The Principle of Agarose Gel Electrophoresis, a full explanatory video

This video is a full and clear explanation about the principle and the applications of agarose gel electrophoresis.

[@joan-b-empire576]

Love from Cameroon 🇨🇲 thank you

[@romelsoyza4160]

A complete and very easy to understand explanation (like the videos for Flow Cytometry and FACS) on the principles behind the technique.

[@AyazSamo]

She is great a great teacher! Respects from Sindh!

[@mohammedholba2498]

One of the best youtube chanel l ever seen. :)

[@gilyasungi4572]

Well explained! Good explanations linked with real life applications.

[@RohitPant04]

Concise & informative! Good job. 🙏

[@walrus4248]

Fantastic, I learned a lot and I didn't know anything about the subject.

[@mohammedal-hammadi5085]

Wow, this video is so clear and useful, besides you are awesome, thank you so much

[@VarshiiiPrem]

A great teacher..... Thanks a lot... Tomorrow is my exam... Very useful

[@abdulmunafisalisuumar7016]

thank you so much maam, for your wonderful explanation of Principle of Agarose gel electrophoresis.

[@walrus4248]

Will see if you already did capillary electrophoresis, this was such a fine explanation thanks.

[@ridzwanfauzi975]

great video!!really helped me in my test..thank you so much

[@mohanndri64]

Such a good and simply way of explanation thank you

[@tiaxi6779]

very informative video, explained in detail for the reason of each step.

[@muhammadjaber2272]

Your voice like best for presenting and I have get many from your channel

[@ciao_abhi]

This helped me so much for my mcat test

[@maggiejameel6725]

Very well explained, you are an awesome teacher. I SUBSCRIBED

[@sanskrutiraj8051]

This video is very helpful for me. Thank you u explained in easy way 🙂

[@worldaviation4k]

so this isn't used to be able to look at the dna letters? Thanks I've had trouble trying to find the videos where you take the dna and look at the actual proteins. maybe i will find it soon :)

[@qamarhennawi9137]

You are the best, no one like you

[@stephaniehurtado4096]

Late to the upload but I’ve watch almost all your video and they all been so helpful:) ofc ill like and subscribe!

[@poetrylover5561]

You've nicely explained the topic. Many thanks for sharing ♥️

[@sukanyahembrom6213]

very well explained.... thanx alot for making such video

[@ladushky1]

Thank you! we have never add the colour right into the gel tho.. but we do add it to the samples we are running on the gel.

[@user-ff9vu8ic7b]

بجد احسن حد شرح الموضوع دة بالتوفيق❤

[@dstan16224]

Thank you very much ma'am.It really helped a lot.

[@Gbemi78]

your explanation is second to none.

[@Animelover7948]

Very very well explained...very helpful....people out there can try watching this vid

[@trona2612]

Hi Ma'am, thank you very much for such a good,short & crisp but very much informative video on agarose gel electrophoresis.... I've a question on the differential mobility profile of nicked & linear DNA molecules of same size; why do linear DNA molecule migrates ahead of nicked one? I'll will be grateful to hear from you. Thank you!

[@krisantinimarkam3396]

Very well explained and easy to understand. Thank you

[@rahmanebrahimzadegan7198]

You teach excellent. Thank you.

[@bahahos7426]

Thank u very much i love all your videos

[@Amar45611]

Thank you Ma'am.. It's a great video! ❤

[@girlschannel11]

Really good explanation !!!!

[@srigayathri5980]

Thank you so muck mam.Because of u i can able to understand the concept now mam.

[@Min-gh1jr]

Hi this video is great! I was wondering if the thickness of the band would suggest any properties about the nucleic acid strand, i.e there are more nucleic acid fragments of that size?

[@yennguyen-tp7ce]

everything is just so clear, thanks

[@ikhinerawlings124]

Well explained. Thanks. Can talk on chromatography in details

[@Katherine-mf9wz]

Nice job!

[@wonderakpese1901]

Concept well explained. Thank you

[@soheilaazam799]

You are the best molec teacher, who I have ever seen!!! Well done 👍😊 and thanks for the Videos. What is your name by the way???

[@tanimaferdous50]

Very very good explanation

[@setarehsohail5422]

It was a very nice lecture!

[@bharathkumart6097]

Thank you very much for this video ma'am

[@tinyikonkuna1479]

😊😊😊😊Love it here plz make more videos on biology concepts especially 4 varsity students

[@pritichristian2673]

Thanks. Very clear explanation

[@yamaatomayi4315]

mem i like your explanation, i love to hear u r voice again and again u r a great talent .. and i really love..

[@briang1310]

why do indian people always says mem or ma'am

[@SandeepKumar-dd3ie]

@@briang1310 coz it is taught and its logical as well to respect the efforts

[@gabecalderon2043]

@@SandeepKumar-dd3ie learn respect then

[@fasilutubechannel6697]

thanks i hope another video release in this related video

[@sahewa100]

Very well explained.... thanx alot for making such video. This helped a lot in my thesis research. Please continue to teach us :))

[@biomedicalandbiologicalsci4989]

Thank you for your support :)

[@halafr5861]

You are the best thank you from my heart 💜

[@statusboys4036]

God give me an opportunity to spend 15 mins of my life time in a precious way...

[@iliyamohd8154]

Very good presentation

[@jyothinandakumar6190]

Very well explained

[@shailendrayadav5799]

You are great teacher mam

[@insanhabib4497]

Thanks a lot, ma'am.

[@robinkhan6419]

Well presentation

[@dikshashreedevi4568]

please make some more videos .good explanation

[@felixjohnpaulbarqueros6675]

Hi how can I determine the effectiveness if i will alternative coloring dye for the loading buffer

[@stevemorton3078]

Are PCR and then AGE being done in an automated fashion on a single sample in a miniature electrochemical device, such as one that can only be used once ?

[@saraabdulaziz3764]

Very informative🥰

[@krishnanandh7999]

Supr class. Thank you🤩🤩

[@Az-xr5yx]

Thanx thats was helpfull

[@jiaflair]

THANKYOU 💞

[@claudiaaurie8161]

Hi! I just found you and I have been watching your videos. They are amazing! I was wondering (this may be a silly question) but how do you know which restriction enzymes to use for example for paternity testing? does it matter which to use as long as all DNA samples are treated the same? thank you! look forward to watching all your videos--Claudia

[@biomedicalandbiologicalsci4989]

Hei .. thank you for your comment ... as you said, you should treat all the samples with the same restriction enzyme .. and experimentation will show us which is the best restriction enzyme to use :)

[@sidratulmuntaha1687]

@@biomedicalandbiologicalsci4989 Can we search it out from the literature which endonuclease to be used?

[@thnxm8]

Thanks a lot

[@Milahh.]

Thx, very useful well done

[@biomedicalandbiologicalsci4989]

Thank you for your comment ...

[@geeswags6172]

Informative

[@jaswantnegi4879]

Please upload some videos about difference between RNA and DNA isolation and separation techniques. Do tell about Difference in their agarose gel concentration and gel separating chamber, where we use horizontal or vertical gel chambers...

[@nextagro]

Not sure if the comments are still answered, but... Why do we need a PLATINUM wire electrode in the electrophoresis setup? What exactly will happen if one replaces that electrode with an ordinary Copper wire?

[@joyeke6340]

Thank you

[@ranaaamiraamir3437]

Brilliant

[@samanthabautista1655]

Hi im just wondering which buffer to use when your stain is acidic? Because according to a journal ive read that stain that we are about to use when expsed to basic enviroment it can affect the staining capability in a bad way? So which buffers to use??? Anyone can answer? It would help me a lot for our research please

[@lincolnkarim1]

This is not my field at all so please excuse my ignorance; Since DNA is a negative molecule (3:48), does that mean it is an ion?

[@MaryGraceBayot]

Thanks

[@kuldeepdinkar4918]

What is the use of nylon fiber?

[@stevanstankovic8021]

Great video, thanks! I have a question concerning visualisation: If after the gel we have the blue bands with the loadind dye, why do we need to add Ethidium bromide to make it visible under UV? Isn't the information we have from the blue bands sufficient? Or is it maybe, that the blue bands we see after we ran the gel is maybe almost only the dye itself, as it leaves the DNA (or RNA) and just sinks faster to the + side, so that our actual DNA (or RNA) is located a bit above the dye - and that is why we need to check it under UV, as it would be "invisibly" located above the dye? Really can't find any answer to this! Thanks again! (:

[@ladushky1]

We either add GelRed right into the gel or we use ethidium bromide later for visualization; both are carcinogens but we would not use both at the same time.

[@drgaikwadsir7270]

Make some videos related with r dDNA technology

[@emanwanli7740]

I have a question .. when migrating the genomic DNA .. shouldn't multiple bandits appear, each expressing a single chromosome content .. since chromosomes carry DNA of very different sizes, especially if we are talking about humans, for example

[@devyaniitware2428]

What are amplicons?

[@drgaikwadsir7270]

Nice mam

[@jthomas0007]

Hi ma'am, could you please talk about PCR and it's various types?

[@redeemerbadagbor1673]

you do all :salut

[@urmilahussainpiya6735]

please make a vedio why Taq DNA polymerase is thermostable

[@Art-cq1zy]

Im confused. Why does the solution not evaporate in the microwave?

[@Zeenatullah347]

❤❤❤

[@youcare6415]

Very informative. I guess it is SYBR Green not cyber green ;)

[@anirbanhait5998]

Ma'am have pronounced rightly.

[@SLNmin]

It is SYBR, pronounced as cyber but correct spelling is SYBR.

[@wycliffenyandika9017]

like it

[@sukantamandal8106]

Replication

[@jsvclubdeciencia6283]

In silico: kzbin.info/www/bejne/eJy3g4yDn96UqqM

[@blackseastorm61]

I don't think anything in nature and universe is junk or useless

[@ladushky1]

Sorry, but there is no such thing as DNA junk sequence anymore.

[@nagendrag7562]

explained very nicely

[@abeerm9786]

Thank you

[@samanthabautista1655]

Hi im just wondering which buffer to use when your stain is acidic? Because according to a journal ive read that stain that we are about to use when expsed to basic enviroment it can affect the staining capability in a bad way? So which buffers to use??? Anyone can answer? It would help me a lot for our research please