Комментарии:
Which topics should be next? Please make suggestions here:
ОтветитьSo helpful and clear, thanks!
Ответить👏👏
ОтветитьAfter denaturation, why will the target chromosome will hybridized with the probe instead of rebinding to its original strand?
ОтветитьCan FISH detect mosaicism in an adult?
ОтветитьGibt es auch ein Video auf deutsch ?
ОтветитьThat was very helpful, thank you <3
ОтветитьCell fixation
Adding probe
Denaturation
Hybridisations
Denaturation
ОтветитьAdd probe
ОтветитьFixation of cell et formaldehyde
ОтветитьFluorescent in situ hybridization
ОтветитьThis video was real good!
Ответитьthank you
ОтветитьEnglish is my second language and the way you talk very slow was just amazing for me, because I'm studying about FISH in my university in Brazil and I'm so proud of me to studying in English. By the way I have a test today wish me luck!
ОтветитьThanks, that was easy to follow and understand.
ОтветитьNever thought this is how fish are made.
ОтветитьHow the deletion site is known . And what confirms that probe is bound like how it gives signal after binding to dna
ОтветитьThis was soooo helpful,,thank you
ОтветитьThanks. Is it possible to tell which test do I have to do when I'm facing a syndrome?
ОтветитьThanks. I need to know how to figure out the used probes! For example: we have thousands of syndromes, do i have to make probes for all of them (especially if I have no idea about symptoms)?
Ответитьyou sound soo german :)
ОтветитьReally Thank u so much sir for this video ☺️ it helped me a lot to do my seminar ....God bless you 🙏
ОтветитьThank youu !!
Ответить👍
ОтветитьThis helped me so much thank you for explaining in such a calm voice and tempo
ОтветитьUseful sir 👏
Ответитьsprich doch deutsch henrik
ОтветитьI have a question regarding dna sequence using FISH. "Is it possible to identify a particular gene sequence (for example - Amel Y) using FISH if there is lot of depurination (loss of adenine , guanine) in interested gene sequence ?"
Ответитьsome time it gives false negative results because some time probe are not properly designed and sometime
there is change in annealing temperature ?
Am I right sir or any other reason of false negative result ?
I don't understand... You never explained about the fish. Clickbait
ОтветитьExtremely awesome and relevant to the preimplantational genetic testing environment. Well done, clearly explained!
ОтветитьCrazy German scientist over here.
Thanks tho, it was very helpful!
Thank you! Really helpful!
ОтветитьYou try to give the video more brightness it will be great if you do
ОтветитьGreatly well explained
ОтветитьThanks very much ❤
ОтветитьNice explanation, You made the concept easy and digestible, thanks
ОтветитьThis is great!
Ответитьthank you !!
Ответитьthank you very much for this video!!!!,I understand all
ОтветитьThanks!
ОтветитьTHANKS! NEEDED FOR A PAPER
ОтветитьAn exemple of how to design a probe for a specific gene will be nice
ОтветитьThis video was so helpful, thank you for your effort
ОтветитьSo FISH can help in karotyping too?
ОтветитьHelped a lot thank you so much☺️
ОтветитьWarm greetings. The short video is very helpful . But how to identify the specific complementary site in a chromosome . Or how do we know to prepare the complementary probe , on what idea this can be produced? If possible kindly send the answers. Thank you. Dr. Rise de leema .
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