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Epredia™ Lab Vision™ EDTA Buffer for Heat-Induced Epitope Retrieval (10X)
Improve the reactivity of many antibodies in formalin-fixed tissues with Epredia™ Lab Vision™ EDTA Buffer for Heat-Induced Epitope Retrieval (10X).
1365.00 DKK
Specifications
| Content And Storage | Room temperature |
|---|---|
| Dilution | 10X |
| Product Type | EDTA |
| For Use With (Application) | Immunohistochemistry |
| pH | 8 |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
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12668286
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Epredia™
AP-9004-500 |
500mL | N/A | ||||||
Description
- 10mM EDTA buffer, pH 8.0
- Dilute 10-fold with distilled water before use
Storage Conditions: Store at room temperature. Stable for up to 18 months. Contains no preservatives. For periods longer than 3 months, store at 2-8°CProcedure:
1. Place five-micron thick tissue sections on glass slides coated with poly L-lysine or APTES.
2. Deparaffinize and rehydrate sections as usual.
3. Place slides in a Coplin jar containing 1mM EDTA buffer, pH 8.0; cover with a vented plastic wrap and place the jar in a steamer (Black & Decker™) for 20 minutes.
4. Take out the jar and let the sections cool in the jar for 20 minutes at room temperature. THIS STEP IS VERY CRITICAL AND SHOULD NOT BE AVOIDED.
5. Wash sections in buffer for 2 x 5 minutes.
6. Block endogenous peroxidase as usual.
7. Wash sections in buffer for 2 x 5 minutes.
8. Block nonspecific sites with normal serum as usual.
9. Place optimally diluted primary antibody on the sections (incubation time and temperature for a given set of experimental conditions should be determined by the investigator).
10. Wash sections in buffer for 2 x 5 minutes.
11. Remaining procedure is same as routinely performed in your laboratory.
Specifications
| Room temperature | |
| EDTA | |
| 8 |
| 10X | |
| Immunohistochemistry |
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