How-to create systems in Services Central
1:23
How-to create groups in Services Central
1:17
Innovating for a brighter future
2:50
19 сағат бұрын
Fujifilm Scott Lowrie Presentation
14:38
Пікірлер
@johnk4121
@johnk4121 14 сағат бұрын
Worst description ever.
@JOHNDOE-rr7uo
@JOHNDOE-rr7uo 21 сағат бұрын
You are the best. Thank you very much.
@eduardomorgado1488
@eduardomorgado1488 3 күн бұрын
i hate genetics
@eduardomorgado1488
@eduardomorgado1488 3 күн бұрын
good video tho
@user-en1rm4lb3v
@user-en1rm4lb3v 3 күн бұрын
Can we use this multiple times for same sample. Means I have to concentrate same protein with same buffer after 1 month then can I store this? If yes then how we store it?
@thaotranphuong6626
@thaotranphuong6626 5 күн бұрын
Do you have any video about real-time PCR set up in 7900HT machine? I am driving crazy about this
@potatocats5716
@potatocats5716 6 күн бұрын
Citadel of Void (CoV) is a cancelled,[i][4][5] NilIcon nil difficulty, mixed-progression-based Citadel that was to be located in Emblem Ring1 Ring 1.[6] CoV is a well-known nil difficulty citadel,[b] with a 10-floor ascension section, 4-floor sideways progression, and concluding with an 8-floor descension section. The current version of CoV can be played in its own place here, and the original Tower of Void can be played here.[j] CoV is no longer found in Ring 1, although rarely in the ring select it may appear (please note that despite it rarely appearing in the ring select, it is not available in-game). It was originally meant to be found via solving a series of complex puzzles across The Great Inferno, which required logic and critical thinking skills.[7] The current difficulty range of this citadel's floors ranges from Challenging to nil.[k] This citadel was later split into two halves, nerfed, and added to Pit of Misery as Tower of Eternal Void (Only F1-10 and nerfed to be HorrificIconModified100 Horrific),[l] and Citadel of Infinite Void (Floor 11 onwards, nerfed to UnrealIconModified100 Unreal).
@AmruMagdy
@AmruMagdy 6 күн бұрын
جزاكم الله خيرا 100%😂❤🎉😅
@basantabdulrahman9346
@basantabdulrahman9346 9 күн бұрын
thank you, that very helpful
@user-hl2iy2uq1b
@user-hl2iy2uq1b 9 күн бұрын
請問有講義嗎
@vishalchaudhary3651
@vishalchaudhary3651 9 күн бұрын
Bhaiya ma india sa hu mujhko spinal cord injury hui h 7 years ho gye c7 asia-B plz aap ya batao mujhe stem cell sa thik ho sakta hu plz help me bhaiya 😢😢
@blandon93
@blandon93 9 күн бұрын
Which metal do you use? What separates DNA from the metal ions? Is DNA-Metal salt solutable? Some proteins have negative charge and they might take the spot on the beads.
@denshin-5640
@denshin-5640 10 күн бұрын
Wow, your son has the same birthday as me wow❤
@ayomideunuis7721
@ayomideunuis7721 10 күн бұрын
How do we save images to the cloud? How is it saved?
@amogelangsekhu3906
@amogelangsekhu3906 15 күн бұрын
Tbh, I'm still confused.
@MusaKhan-pe3ud
@MusaKhan-pe3ud 15 күн бұрын
wow so amazing presentation i wa very confused before when , i did not watch this vedio , now i realy got everything from this vedio , you have made me well understood.thanks mam plzz keep it up You have provided us with an excellent platform from which we get more information than any other platform. thanks
@deepthid8436
@deepthid8436 18 күн бұрын
What is the role of heat inactivated serum . What happens we use without heat inactivation.?
@shivangiaggarwal4709
@shivangiaggarwal4709 21 күн бұрын
Amazing! Loved it!!!
@rusticrick999
@rusticrick999 22 күн бұрын
Always use filtered tips to avoid carrying over aerosols that can cross contaminate samples.
@cindyyin2504
@cindyyin2504 22 күн бұрын
Very good video
@ThomasPlatt1975
@ThomasPlatt1975 26 күн бұрын
That's awesome, but I am a food service director, what does this have to do with my life?
@syedahumairagillani9510
@syedahumairagillani9510 26 күн бұрын
Thank you for this video. Would you please elaborate how to design primers for SNP denotyping in qPCR? Which tool could beused and what are the steps? Thank you in advance.
@saisureshbandla3122
@saisureshbandla3122 26 күн бұрын
please explain about the relative quantification in detail with delta-delta ct method
@eloi2424
@eloi2424 Ай бұрын
Merci beaucoup pour ce vidéogramme. En effet, les explications sont à la fois riches et utiles. Un grand bravo. Au revoir. À bientôt. Bisous.
@sitarampadhy8716
@sitarampadhy8716 Ай бұрын
It's a innovative
@krishlabiaga
@krishlabiaga Ай бұрын
I hope to get accepted🤞
@ritishasingh9318
@ritishasingh9318 Ай бұрын
i have so many data to mine if anybody help me out how to mine data from gene mapper
@ritishasingh9318
@ritishasingh9318 Ай бұрын
i have to mine data from gene mapper i run multiple primer but now i done have any idea how to mine data from gene mapper can anybody help
@thermofisher
@thermofisher 29 күн бұрын
Hello Ritisha Singh, Thanks for your question. Can you please reach out to our technical support team at thermofisher.com/askaquestion. They would be the best team to assist. Thank you!
@borderlineRetardedSomoan
@borderlineRetardedSomoan Ай бұрын
greenspot,tennesee/vpn/root/youtube
@borderlineRetardedSomoan
@borderlineRetardedSomoan Ай бұрын
catman ai
@mosyoutubeanimals
@mosyoutubeanimals Ай бұрын
What happens if we wipe down the cathode side too?
@AWICKEDVIXEN1999
@AWICKEDVIXEN1999 Ай бұрын
If they delivered our own rna/dna I would ageee with this but sadly its gmo rna & dna
@tadamduluza2223
@tadamduluza2223 Ай бұрын
Very informative, nice video 😊
@nobody4191
@nobody4191 Ай бұрын
Does this mean it can be used de novo ?
@shreeshree5333
@shreeshree5333 Ай бұрын
Thank you for the useful video sir
@PALINDROMA.
@PALINDROMA. Ай бұрын
This is really good, thanks :)
@user-uk6ke9bx5d
@user-uk6ke9bx5d Ай бұрын
The reducing reagent is DTT, not LDS. LDS is in sample buffer,
@ldaimry
@ldaimry Ай бұрын
❤❤
@Elonmustard675
@Elonmustard675 Ай бұрын
I have no Affiliation with Gene Art services dashboard.
@pexotrexo3296
@pexotrexo3296 Ай бұрын
Finally Perfect explanation 🥲
@ashfaquekanhar9630
@ashfaquekanhar9630 Ай бұрын
thanks
@zeinebzeinouba8318
@zeinebzeinouba8318 Ай бұрын
Bonjour svp un vidéo de résolution des erreur possible sur pw 40 exemple erreur position 0.1 merci
@sheepmountaincabin3314
@sheepmountaincabin3314 Ай бұрын
2:26 "The y-intercept is the expected Ct value for a 1ng/uL sample". What?? That doesn't make any sense. The y-intercept represents the lowest quantity that can be detected, theoretically not zero, but essentially zero. Ideally, the Y-intercept is the number of cycles in your assay. The practical role of the y-intercept value is that it is used in a formula to take Ct's of unknowns and calculate starting quantities.
@lalitasharma6687
@lalitasharma6687 Ай бұрын
What are the instruments we use here can you please list them
@nadiarai7603
@nadiarai7603 Ай бұрын
Wow great video . Thank you so much. This is the video I was waiting for.
@user-zz7un9hb8l
@user-zz7un9hb8l 2 ай бұрын
Yay!!! 😭 amazing true super heroes! 🦸‍♀️
@Kitchesthetic__
@Kitchesthetic__ 2 ай бұрын
Anybody tell me how to make poster on it😭
@juliensiefridt4971
@juliensiefridt4971 2 ай бұрын
thank you so much, i've been struggling to understand this and you explained it perfectly 😩😩😩😩
@jonbaker5935
@jonbaker5935 2 ай бұрын
Wonderful company to work for.
@sofianbio4997
@sofianbio4997 2 ай бұрын
Can u please explain that on the device from zero to last step and give us a calculator example as a mathematical way thanks
@nileshadagale8874
@nileshadagale8874 2 ай бұрын
I use this instrument Count check same sample why variation cell count?
@rickh9908
@rickh9908 2 ай бұрын
❤️ Promo`SM