Immunohistochemistry against p62 and LBP110

Dennis de Bakker

Published: 2024-07-31 DOI: 10.17504/protocols.io.kqdg32b47v25/v1

Abstract

Immunohistochemistry staining co-labeling LBP110 and p62/SQSTM1 and DAPI.

Steps

Tissue preparation

1.

Day 1: Whole mouse brain (2 years old, male) was fixed overnight in 4%PFA.

2.

Day 2: Brain was washed 3x 5' in PBS + 4% Sucrose

3.

Day2: Brain was incubated overnight in PBS + 30% Sucrose

4.

Day3: Brain was embedded into optimal cutting medium (OCT)

5.

Day3: Brain was cut with a cryostat in 10um thick sections and stored at -80C

Antibody staining protocol day 1

6.

Slides with brain tissue sections were thawed 0h 15m 0s Room temperature

7.

Add slides to glass coplin Jar.

8.

Wash 3x 0h 10m 0s in PEMTx

9.

Move slides to plastic coplin jar for antigen retrieval

10.

Perform antigen retrieval 0h 15m 0s 85°C

11.

Let plastic coplin jar cool down to room temperature 0h 20m 0s

12.

Place slides back in original glass complin jar

13.

Wash 2x 0h 10m 0s in PEMTx

14.

Place slides horizontally in box humidified with MQ. Use hydrophobic pen to outline tissue sections.

15.

Add blocking buffer to the slides and incubate 1h 0m 0s

16.

Add antibody solution (blocking buffer + 1:100 LBP110 + 1:100 p62) and incubate 4°C

Antibody staining protocol day 2

17.

Wash slides 4x 0h 15m 0s

18.

Incubate with secondary antibody solution in humidified box (PEMTx + 2% BSA + 1:500 secondary antibodies + 1:1000 DAPI) for 1h 0m 0s

19.

Place slides back in coplin jar (keep in dark)

20.

Wash 3x 0h 10m 0s in PEMTx

21.

Wash 2x 0h 7m 0s in PEM

22.

Mount slides using Prolong Gold mounting medium and store at 4°C

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