12 months from date of receipt, 2 to 8 °C as supplied
应用 | 稀释度 |
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IHC-P | N/A |
Anti-Rabbit and Mouse HRP-DAB IHC detection kit utilized the newest biotin-free polymerization technology to prepare super sensitive polymeric peroxidase linked conjugates. It utilizes a novel controlled and compact enzyme polymerization technology to achieve higher sensitivity without background. It provides on step detection protocol, superior sensitivity and specificity, short incubation time and faster turnaround.
Prior to staining the formalin-fixed paraffin tissue sections should be deparaffinized and hydrated following heat-induced epitope retrieval or enzyme pretreatment. Endogenous peroxidase should be blocked. Then add primary antibody and incubate at optimal titration and condition. After that add OneStep polymer HRP Goat anti-Rabbit and Mouse IgG (H+L) (specific for IHC) and incubate for 15-30 minutes. Polymer HRP will catalyze DAB to form visible brown deposit at the antigen site. When color development achieved satisfactory level, the slides are washed in water to stop reaction. The stained slides may be mounted with either aqueous mounting or organic mounting medium.
Immunohistochemistry protocol:
IHC shows positive staining in paraffin-embedded human stomach. Anti-Claudin18.2 antibody(S0B2069) was used at 1/1000 dilution, followed by anti-Rabbit and Mouse HRP-DAB IHC detection kit. Counterstained with hematoxylin.
Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human gastric cancer. Anti-Claudin18.2 antibody(S0B2069) was used at 1/1000 dilution, followed by anti-Rabbit and Mouse HRP-DAB IHC detection kit. Counterstained with hematoxylin.
Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.