IHC Technical Resources

Protocols, optimization tips,
troubleshooting guides,
and more for IHC.

Troubleshooting guides

Troubleshooting guides

Download troubleshooting
handbooks for IHC, Western
blot and ELISA for FREE.

Tip: For comprehensive troubleshooting resources, download our troubleshooting guides.

For personalized troubleshooting assistance, contact us at support@bosterbio.com.

IHC Troubleshooting: High Background

You can typically expect some amount of background staining during IHC. However, once the level of background staining becomes high enough to obscure important features and structures of the tissue, steps must be taken to reduce it. Background staining can be caused by inappropriate antibody binding or by mistakes during the preparation of the tissue slide. Use this guide to resolve your high background staining:

Problem Cause Solution
Antibody binding incorrectly Excessive primary antibody concentration Titrate antibody to determine optimal concentration
Secondary antibody non-specific binding Run a negative control without primary antibody to assess secondary antibody binding
Use a secondary antibody pre-adsorbed against the immunoglobulin of the sample species
Block your sample with serum from same host as secondary antibody
Antibody cross-reactivity Use Boster primary antibodies guaranteed specific to only their listed targets
Improper preparation of tissue section Insufficient blocking Increase blocking incubation time
Use a different blocking reagent
Insufficient quenching of endogenous peroxidase or phosphatase Quench endogenous peroxidase with 3%H2O2 solution
Quench endogenous alkaline phosphatase with 2mM levamisole
Insufficient biotin or lectin blocking Block endogenous biotin with=streptavidin solution
Block endogenous lectins with alpha-methyl mannoside buffer
Incomplete deparaffinization Increase deparafinization time and use fresh dimethylbenzene
Tissue section too thick for complete reagent penetration Prepare thinner sections
Improper incubation parameters Incubation temperature too high Incubate at 4C
Too much substrate was used Reduce substrate concentration
Reduce substrate incubation time
Choose a substrate with higher signal:noise ratio (e.g. metal-enhnaced DAB)
high background staining of rat brain tissue stained with anti-VCP antibody

high background staining of rat brain tissue using anti-VCP antibody

improved staining of rat brain tissue using Boster troubleshooting tips

Improved staining of VCP in rat brain tissue