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@susanlu67925 күн бұрын
Thank you very much for providing this excellent video! easy to understand and follow, excellent !
@kotosqoposrly27 күн бұрын
Thanks so SO soooooo much for this!
@hoatzinn3106Ай бұрын
This makes so much more sense now! Thank you for making this video!
@mody_571Ай бұрын
who came after nobel prize announcement?
@pingukuteproАй бұрын
IS THIS A NOT GATE?
@thespringmonster7807Ай бұрын
and this years Nobel Prize went to....
@BiruinThailandАй бұрын
The Nobel Assembly at Karolinska Institutet has today decided to award the 2024 Nobel Prize in Physiology or Medicine jointly to Victor Ambros and Gary Ruvkun for the discovery of microRNA and its role in post-transcriptional gene regulation.
@arsh.7480Ай бұрын
This year Nobel prize is for the discovery of micro RNA
@tek23502 ай бұрын
i tried 5 other videos ..this one was the one
@Googoogaga4433 ай бұрын
Hey why are you not uploading anything anymorr??
@BasicBiochem3 ай бұрын
@@Googoogaga443 What topics would you like me to cover? 😁
@sof89005 ай бұрын
this is the most helpful video I've seen on KZbin, truly thank you!
@TrieuSangVietnam9 ай бұрын
Some times when sequencing on an ion torrent machine, there is a barcode that takes up a lot of data space, causing the sample data to be insufficient for analysis. But still on this Chip sequencing, re-process the chip: wash the chip, then denature again with primer sequencing and wash the chip again and add the sequencing enzyme and then run the sequencing again, then the No barcode is almost reduced. . Is there any way to reduce the No barcode at the beginning of sequencing after loading the denatured sample onto the sequencing chip?
@ashritpattanayakfan11 ай бұрын
Omggggggg i can't thank you enough!!!! I have a major test day after tomorrow and was so confused about the adaptors and emPCR. THIS IS THE BEST VIDEO ON PYROSEQUENCING ! You deserve more views girllll ❤
@BasicBiochem11 ай бұрын
So happy I could help clear things up! Hope your test went well!
@imandjeraoui3067 Жыл бұрын
microrna are they intron or gene endors? Help me
@Rishiz50 Жыл бұрын
Brilliant explanation. Thank you 🙏
@bhanupriyach4287 Жыл бұрын
well animated and explained. Fantastic
@sumaiashetuvlogz6264 Жыл бұрын
You are presenting like you are reading too fast to understand
@ozgurcan7907 Жыл бұрын
After 4 youtube videos that really lacked explaining a lot of the major details, I found this video. Great explanation and annotation. Thank you so much for the work, effort, and knowledge you present to us!
@ianccco4648 Жыл бұрын
Fantastic! Thank you🎉
@sebastiansybertz Жыл бұрын
Thank you very much, there isn't a single German video about this method, but I understood very well.
@lisen8036 Жыл бұрын
this video should have so many more clicks! like I watched every single video on yt about the chain termination method and this was the only one that explained it clearly but enough detailed, great work on this
@abdelrahmanosama2359 Жыл бұрын
This video helped me a lot ,so greatful ❤
@Jeetjemina Жыл бұрын
helpful, ty!
@nathanschot7226 Жыл бұрын
Fantastic video, super clear, easy to follow, great visuals. You could barely even call me a biology student and I still had no problem understanding a technology that would normally be incomprehensible to me 😂
@hawarykurdy3229 Жыл бұрын
really excellent
@sscrunches9416 Жыл бұрын
Im Working in laboratory Where we Doing Only Coivd RNA amplification using ( BIORAD ) to identify whether it is present or not . But Im fully interested To learn molecular techniques. now I am job seeker like Project assistant/Project associate/Junior Research Fellow etc ... Is there any chance get jobs like these in Canada I'm ready but I don't know how to execute if u don't mind help me .
@malotourneur46 Жыл бұрын
Very clear !! Thank you
@OmkarYadav-be7ev Жыл бұрын
Amazing Video!!!! Ma'am Please make a video on sequencing by ligation (SOLID). Thanks a ton!!
@sscrunches9416 Жыл бұрын
Duration 0.13 l have template DNA tha I'm curious to know the sequence Duration 0.30 Primer Annealing My Doubt 1. If want to know the sequence mean u don't know the sequence so u need to know 2. At 0.30 show the primer which attached to the SSDNA. You don't know the seq of your template 🤔🤔🤔then how your primer recognizes it
@lisanovember1679 Жыл бұрын
you can clone the DNA into a vector and design primers (because we know the sequence of the vector) at the beginning and ending of our insert (our unknown DNA). now the polymerase will start at the beginning of our insert and amplify it.
@sscrunches9416 Жыл бұрын
@@lisanovember1679 Thanks For Your Response
@sscrunches9416 Жыл бұрын
I'm Surya Prakash From India 25 yr old I want Your Email ID for my Study purpose ( Good Student )
@animepolar24 Жыл бұрын
Video tuyệt vời
@palamalama Жыл бұрын
Honestly, what a fantastic video. Thanks!
@aybarsds Жыл бұрын
Clear and loud, thanks!
@shashankprasad4227 Жыл бұрын
Thankyou!
@lisaandriani4378 Жыл бұрын
thanks for the simple explanation, really appreciate it.
@purethanwarat37562 жыл бұрын
Thank you very much 🥰🥰
@SA-nu2so2 жыл бұрын
You need to make the part 2 ASAP, I’ve read over 10 journal articles, each made me understand but this is the headache-free version
@bnuuywaltz2 жыл бұрын
Love the clear and memorable way you explain this! This series is really helping me study for my midterm :) thanks a lot!!!!!
@BasicBiochem2 жыл бұрын
Happy to help! Let me know if there’s other topic suggestions that aren’t on KZbin ☺️
@loulashhh92702 жыл бұрын
Thank you so much that was a lot easier to understand!! If you don't mind can u send me the presentation you worked with I'd like to use the figures but I couldn't find them anywhere on the internet...
@courtneyczb2 жыл бұрын
Thank you so much! It's so clear and so aesthetic!!
@ChristianDemirdzhiyan2 жыл бұрын
Amazing video. Thank you so much!
@TrucNguyen-nn8po2 жыл бұрын
❤️❤️❤️
@rubenscherer38042 жыл бұрын
good vid
@layalbdirat6272 жыл бұрын
Excellent video
@ritikasingh88092 жыл бұрын
Helpful
@ritikasingh88092 жыл бұрын
well explained
@explorerjaat95322 жыл бұрын
Thank you! Please keep making videos like this Will lot of people
@brenda.rodriguez20032 жыл бұрын
The way you explain and write notes makes me want to be your study partner!
@rutlevy79822 жыл бұрын
Thanks it was great! But I don't understand how using a capillary gel electrophoresis would help not making separate reaction mixtures. I would love an explanation on that. Thanks again!