You said that you cleave the larger DNA fragments into smaller gene fragments... but if the functions are not known, how do you known when you're cutting a gene itself out and not halfway though a gene? Do you look for start/ stop codons first or something? And how do you separate the genes into different beakers, is it based on differential centrifugation...? I'm a little confused!
yes im confused as well. im assuming you can take the dna that has been run through the gel and then clone it and put them in beaker? i might be wrong, ive never run the gel electrophoresis before
you have to carry out partial dna digestion to improve your chances of having atleast one intact copy of each gene because indeed restriction enzymes don't respect gene boundaries. Later on you can look if the gene of interest is present by using a complementary strand.
Isn't it an audacious claim to make when you say that the restriction sites are present exactly at the intersection of 2 genes? I believe the restriction site locations will be extremely impossible to predict, as we never know where a palindromic sequence is supposed to be.
As far as I know, scientists use many different restriction enzymes on different copies of one genome to be sure to have the maximum representation (and to include the sequence they're seeking)
Does the restriction enzyme cut precisely one gene at a time or does the fragment sometimes include more (or less) than one gene? How does the restriction recognize where to cut?
can you tell me how the probe is going to get hybridised with the dna of interest?and how we are going to seperate that hybridised dna for further process?
Do we still (now) need a phage vector to replicate the gene fragments? Why can't we do a PCR to amplify the gene fragments in large number followed by insertion into e.coli and screen for our gene of interest?
How many recombinants has to be screened with 90 percent probbality of getting a gene if the size of genome is 8000kb and library was constructed in puc vector Please answer
I appreciate the amount of effort you put into your lectures and illustrations.
Oh my god thank you so much! I finally understand the entire process because of this video!
Ur videos help me in my genomics exam.. Thanks aloooooot ⭐️⭐️⭐️⭐️⭐️
Fantastic video this greatly helped me understand this topic
You said that you cleave the larger DNA fragments into smaller gene fragments... but if the functions are not known, how do you known when you're cutting a gene itself out and not halfway though a gene? Do you look for start/ stop codons first or something? And how do you separate the genes into different beakers, is it based on differential centrifugation...? I'm a little confused!
yes im confused as well. im assuming you can take the dna that has been run through the gel and then clone it and put them in beaker? i might be wrong, ive never run the gel electrophoresis before
you have to carry out partial dna digestion to improve your chances of having atleast one intact copy of each gene because indeed restriction enzymes don't respect gene boundaries. Later on you can look if the gene of interest is present by using a complementary strand.
your video has helped me alot🌟🌟🌟🌟🌟
you are so clear! i love your videos
please make more
Thank you. Your videos are super helpful.
Isn't it an audacious claim to make when you say that the restriction sites are present exactly at the intersection of 2 genes? I believe the restriction site locations will be extremely impossible to predict, as we never know where a palindromic sequence is supposed to be.
As far as I know, scientists use many different restriction enzymes on different copies of one genome to be sure to have the maximum representation (and to include the sequence they're seeking)
Explained so well!
thank you sir......it's very heipful for me...…..thanks again
Does the restriction enzyme cut precisely one gene at a time or does the fragment sometimes include more (or less) than one gene? How does the restriction recognize where to cut?
Thank you so much :) this was very helpful
your videos are awesome. thank you.
this was awesome, thank you!!!
many thanks! I fink it very useful and easy to comprehend
THANKS A BUNCH !
wow u r very good!
You're the coolest *_* thanks a bunch
can you tell me how the probe is going to get hybridised with the dna of interest?and how we are going to seperate that hybridised dna for further process?
Do we still (now) need a phage vector to replicate the gene fragments? Why can't we do a PCR to amplify the gene fragments in large number followed by insertion into e.coli and screen for our gene of interest?
Thank you very much
Where is the “plasmid” version specifically please
How many recombinants has to be screened with 90 percent probbality of getting a gene if the size of genome is 8000kb and library was constructed in puc vector
Please answer
0.15
Use Clark and Carbon formula
N=ln(1-95%)/ln(1-1/3)
great!
Is this shotgun cloning?
did he skip #4?? orrr?
Thanks....my name also.Ak 😉
Tq so much
thank you sir
thanks
R u a physician???
inspiration
He coughs at 4:40
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