not dumped out with the fetal calf serum?

[@valev2839]

Because he is using anchorage-dependent cells, cells that only grow if they adhere to a surface. The cells are simply doing what they would do in vivo, inside the body. Cells that belong to tissues produce molecules that mediate both adhesion to the surface and cohesion with each other in order to actually form the tissue. On the other hand, red blood cells for example are usually in circulation in our blood so they wouldn't naturally adhere to a surface.

[@刘涛-c6y]

Does this really follow aseptic practice? I doubt that。

[@biologylover1565]

Nice sir it help us lot in COVID situation.

[@AmruMagdy]

[@hassangheisari5925]

Great video!

[@ISTARI22]

Can I ask if there are any cells in the dmem media that you throw out or all cells only adhere to the flask?

[@valev2839]

cells adhered to the flask

[@kosheeka]

Until we add trypsin in the culture the cells stick to the flask, but after the trypsinization step, your cells will be in the medium so be careful.

[@matthewwagner47]

Is breathing on it adding potential contaminating?

[@kosheeka]

Yes, breathing over the cell culture can be a source of contamination. You can introduce bacteria or fungi from your mouth and nose. In a sterile lab, wearing a head cover and surgical mask is essential to minimize this risk. Additionally, working in a biosafety cabinet provides further protection by filtering the air and creating a sterile work zone.

[@samratpaul25]

Are any animals killed during the extraction of Trypsin from their pancreas ? Or can it be done without killing the animal ?

[@louisjacobmoon]

Why?

[@samratpaul25]

@@louisjacobmoon the basic idea of lab meat is to avoid killing animals, so if you are killing an animal to get Trypsin or something out of them so that the cells can feed-on and multiply then it defeats the purpose.

[@neilcross9417]

Many now use recombinant Trypsin eg TrypLE www.thermofisher.com/uk/en/home/life-science/cell-culture/mammalian-cell-culture/reagents/trypsin/tryple-express.html?s_kwcid=AL.3652.3..e..o..tryple&ef_id=869904f24fa9112537fe6585ae811767:G:s&s_kwcid=AL!3652!10!76691033548341!76691086026937&cid=bid_clb_cce_r01_co_cp0000_pjt0000_bid00000_0se_bng_bt_pur_con&msclkid=869904f24fa9112537fe6585ae811767 However the foetal calf serum is most certainly animal-derived... There are some new but very expensive non-animal serum replacements

[@vijayaravindsubramanian9354]

Sir explain how insulin cells are produced and insulin injection are prepared

[@minato2363]

I guess the falcon tubes can be reused if autoclaved no need to incinerate them, I am saying this with respect to universities protocol no idea why its done in professional labs....

[@kosheeka]

The best practice is to avoid any type of cross-contamination during the study. Cross-contamination can be expanded to include chemical contamination that may occur if autoclave is not properly carried out. This is a common practice in many laboratories.

[@lisaoney1973]

Finally found a cure for my son Sickle cell I’m so glad you came into my life. I pray for long life so you can save more souls,Thanks #druromi .

[@mrx4814]

wow can you share your work or publications?

[@lisaoney1973]

@@mrx4814 Yes sure