|Application ||WB, IHC, E|
|Preparation||Produced from sera of rabbits immunized with highly pure recombinant Rat IP-10. Anti-Rat IP-10 specific antibody was purified by affinity chromatography employing an immobilized Rat IP-10 matrix.|
|WesternBlot||To detect Rat IP-10 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 IP-10 is 1.5 - 3.0 ng/lane, under either reducing or non-reducing conditions.|
|Sandwich||To detect Rat IP-10 by sandwich ELISA (using 100μl/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 IP-10 (62-062BT) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant Rat IP-10.|
|Immunohistochemistry||This antibody stained colchicine injected rat brain (including the caudate putamen) tissue. The primary antibody was incubated at 0.25 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 Rat IP-10 (100 ng/ml), a concentration of 5.0-10.0 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-Rat IP-10 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
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