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![SDS-Page: Equine IgM Isotype Control [NBP1-96970] - SDS PAGE Results Equine IgM isotype control. Lane 1: Horse IgM Reduced 1X. Lane 2: Opal Prestained Molecular Weight Marker. Lane 3: Horse IgM Non-Reduced 1X. 4-20% Gel, Coomassie Stained.](http://images.novusbio.com/fullsize/Equine IgM Isotype Control-SDS-Page-NBP1-96970-img0002.jpg "SDS-Page: Equine IgM Isotype Control [NBP1-96970] - SDS PAGE Results Equine IgM isotype control. Lane 1: Horse IgM Reduced 1X. Lane 2: Opal Prestained Molecular Weight Marker. Lane 3: Horse IgM Non-Reduced 1X. 4-20% Gel, Coomassie Stained.")
![ELISA: IgM Antibody (RM109) - Azide and BSA Free [NBP3-25956] - A titer ELISA of mouse IgM. The plate was coated with different amounts of mouse IgM. A serial dilution of RM109 was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.](http://images.novusbio.com/fullsize/nbp3-25956_rabbit-igm-mab-rm109-azide-and-bsa-free-22620242311046.jpg "ELISA: IgM Antibody (RM109) - Azide and BSA Free [NBP3-25956] - A titer ELISA of mouse IgM. The plate was coated with different amounts of mouse IgM. A serial dilution of RM109 was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.")
![ELISA: IgM Antibody (RM109) - Azide and BSA Free [NBP3-25956] - ELISA of mouse immunoglobulins shows RM109 reacts to mouse IgM; no cross reactivity with IgG1, IgG2a, IgG2b, IgG3, IgA, IgE, human IgG, rat IgG, or goat IgG. The plate was coated with 50 ng/well of different immunoglobulins. 200 ng/mL, 50 ng/mL, or 10 ng/mL of RM109 was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.](http://images.novusbio.com/fullsize/nbp3-25956_rabbit-igm-mab-rm109-azide-and-bsa-free-22620242311029.jpg)