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Blank control (blue): Hela (fixed with 2% paraformaldehyde (10 min), then permeabilized with 90% ice-cold methanol for 30 min on ice). Primary Antibody: Rabbit Anti-CYPA antibody (orb100498), Dilution: 1 µg in 100 µL 1X PBS containing 0.5% BSA, Isotype Control Antibody: Rabbit IgG (orange), used under the same conditions), Secondary Antibody: Goat anti-rabbit IgG-PE (white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA. |
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Sample: Cerebrum (Rat) Lysate at 40 ug, Hela (Human) Cell Lysate at 30 ug, Primary: Anti-CYPA (orb100498) at 1/1000 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 18 kD, Observed band size: 17/18 kD. |
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Sample: Lane 1: Mouse Thymus tissue lysates, Lane 2: Mouse Lymph node tissue lysates, Lane 3: Mouse Lung tissue lysates, Lane 4: Mouse NIH/3T3 cell lysates, Lane 5: Rat Thymus tissue lysates, Lane 6: Rat Lymph node tissue lysates, Lane 7: Rat Lung tissue lysates, Lane 8: Human Hela cell lysates, Lane 9: Human PANC-1 cell lysates, Lane 10: Human Molt-4 cell lysates, Lane 11: Human HUVEC cell lysates, Lane 12: Human THP-1 cell lysates, Primary: Anti-CYPA (orb100498) at 1/1000 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 18 kDa, Observed band size: 18 kDa. |
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Sample: NIH/3T3 (Mouse) Cell Lysate at 30 ug, A431 (Human) Cell Lysate at 30 ug, Primary: Anti-CYPA (orb100498) at 1/1000 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 18 kD, Observed band size: 18 kD. |
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Tissue/cell: rat brain 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 37°C for 20 min, Incubation: Anti-CYPA Polyclonal Antibody, Unconjugated (orb100498) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining. |
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Tissue/cell: rat brain 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 37°C for 20 min, Incubation: Anti-CYPA Polyclonal Antibody, Unconjugated (orb100498) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining. |