Modified avidin-biotin technique

• US 5,281,521 A
• Filed: 07/20/1992
• Issued: 01/25/1994
• Est. Priority Date: 07/20/1992
• Status: Expired due to Term

• Current Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Original Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Inventors: Lee, Virginia M-Y., Trojanowski, John Q.
• Primary Examiner(s): SAUNDERS, DAVID A
• Application Number:
  US07/915,919
• Time in Patent Office: 554 Days
• Field of Search: 435/7.5, 435/962, 435/960, 435/7.92, 435/7.2, 436/548, 436/501, 530/388.1
• US Class Current: 435/7.5
• CPC Class Codes: G01N 2474/20 Immunohistochemistry assay
• CPC Class Codes: G01N 33/531 Production of immunochemical test materials
• CPC Class Codes: G01N 33/535 with enzyme label or co-enzymes, co-factors, enzyme inhibitors or enzyme substrates
• CPC Class Codes: Y10S 435/962 Prevention or removal of interfering materials or reactants or other treatment to enhance results, e.g. determining or preventing nonspecific binding

Abstract

A method for preparing an antigen specific probe is provided by incubating a primary antigen specific monoclonal antibody with a biotinylated secondary antibody to produce a complex of the primary and secondary antibodies. The staining pattern produced by these probes reflects the specificity of the monoclonal antibody in the complex and the labeling of irrelevant, endogenous immunoglobulins is reduced substantially. This novel, indirect immunohistochemical method can be used to study normal and diseased tissues using a variety of monoclonal antibodies.

Claims

1. A method for preparing an antigen specific complex comprising incubating a selected primary antigen specific monoclonal antibody which is not bound to said primary antigen with a selected biotinylated secondary antibody to produce a complex of the primary and secondary antibodies.

2. The method of claim 1 wherein said incubating step comprises incubating a selected volume of the primary antibody with an equal volume of the secondary antibody and subsequently adding diluted normal mouse serum to achieve a final concentration of about 1:

1200 to about 1;

3200.

3. The method of claim 2 wherein the incubating step is performed at a temperature of from about 35°

C. to about 39°

C. for up to 60 minutes.

4. The method of claim 2 wherein the incubating step is performed at 37°

C. for one hour.

5. The method of claim 2 wherein the selected volume is from about 0.5 ml to about 3.0 ml.

6. The method of claim 2 wherein the diluent for the primary antibody-biotinylated secondary antibody complex is 1% fetal calf serum in 0.1M TRIS buffer at pH 7.6.

7. The method of claim 2 further comprising chilling the complex of the primary and secondary antibodies at about 2°

C. to about 6°

C. for at least 30 minutes before it is applied to tissue sections.

8. The method of claim 1 wherein the selected secondary antibody is selected from the group consisting of biotinylated anti-mouse, biotinylated anti-rat or biotinylated anti-rabbit antibodies.