INSTRUCTIONS FOR IMMUNOHISTOCHEMICAL STAINING INTRODUCTION Medico adopts a new polymerase-mark system (poly- HRP conjugate Goat Anti-mouse IgG). More enzymes will connect to the single antibody through the arm structure. Meanwhile, the optimal structure of new system enhences the signal during immunochemistry and reduce the experimental steps. Reagents supplied
component size storage Blocking Serum 20ml Store at 4°C for 1year poly- HRP-Goat Anti-Mouse IgG 15ml Store at 4°C for 1year Reagent A 20×concentrated solution 1ml -20℃ Reagent B 20×concentrated solution 1ml 4-8℃ DAB substrate 20ml 4-8℃
- NOTE: Reagents not supplied (Primary Antibody, Antibody diluent buffer,) Reagent A (DAB) is a suspected carcinogen. Reagent B contains hydrogen peroxide, Handle with care.
PREPARATION OF FineTest WORKING SOLUTIONS
- A number of different buffers can be used in the IHC system. One of the most common is 10 mM sodium phosphate, pH 7.4, 0.9% saIine (PBS). PBS-T (PBS+0.1% Tween 20)
- Primary Antibody working solution: according to the dilution ratio provided by the manufacturer.
- Blocking Serum and poly- HRP Goat Anti-Mouse Ig G: ready-to-use
- DAB working solution (1ml): Mix 50ul of Reagent A , 50ul Reagent B and 900ul DAB substrate in a EP tube. For using, it is best to use DAB working solution within 20 minutes
- The configuration table
Blocking Serum Working solution poly-HRP-Goat Anti-mouse IgG DAB Working solution 1 section 50ul-100ul 70ul 100ul 10 sections 0.5ml-1ml 0.7ml 1ml 100 sections 5ml-10ml 7ml 10ml 200 sections 10ml-20ml 14ml 20ml STAINING PROCEDURE FOR PARAFFIN SECTIONS
Deparaffinize and hydrate tissue sections through xylenes or other clearing agents and graded alcohol series.
Rinse for 5 minutes in tap water.
If quenching of endogenous peroxidase activity is required, incubate the sections for 30 minutes in 0.3% H2O2 in methanol or water. Incubation times may be shortened by using higher concentrations of H2O2. If endogenous peroxidase activity does not present a problem, step 3 may be deleted.
Wash in buffer for 5 minutes.
Incubate sections for 1 hour at 37℃ with Blocking Serum
Blot excess Blocking Serum from sections.
Incubate sections for 1 hour at 37℃ or Overnight at 4℃ with primary antibody diluted in PBS buffer. (If background staining occurs, dilutions of the primary antibody may be made in buffer containing 0.1% of BSA, See Note 3, 5)
Wash slides for 3 minutes in PBST buffer.
Incubate sections for 1 hour at 37℃ with poly- HRP Goat Anti-Mouse Ig G.
Wash slides for 3 minutes in PBST buffer.
Incubate sections in DAB working solution until desired stain intensity develops. (See Note 2)
Rinse sections in tap water. 15. Counterstain, clear and mount.
Solutions containing sodium azide or other inhibitors of peroxidase activity should not be used
Development times may differ depending upon the level of antigen, the intensity of the stain that is required, or the substrate used. DAB generally should be developed for 2-10 minutes; AEC for 10-30 minutes; TMB for 5-20 minutes. Some counterstains may not be compatible with certain peroxidase substrates because of solubility of the reaction products or lack of color contrast. A counterstain compatibility chart is available upon request.
Only immunohistochemical grade BSA should be used, as other preparations can containundesired impurities. Dilution of these reagents may require longer incubation times and/or higher incubation temperatures to achieve maximum sensitivities.
The section should be well prepared. Fixation (generally, in buffered formalin not exceeding 4 percent formaldehyde) should be sufficient to maintain the integrity of the section throughout the staining procedure but not so harsh as to destroy the antigen under study. During the staining procedure, do not allow the section to dry out. Use a humidified chamber for incubations.
To avoid adsorption of the antibody to the plastic or glass container in which the final dilution is made, the primary antibody may be diluted in buffers containing 0.1% immunohistochemical grade bovine serum albumin.
Incubation times may be shortened. In cases where the antigen concentration in the section is high, suggested incubation times with primary antibody, secondary antibody, and DAB Reagent may be reduced. If the antigen concentration is low, steps 7 and 9 may be lengthened to achieve maximal staining