And I belive when you referring a segment here ..it means you referring the a gene in side that chromosome....bcl6 gene you targeting by bcl6 probe against chromosome 8 to find a pattern fusion or red or green color to conclude normal or abnormal at loci 8q24 for example...
Thank you so much dear..can you please give a session on FISH ISCN nomenclature ..I am not able to get a clear picture on the notations from various cases
hi great video, but i have a question here that needs further clarification, this FISH method is done inside the nucleus of a cell of interest and is viewed under microscope, my question is how do the designed probe attaches itself to the un-denatured DNA strands that are present inside the cell nucleus or that this FISH method targets mRNAs instead?
Actually the probes designed are specific against the gene of interest. Your question is how does the hybridization occur with in the nucleus as the reaction is in-situ. Apparently, the DNA of interest is denatured leaving the strand of interest partially apart and the designed fluroscent probes are incorporated and raised which are complementary to the DNA of interest and the intensity of flourescence is measured
Your explanation is very clear sir..... best teacher
Thank you so much for appreciating my efforts
Thank you Mr. Suman,
your explanation is very clear.
King of biology 💫👍
Thank you so much for appreciating my efforts
Thank you so much sir
Apna Vedio gulo sob somoy e khub helpful hoi💖🙏
You're welcome. Glad to hear that you're getting benefit from my lectures
Very useful. Even I have future planing of doing FISH. I must say i have seen multiple videos this not at all fishy. Keep pouring your knowledge.
Thank u so much sir .... a big fan of ur vedioes and physical mapping in clear through this vedio
Thank you so much for appreciating my efforts
Thankyou so much sir,it helped me a lot
You're welcome
Thanks sir for making this video it's very helpful for me 😊
You're welcome
Thank you so much sir. This is very very helpful.
You're welcome
Thank you so much 😊 sir 🙏 for these videos..And for making Gene Mapping crystal clear 🙏😊.
You're welcome. Glad to hear that you're getting benefit from my lectures
A very nice video. Keep going and spread the knowledge 👍👍
You're welcome. Glad to hear that you're getting benefit from my lectures
And I belive when you referring a segment here ..it means you referring the a gene in side that chromosome....bcl6 gene you targeting by bcl6 probe against chromosome 8 to find a pattern fusion or red or green color to conclude normal or abnormal at loci 8q24 for example...
You are the saviour...🙏 thank you very much
It's very helpful. Thank you
You're welcome
Thank you so much dear..can you please give a session on FISH ISCN nomenclature ..I am not able to get a clear picture on the notations from various cases
Is the genetic material not lost when we are cutting the dna for insertion of neuclotides???
But Sir How we know that probe is bind with our gene in which chromosome number(1,2,3,....
I must admit, your looks deceived me into thinking it will be one of those garbage videos, but boy was I wrong. Very well explained.
That's pretty rude
What is denaturation temperature
hi great video, but i have a question here that needs further clarification,
this FISH method is done inside the nucleus of a cell of interest and is viewed under microscope, my question is how do the designed probe attaches itself to the un-denatured DNA strands that are present inside the cell nucleus or that this FISH method targets mRNAs instead?
Actually the probes designed are specific against the gene of interest. Your question is how does the hybridization occur with in the nucleus as the reaction is in-situ. Apparently, the DNA of interest is denatured leaving the strand of interest partially apart and the designed fluroscent probes are incorporated and raised which are complementary to the DNA of interest and the intensity of flourescence is measured
Ervin Chan which DNA is taken for making probe?
THANK U VERY MUCH SUMAN
happy b'day sir
Uddhav Kumawat thank u
Awesome sir
You're welcome
Thank u so much
You're welcome
I am confused you said dutp but RNA IS NOT deoxy only DNA IS DEOXY
Same doubt
Very helpful... Thanks..🙂
Thank u so much it's so great
What is genetic marker??
Specific genes
great video👏👏👏
At around 18:50 what do you mean by "plating chromosomes"??
+Farouk Aizat "painting chromosomes" ! it's like a comparative molecular cytogenetics technique
Thanks
thnks😊
It is now understood that I did not get that far
graziah