Sandwich ELISA using Anti-Human IgG1 Antibody [RM117] as the capture antibody, and Anti-Human Ig Light Chain Antibody [RM129] (Biotin) as the detection antibody, followed by an AP conjugated streptavidin.
Sandwich ELISA using Anti-Human IgG1 Antibody [RM117] as the capture antibody, 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 IgG1 Antibody [RM117] only reacted to human IgG1. No cross reactivity with Human IgG2, IgG3, IgG4, IgE, IgD, IgA, mouse IgG, rat IgG, or goat IgG. The plate was coated with 50ng/well of different immunoglobulins. 200ng/ml, 50ng/ml, or 10ng/ml of Anti-Human IgG1 Antibody [RM117] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.
A titer ELISA using Anti-Human IgG1 Antibody [RM117]. The plate was coated with different amounts of human IgG1. A serial dilution of Anti-Human IgG1 Antibody [RM117] was used as the primary antibody. An alkaline phosphatase conjugated anti-rabbit IgG as the secondary antibody.