Histopathological Analysis of Renal Tissue
Corresponding Organization : Jena University Hospital
Other organizations : Queen Mary University of London, William Harvey Research Institute, Friedrich-Alexander-Universität Erlangen-Nürnberg, University Hospital Carl Gustav Carus, TU Dresden
Variable analysis
- None explicitly mentioned
- Histopathological evaluation of renal and splenic tissue using periodic acid Schiff (PAS) staining
- Staining for kidney injury molecule-1 (KIM-1), BTK, lymphocyte antigen 6 complex (Ly6g), F4-80, CD3, Ki67 and cleaved caspase-3 (CC-3) to evaluate renal sections immunohistochemically
- Staining of thrombocytes (glycoprotein-1b (GP1b)) and fibrin deposition (acid fuchsin–Orange G stain (SFOG))
- Renal tissue was fixed for at least 72 h in 5% buffered formaldehyde solution (Fischar) before dehydration and embedding in paraffin
- Sections were deparaffinized and hydrated as described previously
- Blocking of endogenous peroxidase was performed using 3% H2O2 (Carl Roth) and target retrieval solution (pH 6; Dako) was utilized for antigen retrieval in a pressure cooker
- Bovine serum albumin (BSA; Sigma Aldrich) or 20% serum (PAA Laboratories) as well as avidin and biotin solution (15 min each; Vector Laboratories) were used each to block unspecific binding sites
- Renal sections were incubated with primary antibody overnight at 4°C, further incubated with secondary antibody and with VectaStain ABC kit (Vector Laboratories) for 30 min each
- Tris(hydroxymethyl)aminomethan (TRIS) buffer (pH 7.6) containing 50 mM TRIS (Carl Roth), 300 mM sodium chloride (Carl Roth), 0.04% Tween® 20 (Sigma Aldrich) was used to wash renal sections between the staining processes
- None explicitly mentioned
- None explicitly mentioned
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