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Immunoprecipitation (IP) is the small-scale affinity purification of antigens using a specific antibody that is immobilized to a solid support such as magnetic particles or agarose resin.
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NP-40 Cell Lysis Buffer: Cell Lysis Buffer: M-PER Mammalian...
- Chromatin IP
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- GST-tagged Proteins
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- Co-IP
Whereas a number of antibody validation strategies can be...
- Biotinylation
Biotinylation, also called biotin labeling, is most commonly...
- Overview of Affinity Purification
Instead, epitope tags are more often used for small-scale...
- His-tagged Proteins
Affinity purification of His-tagged proteins. Cell lysate...
- Pull-Down Assays
The pull-down assay is an in vitro method used to determine...
- Cell Lysis Solutions
Immunoprecipitation (IP) is the technique of precipitating a protein antigen out of solution using an antibody that specifically binds to that particular protein. This process can be used to isolate and concentrate a particular protein from a sample containing many thousands of different proteins.
Immunoprecipitation (IP) is a method to isolate a specific antigen from a mixture, using the antigen-antibody interaction. Antigens isolated by IP are analyzed by SDS-PAGE or Western blotting.
9 sie 2016 · By using immunoprecipitation in combination with mass spectrometry (IP-MS) it is possible to verify that an antibody interacts specifically with an intended target.
Immunoprecipitation (IP) is defined as the isolation of an antigen using a specific antibody coupled (covalently or noncovalently) to a sedimentable matrix. From: Methods in Cell Biology, 2012
Immunoprecipitation (IP) is used to separate proteins that are bound to a specific antibody from the rest of a sample, while co-IP is used to identify protein–protein interactions between the protein that bound to the antibody used for IP and additional proteins that are detected by immunoblotting.
Individual Protein Immunoprecipitation (IP): Individual Protein IP utilizes an antibody to isolate a specific protein of interest from cell lysate. The antibody binds to the protein and subsequently, the antibody-antigen complex is extracted using protein A-G-coupled agarose or magnetic beads.