This channel is underrated... It needs recognition
@LucasLearnzКүн бұрын
That is so nice of you! I honestly feel super grateful for all of the recognition I already get!
@rios_music.hub__2 күн бұрын
How joyful learning is thiss... Just enjoyed 🤍💯
@LucasLearnz2 күн бұрын
That's wonderful to hear! Thank you!
@juileeparpart793 күн бұрын
This was SOOOOO helpful. Concise and easy to follow. Thank you!
@LucasLearnz2 күн бұрын
I'm really happy to hear that! I'll try to make more videos soon just like it!
@adityachowdhury83246 күн бұрын
Very much helpful for interviews as well! Thank you! Love from India❤
@LucasLearnz2 күн бұрын
That's fantastic to hear! I hope your interview went well!
@osagieprecious82828 күн бұрын
Watching 2 hours before exam
@LucasLearnz2 күн бұрын
Good luck on your exam!
@sarahegazy90568 күн бұрын
Thanks alot very useful explanation
@LucasLearnz2 күн бұрын
Glad it was helpful!
@user-fv8tj8sb7j9 күн бұрын
How about the od600 in microorganism? It seems like they don't use ''absorb'' the light, they use ''scattered''. So it means the more microorganism in the suspension the more light will scattered, and the detector will detect less light. So absorbance will increase? Besides, why use 600nm to measure microorganism, is there some specific reason?
@Reeeeper9 күн бұрын
awesome and really simplified
@LucasLearnz2 күн бұрын
Great to hear!
@rushikeshugaonkar62679 күн бұрын
17/3 is 5.67
@LucasLearnz9 күн бұрын
Sorry about that🙈😅
@priyaselvam7649 күн бұрын
Kindly share your mail id...have queries
@derpywoodoo11 күн бұрын
Honestly, just using this to brush up on college chemistry classes was very nice. Thank you!
@LucasLearnz11 күн бұрын
That's great to hear! Thank you!!🙏
@Fabian-nh3yf15 күн бұрын
Bacteriophages can't express genes, it's the hosts that do it for them. Very important distinction in my opinion.
@LucasLearnz15 күн бұрын
@@Fabian-nh3yf Absolutely! I apologize if that wasn't made clear in the video!
@chikaokolo492917 күн бұрын
Excellent explanation
@LucasLearnz17 күн бұрын
@@chikaokolo4929 Thank you!
@JimBobe18 күн бұрын
Please drink some water next time. The lip smacking noise is so annoying
@LucasLearnz17 күн бұрын
Thanks for the feedback! I'll try to stop that in the future😂👍
@JimKhan-r5b18 күн бұрын
Miller Ruth Lopez Richard Martinez Donna
@HasnaHafida-j1m22 күн бұрын
So helpful, thanks!
@LucasLearnz22 күн бұрын
Happy I could help!😇♥️
@rawanehab345423 күн бұрын
i love u please dont die
@LucasLearnz23 күн бұрын
Hahaha, thank you but I don't think you'll have to worry about that just yet😇
@PedroBaker-b5d23 күн бұрын
Martinez George Martinez Patricia Johnson Nancy
@leandrosantorsola68425 күн бұрын
Thanks!
@LucasLearnz25 күн бұрын
@@leandrosantorsola684 Happy I could help!😇👍
@Carles-s9c26 күн бұрын
Great video, but buy a pop filter for next videos please
@LucasLearnz26 күн бұрын
@@Carles-s9c This one is old and I have done so now👍
@MeganBradshaw-du2tf27 күн бұрын
Can you please make a video on the different types of microscopes too, please? Preferably before 20th (that's when I have my exam) you can explain, the bright field, dark field, TEM AND SEM, cryo electron and atomic force electron. (Ps counting on you) 🤍,
@LucasLearnz27 күн бұрын
@@MeganBradshaw-du2tf sorry to let you down but I'm not familiar with the field so sadly I won't get such a video out in just 4 days😟 Best of luck to you!!
@MeganBradshaw-du2tf26 күн бұрын
@@LucasLearnz Thanks anyway!! and keep up the good work. God bless
@LucasLearnz26 күн бұрын
@@MeganBradshaw-du2tf Thank you!
@AngelicaLLamas-pt4dz27 күн бұрын
Is this the same as mesotherapy?
@ahaf4654Ай бұрын
When you say "net charge of the field", is that determined using the RF to DC ratio?
@ibshelby3643Ай бұрын
good video but not long enough
@LucasLearnzАй бұрын
I try to make them as short as I scan but that sadly sacrifices some depth. I'm sorry about that but it's still how I feel I can serve the best!
@ibshelby3643Ай бұрын
@@LucasLearnz no still thank you , sorry for my tone was harsh
@LucasLearnzАй бұрын
@@ibshelby3643 Oh don't worry, I didn't it was. If anything I took your comment as a compliment since it implied you wanted more!😇
Great to hear that you appreciate it! I do my utmost to make learning easy and FAST!
@Biologyandbiotechnology-qc5joАй бұрын
kzbin.info/door/QJxWqJKndee2n3TaljBjIQ
@asbaDoceАй бұрын
How come you are the very same graphic as Prof Daniel? kzbin.info/www/bejne/sKa4p4SEbbCLhc0 are you using a textbook?
@LucasLearnzАй бұрын
It's one of the easily available images on the web that fall under Creative Commons, meaning that anyone can use them for a video😇
@ramgopalnirmalkar190Ай бұрын
Nice explanation
@LucasLearnzАй бұрын
Thank you!
@AM1381.5Ай бұрын
The link for ShortChemistry is not working. I found it on a different link: kzbin.info/www/bejne/rKavo6Cdoq9oaqc
@LucasLearnzАй бұрын
Thank you for letting me know!🙏
@soggyboogyАй бұрын
Quality content under 3 minutes😮, this video is amazing for my last minute revision, thanks❤
@LucasLearnzАй бұрын
That's fantastic to hear!🔥
@adamfeinstein2764Ай бұрын
I think the basic emojis and simple cartoons are great for learning and understanding! I noticed that you said RNA Polymerase codes from the 3'--> 5' direction (1:01) when I believe it is the other way around. other than that, I really enjoyed the video!! Keep it up!!!
Hey Lucas, any chance you could make a vid on first and second order kinetics? Your format is super friendly and easy to learn with compared to other creators.
@LucasLearnz2 күн бұрын
Hi! I'll add it to my todo list but for right now I'm doing almost all of my videos on Google Sheets as it relates better to my day job.
@MaryamFarooq-lp2khАй бұрын
Amazing lecture Just love the teaching style❤ Really helpful😊
@AdamSG12122 ай бұрын
Variable region not the constant region
@bogdanator8752 ай бұрын
Your illustrations are wrong. The antigen is not bound at the Fc part but instead at the Fab. Your antibodies are inverted
@LucasLearnz2 ай бұрын
Thanks for notifying me!
@bogdanator875Ай бұрын
@@LucasLearnz You´re welcome! Aside from that little error I really liked your video 👍
@bonerickabaga69552 ай бұрын
is class 1 type also called as replicative and class 2 as non replicative?
@user-oi2dw5wq4w2 ай бұрын
Thanks a lot that was clear and useful
@LucasLearnz2 ай бұрын
I'm happy to hear that😇👍
@edreesamani22942 ай бұрын
Hello this was a great video explaining how MALDI-TOF works! I am currently using the MALDI-TOF on some peptides I'm making and I had a question. The peptides we are making has a +4 net charge but on the maldi we usually see +1 charge mass (m/z) on the spectra and not the +4 charged (m/z) mass. Can you explain this? Thank you!
@LucasLearnz2 ай бұрын
How does that show up exactly? I mean how do you know that you're seeing +1 charge rather than +4 charge?🤔 I've only analyzed things that had a +1 charge myself I'm afraid🙈😅
@edreesamani22942 ай бұрын
@@LucasLearnz Hi thanks for responding! I know that it is the +1 charge because that is the predicted mass of my peptide. My peptide has a mass of 1154 g/mol and that is the peak that I see on the maldi-tof. I am just confused because the peptide has charged amino acid residues that should be fully protonated with a net +4 charge when it is on the plate with the matrix.
@777swampie2 ай бұрын
The biggest problem with GC-MS is the companies producing them will not compete to drive the price down. We need more research which means lower analytical equipment costs. Everybody who wants to do research can't just happen to get a job with a deep pockets corporation supporting their work. To advance science...lower the tool costs!
@LucasLearnz2 ай бұрын
I couldn't agree more! However I'm sure some of that cost comes from the fact that these instruments are not exactly cheap to manufacture. But I agree that it would be fantastic if more affordable options would exist!