Co Immunoprecipitation | Immmunorecipitation | Co IP Assay Principle | Procedure | Technique |
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- เผยแพร่เมื่อ 21 ม.ค. 2025
- This video lecture describes
1. What is Immunoprecipitation (IP) ? How immunoprecipitation is used for the detection of protein of interest?
2. What is Co immunoprecipitation (Co-immunoprecipitation) (CO-IP)?
3. What is the principle and procedure of immunoprecipitation and co-immunoprecipitation ?
4. How Co immunoprecipitation (Co IP assay) can be used to study protein protein interaction ?
5. What is the difference between immunoprecipitation and co immunoprecipitation ?
6. Co immunoprecipitation steps
7. immunoprecipitation steps
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As a freshman who just start to read reseach articles, I have to look up and self-study a lot of concepts and methods of technologies that I was rarely taught at lower education level
So I really appreciate videos like this
Thank you!
You are most welcome. We are so happy that out videos are useful to the people like you. We wish you all the best with your studies 🤗
When we use magnetic beads, we don't need to spin the mixture. We use a magnet to pull them to the side of the tube. We spin when we use agarose beads.
Thanks for your insights 😊
Well done 👍
Thank you 😊
Great explanation thanks
You're welcome!
Excellent explanation sir ❤
Keep watching
Excellent 👌
Thank you! Cheers!
Excellent explanation 🙂
Thank you so much.
So what is the difference between both techniques? It seems as the same procedure, how do you make sure youre keeping the protein-complexes toghether?
Immunoprecipitation is used to isolate just one protein. We have an antibody for protein X. Protein X will attach to our antibodies which are attached to a bead. We can then pull these down with centrifugation and isolate protein X. Co-immunoprecipitation is used to determine protein protein interaction.s We would have a bead with an antibody for protein A. Once protein A is on our bead, we would then expose it to a solution of proteins. If our hypothesis is that protein A binds protein B, we will put protein B in the solution with the beads which have protein A attached. Then we will pull down these beads and run a something like a western blot to determine if protein B is present. If it is present, we know that it would only be present because of its attachment to protein A.
thank you
You are most welcome 🤗
What is the difference between immunoprecipitation & ELISA?