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

She is great a great teacher! Respects from Sindh!

Love from Cameroon 🇨🇲 thank you

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

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

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

This helped me so much for my mcat test

Such a good and simply way of explanation thank you

بجد احسن حد شرح الموضوع دة بالتوفيق❤

Well explained! Good explanations linked with real life applications.

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.

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

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

Concise & informative! Good job. 🙏

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

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

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

your explanation is second to none.

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

You teach excellent. Thank you.

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

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

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

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

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

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 :)

Thank u very much i love all your videos

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

Very well explained and easy to understand. Thank you

Really good explanation !!!!

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

Concept well explained. Thank you

You are the best, no one like you

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

Very very good explanation

Thank you very much for this video ma'am

everything is just so clear, thanks

@ikhinerawlings124

Жыл бұрын

Well explained. Thanks. Can talk on chromatography in details

Thanks. Very clear explanation

It was a very nice lecture!

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

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!

You are great teacher mam

You are the best thank you from my heart 💜

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

Thanks a lot, ma'am.

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?

Nice job!

Very well explained

Very good presentation

Supr class. Thank you🤩🤩

Thanx thats was helpfull

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???

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

5 жыл бұрын

why do indian people always says mem or ma'am

@SandeepKumar-dd3ie

4 жыл бұрын

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

@gabecalderon2043

2 жыл бұрын

@@SandeepKumar-dd3ie learn respect then

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

please make some more videos .good explanation

thanks i hope another video release in this related video

Well presentation

THANKYOU 💞

Very informative🥰

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

@biomedicalandbiologicalsci4989

6 жыл бұрын

Thank you for your support :)

Thanks a lot

Thank you

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

Informative

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 ?

Thx, very useful well done

@biomedicalandbiologicalsci4989

7 жыл бұрын

Thank you for your comment ...

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

Brilliant

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...

Thanks

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?

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

6 жыл бұрын

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

5 жыл бұрын

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

What is the use of nylon fiber?

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?

Make some videos related with r dDNA technology

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

please make a vedio why Taq DNA polymerase is thermostable

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

Nice mam

What are amplicons?

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

3 жыл бұрын

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.

you do all :salut

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

@anirbanhait5998

2 жыл бұрын

Ma'am have pronounced rightly.

@SLNmin

Жыл бұрын

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

❤❤❤

like it

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

Replication

In silico: kzread.info/dash/bejne/dJ-ItLuGmtzHpKQ.html

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

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

explained very nicely

Thank you

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