Running an Agarose Gel - University of Leicester

[@tylerlott509]

This is a very high quality video.

[@zhehanli6689]

thanks for noticing

[@imanbrema7535]

Tyl666 666 de 666 6 6 666 6 66 de la 66 de la semaine prochaine pour le moment de la la la la semaine er Lott $$¥[

[@orgasplosion]

Today in my biochemistry lab, my agarose gel did not form properly. When I removed the comb from the gel, it was not solidified enough and so I didn't get my wells to form lol, but this video makes me feel more confident for my next labs! 6 hour labs for the lose

[@kechang9214]

I really like the detail feature in this video.

[@Nhagast]

Um the fire in the background?

[@ThatGuyYouArent2]

Doing this for the first time tomorrow. Hope all goes well! This video has been helpful.

[@JuanOLopezGerena]

This is a very detailed explanation!

[@Onyiiiii]

This was super helpful for my exams today Thank you 💕

[@johnobmasca4304]

Proud to be studying in this fine university😀

[@beecalm3705]

Thank you! Very clear and helpful info

[@casualcasual1234]

when loading the sample to the wells in the gel, do we need to push the micropipette to the second stop?

[@demitriwelling1348]

Excellent video, thanks.

[@lemonade4865]

Good video this deserves many likes

[@Violet_1117]

She has some mad skills 😯

[@Tala_studio]

amazing explanation !!

[@fathimarifai6954]

Well explained 👍

[@Halmont1]

this is amazing i just love it

[@asifdawar9302]

Excellent video..I'm love in it

[@AJ-lo5kf]

I really want to run a gel now

[@lakshminarayanpal4059]

Thnk a lot 🤗

[@alyazan09]

so useful video thank you

[@CatalinaPavezMina]

spiegazione chiarissima veramente bravi posso dire che con questo video sono pronta per il lab di domani :D!

[@arslaankhan8092]

awesome explaination

[@ayaqz3144]

thank you love it

[@foeasy16]

i wish my lab was as clean and sterile as this one

[@Biologyandbiotechnology-qc5jo]

nice lesson

[@zhehanli6689]

6:19 damn bro, ur pushing hard

[@varuno7560]

Where is polymer sheet, DNA probe? You confused me.

[@jub2436]

Nice video! I have a cuestion If I agarose gel 1%,TAE 1Xand small gel How many volts I will use to running the electrophoresis? How long (minutes) is necesary to running the electrophoresis? * I have extracted DNA of 500-700 pb

[@asmaasaad922]

Than you for this informations

[@tahiraghulam2733]

Very interesting..

[@varuno7560]

Why this buffer liquid is added?

[@minabegg1140]

To maintain the required PH.

[@bassamomar4699]

it was really usefull

[@Moonsabie]

i like the errors

[@MickBReedy]

awesome

[@KaiusKing]

Good Video

[@ShadyAgri]

Great

[@TheCatsMe00w]

We just ignoring the unattended bunsen burner in the back huh

[@IanMalcolm99]

i feel sorry for the error guy

[@DizzyDan12]

Dr. Suni brought me here

[@courtneybenavides7998]

do you know what questions she is talking about? i didnt see any questions on tracs

[@DizzyDan12]

The link to the questions is under the video links

[@maham5856]

Video is Good, but here is gona few addition to this 1) dont touch the GelDoc With gloves that we perior already had taken the gell, coz Gell contain ETHIDIUM BROMIDE

[@siddharthsrivastava8652]

Video on calculations that go into making such gel kzbin.info/www/bejne/kF6QmoqgltSXo9E

[@buhariabdullahi3128]

PCR machine

[@TheNatenigga]

bioc2000

[@NocriZle]

exiting jk good vid

[@nothinghereyet1803]

..........

[@falblinger7015]

duh duuuuuu

[@zhehanli6689]

title should be changed to "How Not To Run an Agarose Gel - University of Leicester"