|Application ||WB, IHC, E|
|Preparation||Produced from sera of rabbits pre-immunized with highly pure recombinant Murine RELMβ. Anti-Murine RELMβ specific antibody was purified by affinity chromatography employing immobilized Murine RELMβ matrix.|
|WesternBlot||To detect Murine RELMβ 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 RELMβ is 1.5 - 3.0 ng/lane, under either reducing or non-reducing conditions.|
|Sandwich||To detect Murine RELMβ 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 RELMβ (61-116BT) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant Murine RELMβ.|
|Immunohistochemistry||This antibody stained 4% PFA, paraffin-embedded sections of murine cecum tissue (with positive goblet cells of a Trichuris muris infected mouse). The primary antibody was incubated at a concentration of 0.33 ng/mL overnight at 4°C and the secondary antibody was a cyanine-2 conjugated Donkey anti-Rabbit (Jackson ImmunoResearch). Heat induced antigen retrieval with a 100mM Citric Acid was used. Information and photos are courtesy of David Artis, University of Pennsylvania. Optimal concentrations and conditions may vary.|
|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 RELMβ Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
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