Accelerating the pace of genomics
1:44
xGen™ for Element Biosciences
0:36
CRISPR knock-in: Tips and tricks
7:09
Пікірлер
@philp1232
@philp1232 15 күн бұрын
An Awesome super informative presentation thank you!
@llsa2009
@llsa2009 2 ай бұрын
I am wondering if you have automation solutions for xGen cfDNA&FFPE Lib Prep?
@idtdnabio
@idtdnabio 2 ай бұрын
Yes, we do. We offer several automation solutions for the xGen cfDNA & FFPE Lib Prep Kits. Learn more with the link below about which platforms support xGen NGS and let us know if you have any additional questions: www.idtdna.com/pages/landing/ngs-automation
@dongphucau8432
@dongphucau8432 2 ай бұрын
Hi, can you have me to select cells being knocked-in (point mutation)
@marshallfritz6361
@marshallfritz6361 3 ай бұрын
Was this supposed to be informative, or is it just to troll anyone who hits the help button?
@idtdnabio
@idtdnabio 3 ай бұрын
Thank you for your comment. This page: www.idtdna.com/pages/support/how-to-order may be more helpful, as well as our FAQs page: www.idtdna.com/pages/support/faqs
@KyleKings2002
@KyleKings2002 5 ай бұрын
Do you know any more about a disorder carded by damaged chromosomes #3, and #7?
@KyleKings2002
@KyleKings2002 5 ай бұрын
Do you know any more about a disorder carded by damaged chromosomes #3, and #7?
@user-yu4rg8be6x
@user-yu4rg8be6x 6 ай бұрын
Is it acidic, for the crystalline prosses to take place .say to be used to up load memory. And or knowledge ext
@aymankhalifa5462
@aymankhalifa5462 7 ай бұрын
Thank you so much!
@bogonkobenardnyakundinyaku7852
@bogonkobenardnyakundinyaku7852 7 ай бұрын
This is very informative. You have answered most of the questions I had and enlightened me immensely
@George-rq1yp
@George-rq1yp 10 ай бұрын
Very thorough presenter, good job!
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Loves
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Very nice video
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Loves
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
nice video dear
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Excellent video
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Loves video
@LivaEntertainment-nd1sg
@LivaEntertainment-nd1sg 11 ай бұрын
Very nice video
@marwanhesham7407
@marwanhesham7407 11 ай бұрын
Thank you! So informative.
@winfred4193
@winfred4193 Жыл бұрын
*Promo sm* 🏃
@aldhairmedico9408
@aldhairmedico9408 Жыл бұрын
Is xGen Exome Hyb Panel the same as xGen Exome Research Panel?
@georgiabailey1374
@georgiabailey1374 Жыл бұрын
Is this free?
@floridakenoly4849
@floridakenoly4849 Жыл бұрын
I was able to beat my genital herpes after the use of Dr UGBOKHOLAN herbal medication am a living testimony
@terrylai1532
@terrylai1532 Жыл бұрын
Hi, does the PrimerQuest tool design primers at exons only? (exon-exon junction primers), or it just randomly generates primers? "Without changing any setting..etc"
@abdulrahamandanlami6897
@abdulrahamandanlami6897 2 жыл бұрын
Thank you for being the dedicated, thoughtful, and compassionate doctor that you are, you are more honest than I imagined, thank you so much Dr Igudia KZfaq channel for curing my genital herpes, you are amazing
@anndiamond7601
@anndiamond7601 2 жыл бұрын
Thank you so much, this is very helpful ! 🙏🌸💐
@cacevedo07
@cacevedo07 2 жыл бұрын
Very clear and well-explained information. Many thanks.
@azukarzuchastux8066
@azukarzuchastux8066 2 жыл бұрын
John 3:16 KJV For God so loved the world, that he gave his only begotten Son, that whosoever believeth in him should not perish, but have everlasting life.
@kakhangchungpanmei8205
@kakhangchungpanmei8205 2 жыл бұрын
Really really good and important presentation.
@thavamanirajapandi2505
@thavamanirajapandi2505 2 жыл бұрын
Great presentation!
@phucle6961
@phucle6961 2 жыл бұрын
You try to give the video more brightness it will be great if you do
@tD-wp5vj
@tD-wp5vj 3 жыл бұрын
thanks for the video very enlightening
@OneRoadLeadsToYah
@OneRoadLeadsToYah 3 жыл бұрын
Great presentation thank you Dr. Bustin!
@nola-baissa2433
@nola-baissa2433 3 жыл бұрын
Unfortunately this is very hard to understand and even the subtitles are incomprehensible...
@asliss07
@asliss07 3 жыл бұрын
Hello, I woulg like to design a probe following the primers I already have, but when I visit the website they ask me to log in, I need to create an account for do it?
@idtdnabio
@idtdnabio 3 жыл бұрын
Hi Astrid. Send us an email at [email protected]
@edyoucate1774
@edyoucate1774 3 жыл бұрын
Wow nice video, thanks for helping me understand this topic
@nathannobbe6113
@nathannobbe6113 3 жыл бұрын
Great work Randy; your contributions to society have been and will continue to be profound!
@knrdx8848
@knrdx8848 3 жыл бұрын
Hey, nice videos. I have a question. Do you know how to make a deletion of the yeast X gene and expression of the X human gene while using yeast strain W303?
@idtdnabio
@idtdnabio 3 жыл бұрын
Thank you for your question! While IDT does not have specific methods for deletion and expression of genes in yeast, we do offer a number of resources for CRISPR editing and homology-directed repair (HDR) that can be used for deletion or insertion of targets of interest. The following page is a good starting point: www.idtdna.com/pages/promotions/crispr-hdr-design-tool-and-donor-oligos and includes a link to IDT's Alt-R HDR Design tool. Please feel free to reach out to our Application Support team ([email protected]) with any further questions!
@anndiamond7601
@anndiamond7601 3 жыл бұрын
Thank you very much for the presentation. It's very helpful and interesting.
@anndiamond7601
@anndiamond7601 3 жыл бұрын
I'm so thankful for your presentation, it's really helpful. Further updates on this topic will be greatly appreciated. Thank you.
@sbmabusaeedranashahriar7399
@sbmabusaeedranashahriar7399 3 жыл бұрын
🤝
@faezamokranenaitmohamed8788
@faezamokranenaitmohamed8788 3 жыл бұрын
excellent, very well explained. thank you
@luv9765
@luv9765 3 жыл бұрын
could you share the design tools that you used to generate ASO sequences? Thank you!
@idtdnabio
@idtdnabio 3 жыл бұрын
Hi Yunyi!. Thanks for your comment. We'd be happy to assist if you're looking for ASO design advice. Just email us at [email protected]. Thanks.
@sahelipramanik6215
@sahelipramanik6215 Жыл бұрын
@@idtdnabio how can I design ASO for lncRNA in idt?
@milena9386
@milena9386 3 жыл бұрын
Great video
@114penandsword4
@114penandsword4 3 жыл бұрын
penandsword.hatenablog.com/entry/2020/12/19/160123
@mamankhyam3385
@mamankhyam3385 3 жыл бұрын
Hi I need to know that how to save primers sequence after making primers from "Pre-design qPCR library"?
@deborahsimons2837
@deborahsimons2837 3 жыл бұрын
I Can't still believe that i got cured from Genital Herpes through herbal treatment from Dr Lucky Aduku who I met on the internet, I actually couldn't believe it at first because it sounded impossible to me knowing how far I have gone just to get rid of it. Dr Lucky Aduku send me his medicine which I took as instructed and here I am living a happy life once again, a big thanks to Dr Lucky Aduku, I am sure there are many herbal doctors out there but Dr Lucky Aduku did it for me, contact him [email protected] , also call or whatsApp him on +2347017652474..
@behnazoujand2938
@behnazoujand2938 3 жыл бұрын
Is this suitable for degenerate primer design?
@kaBHROMixVlog
@kaBHROMixVlog 3 жыл бұрын
Thanks for sharing searcher929
@yannfrey
@yannfrey 4 жыл бұрын
Thanks, very clear and informative!
@dr.fredrickkizitophd1339
@dr.fredrickkizitophd1339 4 жыл бұрын
Our wish is that you share your protocol for siRNA online the way other companies like Invitrogen do, so that when we buy your products, it is easy to use an online protocol for reconstitution. You can also make a video on this. Otherwise, we buy your products but your protocols are not easy to find. You normally tell us to go to www.idtdna.com, etc but we don't see the things there. Please share you reconstitution protocols for the siRNAs.
@dkumar4024
@dkumar4024 2 жыл бұрын
very true said!!