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Blocking of Unwanted Non-specific Staining for Immunohistochemistry
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Blocking of Unwanted Non-specific Staining for Immunohistochemistry

Dr. Giorgio Gattoretti

Associate Professor of Clinical Pathology
Institute for Cancer Genetics, Columbia University
New York, USA

Source of unwanted staining, besides poor knowledge of the antibody reactivity and malice, is due to:

Endogenous enzymes or fluorochromes.

Endogenous biotin.

Endogenous antibody binding activity (Fc receptors).

Cross reactivity of the secondary reagents with endogenous proteins.

Blocking of endogenous enzymes

Endogenous enzymes such as AlkPhos, AcPhos and esterases are destroyed by boiling even a short time at 100 ºC. Peroxidase is not.

Blocking of endogenous peroxidase is done by preincubating the slides in

3% H2O2
1% Sodium Azide
30 minutes
several washes

This mixture is more effective than 1.5% H2O2 in absolute methanol. Methanol incubation is also a fixation step that may affect your staining.

Blocking of endogenous Alkaline Phosphatase is done by exploiting the differential sensitivity of calf intestinal AP, used as a reporter, and leukocyte AP. This latter is inhibited, while the former is not by Levamisole 1 mM, which should be present in the development buffer.

Blocking of endogenous fluorochromes.

Blocking of endogenous fluorochromes is impossible. One may choose fluorochromes emitting in the UV range of spectrum, where endogenous autofluorescence of tissue is minimal.

Blocking endogenous biotin

Can be done with commercially available kits or by buying the isolated components of the kits, free biotin and free avidin.

Can also be done with simpler reagents as below.

1.  Wash twice in TBS 0.05M pH7.5, to which 0.01% Tween 20 has been added (TBS-T).

2.  Briefly blot the slides without letting them dry and then apply egg white in PBS-BSA-NaN3 as a blocking agent (one egg white in 100 ml PBS + NaN3) (Miller RT et al, Appl Immunohistochemistry 5(1): 63-66, 1997). Incubate for 10 min. minimum.

NOTE: this passage may be omitted, however subsequent double staining with a biotin based method may need endogenous biotin blocking.

3.  Wash once in TBS-T.

4.  Incubate with skim milk 5% in TBS-T for 10-30 min. (Miller RT et al, Appl. Immunohist & Molecular Morphology, 71(1): 63-65, 1999)

NOTE: skim milk may contain weak proteases which will be useful to further unmask antigens, but may reduce immunostaining by acting on primary Abs.

5- Wash once in TBS-T (residual milk can contribute to blocking).

Blocking of endogenous Fc blocking.

Specimens not paraffin embedded may have significant Fc binding activity by macrophages, B cells, T cells and other cell types.

By exploiting the preferential avidity of Fc receptor for human > mouse Ig> rabbit > swine > goat immunoglubulins, one may use a blocking of the receptors with a reagent which will not interfere with the secondary reagents and with which the secondary antibodies can be absorbed (1% serum added).

Blocking of cross reactive antigens in the tissue.

Typical example is staining mouse monoclonals in mouse tissue, where endogenous immunoglobulins will be specifically detected by the antibody aimed at the exogenous antibody used.

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