Luminescent Conjugated Oligothiophenes (LCO) Staining

Hemanth Ramesh Nelvagal, Toby J Curless, Zane Jaunmuktane

Published: 2023-12-08 DOI: 10.17504/protocols.io.x54v9pd7pg3e/v1

Abstract

The protocol describes Luminescent Conjugated Oligothiophenes staining on brain sections.

Steps

Preparation

1.

Generate tissue sections using standard microtome sectioning protocols.

2.

Heat tissue dry tissue sections for 1h 0m 0s at 60°C

Deparaffinisation and LCO Staining

3.

Safety information
Please refer to the Xylene Data Safety Sheet and follow local approved risk assessements and protocols for safe handling and disposal of xylene.

De-paraffinise sections by 0h 5m 0s washes in xylene (x2), 0h 5m 0s 100 % ethanol (x2) and 0h 5m 0s in DEPC H2O (x1).

4.

Circle tissue on slide using a hydrophobic ImmEdgeTM PAP pen (Vector laboratories) to contain

solution.

5.

Prepare 1:500 pFTAA solution (diluted in PBS). All steps from here should be performed away from light.

6.

Pipette pFTAA solution onto tissue and incubate at room temperature in a humidified chamber for 0h 30m 0smins.

7.

Wash slides in PBS 3x.

8.

Coverslip slides using HydromountTM aqueous non-fluorescing mounting media (National Diagnostics).

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