Immunohistochemistry against p62 and LBP110
Dennis de Bakker
Abstract
Immunohistochemistry staining co-labeling LBP110 and p62/SQSTM1 and DAPI.
Steps
Tissue preparation
Day 1: Whole mouse brain (2 years old, male) was fixed overnight in 4%PFA.
Day 2: Brain was washed 3x 5' in PBS + 4% Sucrose
Day2: Brain was incubated overnight in PBS + 30% Sucrose
Day3: Brain was embedded into optimal cutting medium (OCT)
Day3: Brain was cut with a cryostat in 10um thick sections and stored at -80C
Antibody staining protocol day 1
Slides with brain tissue sections were thawed 0h 15m 0s
Room temperature
Add slides to glass coplin Jar.
Wash 3x 0h 10m 0s
in PEMTx
Move slides to plastic coplin jar for antigen retrieval
Perform antigen retrieval 0h 15m 0s
85°C
Let plastic coplin jar cool down to room temperature 0h 20m 0s
Place slides back in original glass complin jar
Wash 2x 0h 10m 0s
in PEMTx
Place slides horizontally in box humidified with MQ. Use hydrophobic pen to outline tissue sections.
Add blocking buffer to the slides and incubate 1h 0m 0s
Add antibody solution (blocking buffer + 1:100 LBP110 + 1:100 p62) and incubate 4°C
Antibody staining protocol day 2
Wash slides 4x 0h 15m 0s
Incubate with secondary antibody solution in humidified box (PEMTx + 2% BSA + 1:500 secondary antibodies + 1:1000 DAPI) for 1h 0m 0s
Place slides back in coplin jar (keep in dark)
Wash 3x 0h 10m 0s
in PEMTx
Wash 2x 0h 7m 0s
in PEM
Mount slides using Prolong Gold mounting medium and store at 4°C