Intact MMAF ADC ELISA
Intact MMAF ADC ELISA Developed and Manufactured in the USA
Size: 1×96 wells
Sensitivity: 0.40 pg/ml
Dynamic Range: 3.3 – 270.0 ng/mL
Incubation Time: 2 hours
Sample Type: Serum, Plasma
Sample Size: 10 µL
Alternative Names: Intact Monomethyl auristatin F Antibody Drug Conjugate, Intact MMAF Antibody Drug Conjugate, Intact Monomethyl auristatin F ADC
For Research Use Only
Assay Principle
The Intact MMAF ADC ELISA is designed, developed and produced for the quantitative measurement of antibody MMAF conjugate in serum or plasma. The assay utilizes the sandwich immunoassay technique with an antibody that binds to MMAF. Briefly, a mouse monoclonal antibody specific to MMAF is coated onto a microtiter plate. In the assay system, the assay calibrators, controls and test specimen are added to this microtiter plate. During the first incubation period, the anti-MMAF monoclonal antibody captures the MMAF-Antibody Conjugate of calibrators, controls and test samples. Unbound proteins are washed away with a wash step. A HRP (horseradish peroxidase) conjugate anti-human IgG tracer antibody is added to each well of the microtiter plate. After the second incubation, a “sandwich” immunocomplex of “Anti-MMAF antibody – MMAF Antibody Conjugate – HRP-conjugated anti-human IgG antibody” is formed and attached to the wall of the plate. The unbound HRP-conjugated antibody is removed in a subsequent washing step. For the detection of this immunocomplex, each well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the immunocomplex bound to MMAF Antibody Conjugate on the wall of the microtiter well is directly proportional to the amount of MMAF Antibody Conjugate level in the sample.
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