Leica BIOSYSTEMS NCL-g-SARC Mode D'emploi page 6

Immunohistochemistry methodology for using Novocastra
frozen muscle tissue.
Reagents required but not supplied
1. Standard solvents used in immunohistochemistry.
2. 50 mM Tris-buffered saline (TBS) pH 7.6.
3. Antibody diluent - normal serum optimally diluted in TBS.
4. Normal serum from the species in which the secondary antibody is raised.
5. Secondary peroxidase-conjugated antibody - use as recommended by manufacturer.
6. 3,3' Diaminobenzidine tetrahydrochloride (DAB) - prepare and use as recommended by manufacturer.
7. Mounting medium - use as recommended by manufacturer.
Equipment required but not supplied
1. Incubator set to 25 C.
o
2. General immunohistochemistry laboratory equipment.
3. Electric fan for air drying slides.
Antigen retrieval solutions (see Recommendations on Use)
Not applicable to frozen sections.
Methodology
Prior to undertaking this methodology, users must be trained in immunohistochemical techniques.
Users should determine optimal dilutions for antibodies. Unless indicated, all steps are performed at 25
1. Cut and mount 4–10 µm sections on slides coated with a suitable tissue adhesive and air dry for at least one hour.
2. Incubate sections with optimally diluted primary antibody (see Recommendations on Use).
3. Wash in TBS buffer for 2 x 5 minutes with gentle rocking.
4. Incubate sections in appropriate peroxidase-conjugated secondary antibody.
5. Wash in TBS buffer for 2 x 5 minutes with gentle rocking.
6. Incubate the slides in DAB.
7. Rinse the slides in clean water.
8. Dehydrate, clear and mount sections.
Amendments to Previous Issue
.
Not applicable
Date of Issue
4 February 2008 (CEprotocol/Frozen Muscle).
G-SARC-CE
Page 5
antibodies on
TM
C.
o