• 圣淘沙名胜世界(新加坡)

    DAB Staining for GFP on Free-floating Fixed NHP Brain Tissue

    Aydin Alikaya, William Stauffer

    Published: 2024-02-17 DOI: 10.17504/protocols.io.eq2lyjy4mlx9/v1
    AI 解读
    浏览 1895

    Abstract

    This protocol details the procedure for immunohistochemical 3,3’-Diaminobenzidine (DAB) staining of free-floating fixed brain tissue sections using the avidin/biotin ABC complex to detect Green Fluorescence Protein (GFP).

    This protocol has been tested with free-floating non-human primate (NHP) brain tissue that has been fixed with 4% paraformaldehyde, cryoprotected with sucrose gradients, and cryo-sectioned 50 µm .

    Before start

    Steps

    Part I (Day 1)

    1.

    Bring tissue to Room temperature in Phosphate Buffered Saline ( PBS , pH 7.2-7.4) on an orbital shaker for 30 minutes. 0h 30m 0s

    2.

    Prepare Peroxide Solution (0.3 % H2O2) 2O2) in dH2O 2O.

    For 10mL 0.3% H2O2 2O2use:

    • 100µL 30% H2O2 2O2
    • 9900µL dH2O 2O
    3.

    Prepare Normal Goat Serum Blocking Solution in PBS .

    To 10mL PBS add:

    • 150µL Normal Goat Serum (= 3 drops of serum from Vectastain ABC-HRP Kit, Peroxidase Rabbit IgG PK-4001)
    4.

    Prepare Primary Antibody Solution (rabbit anti-GFP) at 1:10000 dilution in PBS :

    • 1µL rabbit anti-GFP (Thermo Fisher, Molecular Probes Cat# A11122, RRID:AB_221569)
    • 9999µL PBS .
    5.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    6.

    Quench endogenous peroxide in Peroxide Solution (0.3 H2O2) 2O2) on a shaker at Room temperature: 30 minutes. 0h 30m 0s

    7.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    8.

    Incubate in Normal Goat Serum Blocking Solution on a shaker at RT: 1 hour . 1h 0m 0s

    DO NOT RINSE after blocking serum.

    9.

    Incubate in Primary Antibody Solution on a shaker at 4°C . 0h 5m 0s.

    Part II (Day 2)

    10.

    Bring tissue (in the Primary Antibody Solution ) to Room temperature on a shaker ( 30 minutes ). 0h 30m 0s

    11.

    Prepare ABC Solution in PBS ( at least 30 minutes before use). 0h 30m 0s

    To 10mL PBS add:

    • 2 drops A from Vectastain ABC-HRP Kit, Peroxidase Rabbit IgG PK-4001.
    • 2 drops B from Vectastain ABC-HRP Kit, Peroxidase Rabbit IgG PK-4001.
    12.

    Prepare Secondary Antibody Solution ( 1:200 ) in PBS.

    To 10mL PBS add:

    • 150µL (= 3 drops from Vectastain ABC-HRP Kit, Peroxidase Rabbit IgG PK-4001) of Normal Goat Serum .
    • 50µL (= 1 drop from Vectastain ABC-HRP Kit, Peroxidase Rabbit IgG PK-4001) biotinylated goat anti-rabbit IgG secondary antibody .
    13.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    14.

    Incubate in Secondary Antibody Solution on a shaker at Room temperature : 30 minutes. 0h 30m 0s

    15.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    16.

    Incubate in ABC Solution on a shaker at Room temperature : 60 minutes. 1h 0m 0s.

    17.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    18.

    Prepare DAB Peroxide Substrate Solution in dH2O 2O.

    To use the Vector Labs DAB Peroxidase Substrate Kit (SK-4100):

    In 5mL dH2O 2O:

    • 2 drops Reagent 1
    • 4 drops Reagent 2
    • 2 drops Reagent 3
    • [optional] 2 drops of Reagent 4 (Nickel) if a black reaction product is desired

    Note: Mix well before use. Use immediately.

    19.

    Incubate in DAB Peroxide Substrate Solution on a shaker at Room temperature:

    - 0h 3m 0s -0h 6m 0s.

    Note: Watch the tissue closely to avoid high background staining.

    20.

    Rinse in PBS on a shaker at Room temperature: 3 x 5 minutes. 0h 5m 0s

    21.

    Mount tissue on charged glass slides in 1:8 PBS in dH2O 2O and let air dry.

    22.

    Rinse slides with dH2O 2O and let air dry (preferably in a hood).

    23.

    Coverslip clean and dry slides with Cytoseal 60 (Thermo Fisher #830-16).

    推荐阅读

    Nature Protocols
    Protocols IO
    Current Protocols
    扫码咨询