Mounting Medium With PI - Aqueous, Fluoroshield

Fluoroshield mounting medium with PI is an aqueous mounting medium for preserving fluorescence of tissue and cell smears. This unique formula prevents rapid photobleaching of FITC, Texas Red, AMCA, Cy2, Cy3, Cy5, Alexa fluoro 488, Alexa fluoro 594, Green fluorescent protein (GFP), tetramethyly rhodamine, Redox, Phycoerythrin (RP-E), Phyocyanin (PC), and Allophycocyanin (APC). The fluorescence is retained during prolonged storage at 4°C in the dark. This medium does not contain phenylenediamine, which destroys immunofluorescence of Cy dyes, RP-E, PC and APC. This mounting medium is fortified with PI which is a counter-stain for DNA. This product is to be used in in situ hybridization techniques or other methods where fluorescence of DNA staining is required. PI excites at 535nmn and emits at 615nm, producing a red fluorescence. RNA is also stained with PI.

Procedure

1. Bring the vial to room temperature.
2. Rinse slide to be mounted with distilled or deionized, touch the edges of slide on a paper towel to remove excess water. Place slides on a flat surface away from light.
3. Turn the vial upside down and remove any air bubbles.
4. Apply 3-4 drops directly of mounting medium on top of the specimen and spread out evenly by tilting the slide back and forth or spread evenly with a 0.2 ml plastic pipette tip, making sure the tissue is not touched. Excess medium can be removed by touching the edges of slide on paper towel.
5. Let stand at room temperature for about 5 minutes.
6. Apply cover slip, carefully avoiding air bubbles.
7. The specimen is ready for visualization under microscope.
8. One can seal the edges of cover slip with nail polish or any organic medium or Organo mounting medium (Limonene Mounting Medium ab104141). If coverslip is not sealed air bubbles will appear in few days.
9. For long term storage it is recommended that the slide be stored in the dark at 2-8°C.

Removal of Coverslip

Coverslip can be removed before sealing the edges. Soak slide in warm (37°C) water for a few minutes. Carefully and slowly move the coverslip. Soak in water an additional few minutes and remove coverslip. Rinse slide several times with warm water to remove all mounting medium. The slide can be remounted again.

Mounting Medium with PI (Propidium iodide) ab104129 (previously called Fluoroshield Mounting Medium with Propidium Iodide) is an aqueous anti-fade mounting medium designed to preserve fluorescence when imaging tissues and cell samples. It is fortified with propidium iodide as a counter-stain for DNA.

The formulation prevents rapid photobleaching of FITC, Texas Red, AMCA, Cy2, Cy3, Cy5, Alexa fluoro 488, Alexa fluoro 594, Green fluorescent protein (GFP), tetramethyly rhodamine, R-Phycoerythrin (R-PE), Phyocyanin (PC), and Allophycocyanin (APC).

Fluorescence is retained during prolonged storage at 4°C in the dark. This medium does not contain phenylenediamine, which destroys immunofluorescence of Cy dyes, R-PE, PC and APC.

Mounting media products

For fluorescent cell and tissue staining, Abcam recommends aqueous, anti-fade Fluorescence Mounting Medium Anti-Fade Fluorescence Mounting Medium - Aqueous, Fluoroshield ab104135, Mounting Medium with DAPI Mounting Medium With DAPI - Aqueous, Fluoroshield ab104139, and this product, Mounting Medium with PI ab104129. For thick sections or tissues containing lots of fat, we recommend Glycerol Mounting Medium with DAPI Glycerol Mounting Medium - Anti-Fade with DAPI ab188804.

For chromogenic immunohistochemistry, such as with DAB, AEC, or Fast Red, we recommend aqueous Mounting Medium Mounting Medium for IHC - Aqueous ab64230, or organic Limonene Mounting Medium Limonene Mounting Medium ab104141.

Procedure

• Bring the vial to room temperature.
• Rinse slide to be mounted with distilled or deionized, touch the edges of slide on a paper towel to remove excess water. Place slides on a flat surface away from light.
• Turn the vial upside down and remove any air bubbles.
• Apply 3-4 drops directly of mounting medium on top of the specimen and spread out evenly by tilting the slide back and forth or spread evenly with a 0.2 ml plastic pipette tip, making sure the tissue is not touched. Excess medium can be removed by touching the edges of slide on paper towel.
• Let stand at room temperature for about 5 minutes.
• Apply cover slip, carefully avoiding air bubbles.
• The specimen is ready for visualization under microscope.
• One can seal the edges of cover slip with nail polish or any organic medium or Organo mounting medium (Limonene Mounting Medium ab104141). If coverslip is not sealed air bubbles will appear in few days.
• For long term storage it is recommended that the slide be stored in the dark at 2-8°C. Removal of Coverslip Coverslip can be removed before sealing the edges. Soak slide in warm (37°C) water for a few minutes. Carefully and slowly move the coverslip. Soak in water an additional few minutes and remove coverslip. Rinse slide several times with warm water to remove all mounting medium. The slide can be remounted again.