I've used this kit for DNA extraction from fresh blood sample but don't get any DNA at all. 4 times we failed using this kit. Then finally we changed this kit and shifted to another brand.
Your video is very didactic, congratulations for the effort and performance, your video helped me to establish the extraction protocol for my study. I would like to know where you got this methodology from so that I can quote it in my article, thank you in advance!
Hello, here I am again. In my synchronization, I can't get only adult individuals. Young individuals always appear as well. Does this also happen to you? Is there any way to remove fragments of worms after shaking with the bleaching solution?
Hi Gustavo, I have used a cell filter (blue) to remove the bodies that are left over after synchronization. Thus, the eggs will be in the filtrated solution.
Hello, how are you? Great video on chemotaxis with C. elegans! I would like to know if you have (or where you got it from) the complete protocol, as I would love to use it.
Hi Kenshiro, Happy to share here's the protocol we use for this lab: docs.google.com/document/d/1axDuy41I3ZZdNVmM55q_DOoF6Yq7qquGZsq8u1f0j5s/edit?usp=sharing
Amazing video, super useful and straight forward unlike some of the other tutorials online this one actually answered my question quickly and efficiently.
Thank you!
I've used this kit for DNA extraction from fresh blood sample but don't get any DNA at all. 4 times we failed using this kit. Then finally we changed this kit and shifted to another brand.
Thank you so much god bless you😊
benchling is free for academic account ?
Very nice, to change one letter you need entire software tutorial and 30 min archiving procedure. Very efficient.
Thank you! What does the bold red letters mean?
Your video is very didactic, congratulations for the effort and performance, your video helped me to establish the extraction protocol for my study. I would like to know where you got this methodology from so that I can quote it in my article, thank you in advance!
wow
Please help where are the results of your DNA isolation after AGE? As I'm unable to find, TIA
Thank you so much!! I think this is the only tutorial video on Foldit StandAlone in youtube
Very educational. Thank you for your great effort. I would like to know at what temperature did you incubate the sample in 50uL Elution Buffer?
Room temperature
What kits are your using?
why is it incubated at 56 degrees celcius?
Do you know where I can download the bagel b sequence? Or any sequence really
same
i usally go to NCBI > nucleotides > name of gene, to search for it
fortnite
nice
nice
Hello, here I am again. In my synchronization, I can't get only adult individuals. Young individuals always appear as well. Does this also happen to you? Is there any way to remove fragments of worms after shaking with the bleaching solution?
No need to care about that. After bleaching, only eggs left are live.
Hi Gustavo, I have used a cell filter (blue) to remove the bodies that are left over after synchronization. Thus, the eggs will be in the filtrated solution.
@@francinecoa3553 can you provide a catalog number for the cell filter?
Hello, how are you? Great video on chemotaxis with C. elegans! I would like to know if you have (or where you got it from) the complete protocol, as I would love to use it.
Hi Kenshiro, Happy to share here's the protocol we use for this lab: docs.google.com/document/d/1axDuy41I3ZZdNVmM55q_DOoF6Yq7qquGZsq8u1f0j5s/edit?usp=sharing
@@sbbiovideos Thank you so much !!! <3
46 THOUSAND VIEWS????? WOW!!!!!
How does this have no views! Explained it to me So well thank you.
thank you very much. it's really helpful!
Thanx a lot
Amazing video, super useful and straight forward unlike some of the other tutorials online this one actually answered my question quickly and efficiently.
thanks!! great video
Thank you this was really helpful!
The closed captions on this video is on a new level of goofy.
Brilliant Video, helped me alot, thankyou!
pretty helpful, thank you
a very good video. it clarified some things. I especially benefitted from your discussion of early embryonic development.
Really helpful! Thank you.
This was perfect, - Thank you!
thanx!!
great teaching! loved the lesson :)
you just saved my life!!!! thank you so much!!!!
thnx.......
Thank You!!!
This is a very informative video, thank you.
where is your lecture on the general mechanisms of transcriptional regulation?
dat video... thanks a ton madam
This is correct. Allolactose is the inducer which binds to Lac-I. Lac I is bound to the repressor and is turned off most of the time (inducible)
Whoever doesn't like this video is a hater. Thank you for the wonderful lecture!
Thank YOU, this was very helpful =)
THANK YOU SO MUCH. YOU MADE IT EASY TO ME.
you're a savior!
Lactose doesn't bind to the repressor. Allolactose, an isomer of lactose and a chemical signal binds to the repressor making it inactive. Right?
Great Video!!
Spot on thank you very much. Exactly what I was looking for.
Ok got it Chokrane ;D
This really helped with a uni assignment I had to do, thankyou!!!
Alternative splicing is it for transciptional or translational regulation or the two ? im confused..
Thanks a lot! Really cleared up some issues with me.