|Application ||WB, IHC, E|
|Preparation||Produced from sera of rabbits pre-immunized with highly pure (>98%) recombinant hIL-11. Anti-Human IL-11 specific antibody was purified by affinity chromatography employing immobilized hIL-11 matrix.|
|WesternBlot||To detect hIL-11 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 hIL-11 is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.|
|Sandwich||To detect hIL-11 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-Human IL-11 (60-011BT) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant hIL-11.|
|Immunohistochemistry||This antibody stained human brain stroke (including control cortex and stroke core areas) tissue. The primary antibody was incubated at 2.5 mg/ml overnight at 4˚C. This was followed by a fluorophore conjugated secondary antibody. Optimal concentrations and conditions may vary.|
Information and photo are courtesy of the Tissue Profiling group, SciLifeLab Stockholm.
|Neutralization||To yield one-half maximal inhibition [ND50] of the biological activity of hIL-11 (1.50 ng/ml), a concentration of 0.02-0.05 µg/ml of this antibody is required.|
|Formulation||A sterile filtered antibody solution was lyophilized from PBS, pH 7.2.|
|Reconstitution||Centrifuge vial prior to opening. Reconstitute in sterile water to a concentration of 0.1-1.0 mg/ml.|
|Precautions||Anti-Human IL-11 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
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