10X EDTA buffer pH 8.0

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Product Details

Summary
Applications IHC, IHC-P

Order Details

10X EDTA buffer pH 8.0 Summary

Specificity
10x EDTA Buffer pH 8.0 for Heat Induced Epitote Recovery

Applications/Dilutions

Dilutions
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin
Application Notes
The antigen retrieval protocol is recommended for use in tissues that have been fixed in formalin only. Ensure that the fixed sections are adequately embedded in paraffin. Cut tissue sections to 4-5 microns.

Preparation of Working Solutions
1. The 10X concentrated format should be diluted tenfold with distilled or deionized water.
2. Mix one part of concentrated Antigen Retrieval Solution with nineparts of deionized or distilled water.
3. Shake the bottle vigorously to completely mix the components of theconcentrate (the solution may separate into phases over time).
4. Store with cap tightly secured.

Protocol Recommendations
1. Deparaffinize and rehydrate tissue sections.
2. Place slides into 1X retrieval solution in a slide container (e.g. Coplinjar, Tissue-Tek, staining dish or metal slide canister).
3. Retrieve sections under pressure
4. After take-off reagent jar containing slides from pressure cooker, allow the slides to cool for 20 minutes to reach room temperature.
5. Wash slides in deionized water and then with wash buffer. Proceed with immunostaining recommendations in the antibody datasheet.
6. Gently rinse by gradually adding DI water to the solution, thenremove slides and rinse with DI water.

Packaging, Storage & Formulations

Storage
Store at room temperature.
Buffer
Dilute one part buffer with nine parts de-ionized or distilled water.
Preservative
No Preservative

Background

In order to perform immunostaining, the tissue specimens should be fixed in appropriate fixative. The purpose of such fixative is to conserve the tissue from autolysis, to preserve tissue structures and to immobilize antigens. However, this requires harsh treatment of the antigens. As a result, antigens undergo chemical alteration of their primary, secondary and tertiary structures. Because of changes in the protein containing epitopes or in neighboring proteins, antigenic sites may be masked. In past, enzymatic treatment with proteolytic enzymes i.e. pepsin, trypsin or pronase has been performed to regain the masked antigens. Shi et al. (1991) have reported that the treatment of the tissue section with heavy metal solution in a microwave can regain the masked antigens significantly. However, heavy metals in the solution increase the risk of exposure of lab personnel to lead. To solve this problem, we have developed a new antigen unmasking solution which is free from heavy metals. Use of this antigen unmasker can prevent the risk of unnecessary exposure to the lab personnel and also resolve the handling and disposal problems.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Support products are guaranteed for 6 months from date of receipt.

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