Sandwich ELISA using Anti-Human IgA1 Antibody [RM124] as the capture antibody (100ng/well), and Anti-Human Ig Light Chain Antibody [RM129] (Biotin) as the detection antibody, followed by an AP conjugated streptavidin.
Sandwich ELISA using Anti-Human IgA1 Antibody [RM124] as the capture antibody (100ng/well), and Anti-Human Ig Light Chain Antibody [RM129] (Biotin) as the detection antibody, followed by an AP conjugated streptavidin.
ELISA of human immunoglobulins shows Anti-Human IgA1 Antibody [RM124] reacts only to Human IgA. Very slightly cross reacts with IgA2. No cross reactivity with Human IgG, IgM, IgD, or IgE. The plate was coated with 50ng/well of different immunoglobulins. 200ng/ml, 50ng/ml, or 10ng/ml of Anti-Human IgA1 Antibody [RM124] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.
A titer ELISA using Anti-Human IgA1 Antibody [RM124]. The plate was coated with different amounts of human IgA1. A serial dilution of Anti-Human IgA1 Antibody [RM124] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.
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