Sandwich ELISA using Anti-Human IgM Antibody [RM121] as the capture antibody (100ng/well), and Anti-Human Ig Light Chain Antibody [RM129] (Biotin) as the detection antibody, followed by an alkaline phosphatase conjugated streptavidin.
Sandwich ELISA using Anti-Human IgM Antibody [RM121] as the capture antibody (100ng/well), and Anti-Human Ig Light Chain Antibody [RM129] (Biotin) as the detection antibody, followed by an alkaline phosphatase conjugated streptavidin.
ELISA of human immunoglobulins shows Anti-Human IgM Antibody [RM121] reacts only to human IgM. There is no cross reactivity with Human IgG, IgE, IgD, or IgA. The plate was coated with 50ng/well of different immunoglobulins. 200ng/ml or 50ng/ml of Anti-Human IgM Antibody [RM121] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.
A titer ELISA using Anti-Human IgM Antibody [RM121]. The plate was coated with different amounts of human IgM. A serial dilution of Anti-Human IgM Antibody [RM121] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.
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