I was so confused with these terms and you explained so clearly and so well. Thank you so much

Thank you soooo much for this. This thing was more like rocket science to me before watching this video. Cleared all the concepts in just one go. Thanks again. 😊 Have great day ahead

Merci pour la vidéo, elle est très claire et parfaite pour bien comprendre le mécanisme de la retrotransciption ! Thank you !

Sehr verständlich, vielen Dank!

Thank You So much Sir.. I watched lot of Videos But No one explained about RNaseH Function and I was really confused. You Really Explained very nicely. Thanks for making this video..

Thank u so much. before I watch this video I read some what notes but they were boring. ur video were so interesting with smooth sound and full information.

Thank you we need more explanation in different Lab techniques. It is practical and we know need to know the sciences. Most of the time I find myself confused in class but thanks to you now I understand it better. Keep it up we need you. You deserve all the success.

Excellent explanation & graphics. Keep up the good work!

This is great. Perfect rythm. Thank you.

Very helpful! I finally understand what do we actually use reverse transcription for, thank you!

Thank you so much, Sir! the explanation is to be so clear and easy to understand for us.

My doctor should watch this srsly

Excellent video. You made this concept easy to understand, thank you.

@henrikslab

2 жыл бұрын

Embrace tranquility. Thanks, Zen

Fantastic! Amazing! Incredible! Astounding! Mighty! Wonder! Super!

@henrikslab

2 жыл бұрын

Wow

Thank you so much. The explanation is very intelligible.

Sir I have lack of word to thanks you. Really you I m very excited after watched this . Stay bless forever God bless you More and more forever ❣️💝

Very good explanation man. Thank you so much!

Excellent explanation!

Very well explained concepts are clear about cdna

Thanks you so much finally got what i was looking for

i was confused for intron thingy and u made it easy

This helped me with my genomics class 🔥🤙🏿

Thank you so much Henrik's Lab. You are doing a very noble job by providing us such useful concept clearing video. Through your videos we are able to understand the topic better than hours of classroom learning. ❤❤

@henrikslab

2 жыл бұрын

Very pleased to read that! Thanks ❤

@rajmangalpandey3910

6 ай бұрын

At 2:02 , that mrna and dna combination could contain all 5 types of nucleotide, A,T,G,C,U?

@Abhinav-kf4wd

6 ай бұрын

Yes ​@@rajmangalpandey3910 you are right. The mRNA-cDNA hybrid so produced contains all 5 bases. Please also note that only the template mRNA strand contains Uracil. The two enzymes used here are: (1) RNA dependent DNA polymerase (reverse transcriptase) and (2) DNA dependent DNA polymerase (DNA polymerase 1) These enzymes used here cannot add uracil during polymerization, therefore uracil will be absent in the newly synthesized DNA strands.

@rajmangalpandey3910

6 ай бұрын

@@Abhinav-kf4wd why Rnase didn't ate whole RNA? But made small fragments

@Abhinav-kf4wd

6 ай бұрын

​@@rajmangalpandey3910 I do not know the reason. But If RNase H hydrolyzed the entire mRNA strand then there would be no primer left for DNA polymerase 1 to act.

Amazing! Thanks!

Great explanation!

Keep up the good work

Muy buen video! Gracias!

thank you very very much!

Best video ever❤️❤️

amazing explanation. cheers mate

Thank you 😊💕💕

Muito bom o vídeo, parabéns 👏🏽👏🏽👏🏽💚

Thank you so much sir❤

Thank you very much..

Thank you so much!

amazing , keep going

Thank you ❤ God bless you ❤️

🙏thank you.

it is very nice and please adding brief explanation about recombinant DNA

Nice explanation ❤️

Thanks!!!!

Thank you

How do you make cohesive ends on the cDNA so you can be able to ligate it with the chosen vector?(using restriction enzymes for the cDNA given would cut out some of the coding sequence right? so how do you add cohesive ends? thanks

Hi, i hope someone will help you the way u helped me today, I wish u the best from France

Thanks :)

Danke, brudi! Arbeiten grade an einer präsi über Gen Chips und das ist verdammt nützlich!!! Love you

At 3:20 the last exon shouldn't have blue "legs", because blue was polyA before. Poly A is not in DNA.

Hey, one question after the synthesis of ds-cDNA. How it will multiply in numbers.................Without having the primer for coding another strand....?

Today, my Professor explained this topic to us, somehow she explained, that after the synthesis of the first cDNA-Strand the Double-Strand would be denaturated into Two seperate ones, later there are inhibitors to Stopp the accurance of Rnase. Later Taq-Polymerase is Synthesizing the other Strand from the cDNA-Strand that was reverse trnascripted before, not like in your video by Nicking from the Rnase and Polymerase 1 and later with Ligase. I asked her about this and she thought that you explained it as an example how it would happen in the body not like in Biotechnology. Im got super confused that she explained it different at some point. Weirdly enough she suggested us your video to learn the reverse transkription, thats why i confronted her today, in order to get clear what is correct for her exam XD Maybe the is some potential to make a different video out of it? Danke für das gute Video. Hab es dennoch gut verstehen können!

@henrikslab

Жыл бұрын

Hey, thanks for this message! I created this video based on the following nature paper: www.nature.com/articles/nmeth0205-151 Here, it also includes the nicks. But as alwayas: there is not only one protocol or kit. There are a few ways to generate cDNA. Hope it helps a little!

Hello, i am facing problem in cdna synthesis. would you please help me to know your protocol?

Is there no hairpin loop?

Mam 5'AGUCAGGUC3' this is mrna what is the C dna to this sequence

Thank you. How can we contact you if we get problem while doing qpcr wirk?

@henrikslab

3 жыл бұрын

Either here or in the comment section of the qPCR video

@user-mm8cq9xg3m

3 жыл бұрын

Thank you for your quick response. Do you have some vedios for analyzing the data of qPCR?

@henrikslab

3 жыл бұрын

@@user-mm8cq9xg3m not for data analysis yet.. but I indeed consider to do one (end of April)

in 2:57 may I ask how whole mrna are replaced by the DNA? thank you

@sanidhyapai7919

3 жыл бұрын

I think, the same exonuclease activity will remove the rest of the RNA parts

Why cant we use mRNA directly in microarray or qPCR

@Joeythegoats

2 жыл бұрын

it wont express completely to give information. we must use reverse transcriptase, bcos hybridization will only occur when we will use cDNA due to presence of oligo sequences on microarray.

Is there a way we could translate all the proteins in a human genome and create a lab created human since the entire genome has been sequenced?

@henrikslab

3 жыл бұрын

Hope I got your point (create a completely synthetic human with proteins that we put in cells)? Very interesting idea. I know that something like this was done already with bacteria... but for mammals this would be way more difficult. Image, there are more things than protein.. regulatory RNAs, the DNA itself is required.. there is methylation (some genes are inactivated and some others activated). So there are more components than protein, but extremely interesting to follow up on this in a smaller way!

Wow! what can I get you from the vending machine

😃😃

I have a question. What´s the meaning of the last product in this process? what is "ds"?

@henrikslab

Жыл бұрын

Thanks for asking! dsDNA = double stranded DNA

@donovanvargasalcantar2534

Жыл бұрын

@@henrikslab Thanks for supported me! Your video is all that i needed to understand this process. SUPER LIKE :)

Can you Translation.. to Arabic

Bist du deutscher ? So hörst du dich an XD

deutsch wär echt cooler gewesen

Wait a second people...forgive my lack of understanding but i dont understand why start to syntettize anything about and HUMAN DNA??? Why want to know what GOD did once and why and how and how to REVERSE IT/////?????!! Please someone explain..Many thanks

@sissisophie3303

Жыл бұрын

Only virus can do that

@critikasalihmeylani

7 ай бұрын

We can do literally anything by manipulating our genes. Ofcourse, to do so, one needs to know how to speak the language of life; the language of proteins. Our genes controls our everything. You can be eternally healthy, have a perfect immune system, become a superpowered human, have 200 IQ, be able to photosynthesize, and literally become biologically equivalent of immortal. We reverse it to recreate it, and improve it.

@doctorposting

5 ай бұрын

🤣🤣🤣🤣

Bruder sprich doch deutsch

Man trying to play God not our place to mess with God's code that makes us human.

@laecatara1

2 жыл бұрын

I've been reading about the cDna lately after the vakka vakka I can't quite decipher it yet kzread.info/dash/bejne/hHWNvNaRfajVp9I.html Just look for the explanation I come across this cDNA when someone takes the Weuka Woeka

@cheyennes654

2 жыл бұрын

As in the days of Noah !!! Praise the Lord !!!

@AA-gl1dr

Жыл бұрын

Did you know that RNA isn’t just a human thing?

@Jesus_is_Good_God

6 ай бұрын

We use this process for a very useful purpose at our citrus pathology lab. It helps us to see if our treatments against a particular pathogen are useful or not.

@anthonyhernandez3546

6 ай бұрын

Shut up you talk to the sky like a crazy person