protein complexes are immunoprecipitated without antibody contamination. Manufacturer: Thermo Scientific™ PI Catalog No. PI $ / Each. It is the Pierce kit.I have also read articles where the kit was used successfully, but it does not seem to work for me. I am loosing my. pierce pdf reader. Quote. Postby Just» Tue Aug 28, am. Looking for pierce pdf reader. Will be grateful for any help! Top.
|Published (Last):||3 May 2007|
|PDF File Size:||16.12 Mb|
|ePub File Size:||7.21 Mb|
|Price:||Free* [*Free Regsitration Required]|
Can someone who has had success performing Co-IPs help me troubleshoot problems I am experiencing.
I have been trying to carry out a Co-IP for several months now, but I believe that either my kit or my antibody is sub-optimal. Can someone suggest a good Co-IP kit to use which has proven successful for them?
If you really want a co-IP kit, there is a selection to choose from. I never brought a kit for co-IP.
If you have done IP before, co-Ip is just to “tune-down” your detergents in the lysis and wash buffers, otherwise the steps are the same. Thank you for your response. I have actually used one the Co-IP kits on the list you sent the link to, but I am having problems with it.
It is the Pierce kit. I have also read articles where the kit was used successfully, but it does not seem to work for me.
ANTIQUE OLD DR J TOWNSEND’S SARSAPARILLA NEW YORK GREEN GLASS BITTERS BOTTLE 10″ | eBay
I am loosing my protein before elution, which means that there is a problem with the antibody binding to the resin I think? I am following the protocol to the letter, but I am loosing my protein. I suspect it is the antibody. How do you ensure that the antibody you use will be piere for the reaction? Now, the real issue that you are encountering is- whether your antibody pierec suitable for IP?
Have you tried to address this issue before 21649 to the co-IP experiment? Yes, I have been doing the IP now with this antibody.
You are correct, I have a feeling it is the antibody as well, but I have already purchased a new antibody and made sure that it was purified and dissolved in PBS, not Tris.
pierce pdf reader – PDF Files
Those were the 2 main criteria for selecting an antibody. That is why I am not sure why it is still not working.
I do detect it, but in the 2nd wash which suggests that I have lost all my protein before elution. The buffers are all pre-optimized for this kit and should 261449 be too stringent for the reaction.
26149 pierce pdf editor
If it is the antibody, how do I go about ensuring that I have purchased the right antibody? I would appreciate any insight into this problem since I am able to figure out where the problem lies.
Log in or register to post comments. Hi Sue, If you piece want a co-IP kit, there is a selection to choose from. Yes, I have been doing the IP.