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Immunoprecipitation (No Protein Detected) severe

No Protein Detected: Lysis Buffer Incompatibility

Symptom
Target protein not detected in IP despite using sufficient antibody and confirmed protein expression. Antibody may fail to recognize target due to protein denaturation or improper folding.
Common Causes
  1. 1 Denaturing lysis buffer used with antibody that only recognizes native protein epitopes
  2. 2 Non-denaturing lysis buffer used when antibody requires denatured protein for recognition
  3. 3 Lysis buffer contains detergents or agents that disrupt antibody-antigen binding
  4. 4 Inappropriate buffer composition causes protein aggregation or precipitation
Solutions
  1. 1 Check antibody datasheet for recommended applications: IP typically requires antibodies that recognize native proteins
  2. 2 Use non-denaturing lysis buffer (e.g., 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% Triton X-100, protease inhibitors) for native IP
  3. 3 Avoid strong ionic detergents (SDS >0.1%, sarkosyl) or high urea concentrations that denature proteins
  4. 4 Verify lysis buffer compatibility with antibody isotype and adjust detergent type/concentration accordingly
Related Video (2)
Cell Signaling Technology ★ 78
Western Blotting Protocol
"Western blotting protocol demonstrates protein detection and handling, providing context for understanding antibody-protein interactions and proper sample preparation techniques"
Cell Signaling Technology ★ 72
How CUT&RUN Profiles Chromatin | Cell Signaling Technology
"CUT&RUN is presented as a low-cell-number alternative to chromatin immunoprecipitation, directly addressing IP methodology and antibody-epitope recognition challenges"
Source: abcam.com ↗
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