Oct 08, 2021
IHC AD neuropathology protocol
- Christiana Bjorkli1
- 1The Norwegian University of Science and Technology
- Sandvig lab
Protocol Citation: Christiana Bjorkli 2021. IHC AD neuropathology protocol . protocols.io https://dx.doi.org/10.17504/protocols.io.btbmnik6
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it’s working
Created: March 13, 2021
Last Modified: October 08, 2021
Protocol Integer ID: 48205
Keywords: ihc ad neuropathology protocol, implanted transgenic mice, immunohistochemical processing, ad neuropathology, transgenic mice for characterization, implanted animal
Abstract
Immunohistochemical processing was conducted on tissue from chronically implanted animals, as well as non-implanted transgenic mice for characterization of AD neuropathology.
Troubleshooting
Day 1 fluorescent IHC
Heat-induced antigen retrieval on all tissue at 60 °C for 2 hours in phosphate buffer (PB).
Wash sections 3 x 10min in PB containing 0.2 % Triton X-100 (PBT+).
Block sections using 5 % normal goat serum in PBT+ for 1 hour.
Incubate sections with the primary antibodies Iba1 (1:1000; ab15690, Abcam, Cambridge, UK), McSA1 (1:1000; MediMabs, Montreal, Canada; characterization), and Aβ42 (1:1000; IBL America, Minnesota, USA; characterization) in PBT+ for 4 hours at 4 °C .
Day 1 DAB
Heat-induced antigen retrieval on all tissue at 60 °C for 2 hours in phosphate buffer (PB).
Wash in PB for 2x 10 minutes.
Permeabilize with 0.5 % Triton‐X‐100 in Tris‐buffered saline (TBS‐Tx; 50 mm Tris, 150 mm NaCl, pH 8.0) for 10 minutes.
Block with 10 % normal goat serum in TBS‐Tx for 30 minutes.
Incubate with the primary antibody (AT8, 1:1000) in TBS‐Tx overnight at 4 °C
Day 2 fluorescent IHC
Wash sections for 3 x 10 minutes with PBT.
Incubate sections with Alexa Fluor 546 to visualize Iba1 and McSA1, and Alexa Fluor 488 to visualize Aβ42, for 2 hours at room temperature, protected from light.
Wash sections for 10 minutes with 4 ′, 6-diamidino-2-fenylindol (DAPI; 1:10 000; Sigma-Aldrich, Saint-Louis, MO, USA) and PB, followed by 3 washes for 10 minutes with PB.
Day 2 DAB
Wash sections with TBS‐Tx for 3 × 10 minutes.
Incubate with a biotinylated goat anti‐mouse secondary antibody (1:500; Sigma‐Aldrich, St Louis, MO, USA) in TBS‐Tx for 90 minutes.
Wash sections for 3 x 10 minutes with TBS‐Tx.
Incubate with ABC (Vectastain ABC kit, Vector Laboratories, Burlingame, CA, USA) for 90 minutes.
Wash with TBS‐Tx for 3 x 10 minutes.
Wash with Tris‐HCl for 2 × 5 minutes.
Incubate tissue with 0.67 % diaminobenzidine (DAB) and 0.024 % H2O2 for 10 minutes before a final wash with Tris‐HCl (2 × 5 minutes).
Mounting sections
Mount tissue on cut edge frosted glass slides (VWR International, Radnor, PA, USA) with Tris-HCl and leave to dry for at least 4 hours on a 38 °C heating plate, protected from light.
Place mounted tissue in Xylene (VWR International, Radnor, PA, USA) for at least 5 minutes for defatting and to remove excess water from the tissue, and then coverslip with Entellan (VWR International, Radnor, PA, USA) containing Xylene.
Leave the mounted tissue to dry overnight, protected from light.