Catalog Number : 500-P180G
Produced from sera of goats pre-immunized with highly pure (>98%) recombinant Rat IL-1α. Anti-Rat IL-1α specific antibody was purified by affinity chromatography employing immobilized Rat IL-1α matrix.
|Application:||ELISA, Western Blot, Neutralization, Immunohistochemistry|
Anti-Rat IL-1α (BioGems Catalog #400-01A)
This antibody stained colchicine injected rat brain (including the ventricles and the CA3 region of the hippocampus) tissue. The primary antibody was incubated at 1.0 μg/ml overnight at 4˚C. This was followed by a peroxidase conjugated secondary antibody and then a fluorescein Tyramide Signal Amplification (TSA™) reagent. Optimal concentrations and conditions may vary. Information and photo are courtesy of the Tissue Profiling group, SciLifeLab Stockholm.
To yield one-half maximal inhibition [ND50] of the biological activity of Rat IL-1α (50 pg/ml), a concentration of 0.011 - 0.017 µg/ml of this antibody is required.
To detect Rat IL-1α by sandwich ELISA (using 100 μl/well antibody solution) a concentration of 0.5 - 2.0 μg/ml of this antibody is required. This antigen affinity purified antibody, in conjunction with BioGems' Biotinylated Anti-Rat IL-1α (62-001ABT) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant Rat IL-1α.
To detect Rat IL-1α by Western Blot analysis this antibody can be used at a concentration of 0.1- 0.2 µg/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant Rat IL-1α is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.