Radioimmunoprecipitation assay buffer

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Radioimmunoprecipitation assay buffer (RIPA buffer) is a lysis buffer used to lyse cells and tissue for the radio immunoprecipitation assay (RIPA). [1] [2] This buffer is more denaturing than NP-40 or Triton X-100 because it contains the ionic detergents SDS and sodium deoxycholate as active constituents and is particularly useful for disruption of nuclear membranes in the preparation of nuclear extracts. The stronger detergents in RIPA buffer (such as SDS) cause greater protein denaturation and decrease protein-protein interactions.

Recipe

RIPA buffer recipes vary slightly between authors and may include:

The following ingredients are optional and included as needed:

References

  1. Alcaraz C, De Diego M, Pastor MJ, Escribano JM (July 1990). "Comparison of a radioimmunoprecipitation assay to immunoblotting and ELISA for detection of antibody to African swine fever virus". J. Vet. Diagn. Invest. 2 (3): 191–6. doi: 10.1177/104063879000200307 . PMID   2094444.
  2. Ngoka LC (October 2008). "Sample prep for proteomics of breast cancer: proteomics and gene ontology reveal dramatic differences in protein solubilization preferences of radioimmunoprecipitation assay and urea lysis buffers". Proteome Sci. 6 (1): 30. doi: 10.1186/1477-5956-6-30 . PMC   2600628 . PMID   18950484.