|Application ||WB, IHC, E|
|Preparation||Produced from sera of goats pre-immunized with highly pure recombinant Murine TNF-α. Anti-Murine TNF-α specific antibody was purified by affinity chromatography employing immobilized Murine TNF-α matrix.|
|WesternBlot||To detect Murine TNF-α by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 µg/ml. When used in conjunction with compatible secondary reagents, the detection limit for recombinant Murine TNF-α is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.|
|Sandwich||To detect Murine TNF-α 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-Murine TNF-α (61-124GBT) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant Murine TNF-α.|
|Immunohistochemistry||This antibody stained colchicine injected mouse brain (hippocampus CA1 region) 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.
|Neutralization||To yield one-half maximal inhibition [ND50] of the biological activity of Murine TNF-α (0.25 ng/ml), a concentration of 0.05-0.08 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-Murine TNF-α Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
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