Immunohistochemistry: This antibody stained colchicine injected mouse brain (somatosensory cortex) tissue. The primary antibody was incubated at 0.5 ug/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 mRANTES (100.00 ng/ml), a concentration of 0.8-1.2 ug/ml of this antibody is required. ELISA: To detect mRANTES by sandwich ELISA (using 100 ul/well antibody solution) a concentration of 0.5-2 ug/ml of this antibody is required. This antigen affinity purified antibody, in conjunction with Biotinylated Anti-Murine RANTES (
LS-C104424) as a detection antibody, allows the detection of at least 0.2-0.4 ng/well of recombinant mRANTES. Western Blot: To detect mRANTES by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 ug/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant mRANTES is 1.5-3 ng/lane, under either reducing or non-reducing conditions.