Citrate Buffer

ABIN1689349 产品详细信息, 供应商: Log in to see
Immunohistochemistry (IHC)
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Supplier Product No.
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产品特性 This product, after dilution, is to be used on formalin-fixed, paraffin-embedded tissue sections mounted on glass slides for target retrieval prior to immunohistochemical (IHC) procedures. When performed using this reagent and elevated temperature, target retrieval can disrupt the covalent bonds formed by formalin in tissue. Removal of these bonds can allow renaturation of protein molecules and increased antibody accessibility, which in turn can result in increased antibody binding (and thus increased staining intensity) and improved signal to noise rations. This type of result is observed with many primary antibodies.
实验流程 1. Deparaffinize and rehydrate tissue sections.
2. Dilute the product 1:100 with deionized water. Example: 2 ml of concentrate diluted in 198 ml of deionized water.
3. Immerse sections in coplin jar filled with diluted Citrate Buffer reagent..
4. Microwave on HIGH power until boiling.
5. Keep the slides warm by heating for 10 minutes on LOW power.
6. Let coplin jar sit in microwave for at least 20 minutes.
7. Remove and rinse with water.
8. Rinse with buffer and proceed with the appropriate staining protocol for the primary antibody in use.
限制 仅限研究用
状态 Liquid
浓度 100 X
缓冲液 Citrate, pH 6.0. 100X concentrate.
注意事项 1. Take reasonable precautions when handling reagents. Wear appropriate Personal Protective Equipment.
2. Avoid contact of reagents with eyes, mucous membranes and skin. If reagents come into contact with sensitive areas, wash with copious amounts of water.
3. Consult local or state authorities with regard to recommended method of disposal.
4. Avoid microbial contamination of reagents.
储存条件 RT
储存方法 Store at room temperature.. The user must validate any other storage conditions. When properly stored, the reagent is stable to the date indicated on the label. Do not use the reagent beyond the expiration date. There are no definitive signs to indicate instability of this product, therefore, positive and negative controls should be tested simultaneously with unknown specimens.