Immunohistochemical staining of human skin tissue using EXOSC10 antibody.
Immunohistochemical staining of mouse lymph tissue using EXOSC10 antibody.
Paraformaldehyde-fixed, paraffin embedded (mouse skin), Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min, Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes, Blocking buffer (normal goat serum) at 37C for 30 min, Antibody incubation with (EXOSC10) Polyclonal Antibody, Unconjugated (orb156799) at 1:200 overnight at 4C, followed by operating according to SP Kit (Rabbit) instructionsand DAB staining.
Sample: U937 (Human) Cell Lysate at 30 ug, Primary: Anti-EXOSC10 (orb156799) at 1/1000 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 101 kD, Observed band size: 103 kD.
Tissue/Cell: human skin tissue, 4% Paraformaldehyde-fixed and paraffin-embedded, Antigen retrieval: citrate buffer (0.01M, pH 6.0), Boiling bathing for 15 min, Block endogenous peroxidase by 3% Hydrogen peroxide for 30 min, Blocking buffer (normal goat serum) at 37C for 20 min, Incubation: Anti-EXOSC10, Unconjugated (orb156799) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining.
Tissue/Cell: Mouse Lymph nodes, 4% Paraformaldehyde-fixed and paraffin-embedded, Antigen retrieval: citrate buffer (0.01M, pH 6.0), Boiling bathing for 15 min, Block endogenous peroxidase by 3% Hydrogen peroxide for 30 min, Blocking buffer (normal goat serum) at 37C for 20 min, Incubation: Anti-EXOSC10, Unconjugated (orb156799) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining.
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