Protocol: ADA Bridging ELISA for Use with Anti-Benralizumab Antibody

Protocol: ADA Bridging ELISA for Use with Anti-Benralizumab Antibody

Protocol: ADA Bridging ELISA for Use with Anti-Benralizumab Antibody

Protocol: ADA Bridging ELISA for Use with Anti-Benralizumab Antibody

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Anti-Drug Antibody (ADA) Bridging ELISA: For Use with Anti-Benralizumab Monoclonal Antibodies Catalog HCA426, HCA427, and HCA428

This method provides a procedure for generating an ADA ELISA standard curve with Anti-Benralizumab Antibodies, HCA426, HCA427, or HCA428, using benralizumab antibody for capture and detection. The method should always be used in conjunction with product and batch-specific information provided with each vial (see product datasheets). This protocol will need to be adjusted for use with different detection methods and immunoassay technology platforms.


Reagents

BSA (Sigma-Aldrich, A7906)
HISPEC Assay Diluent (BUF049)
Human Serum (Sigma-Aldrich, H4522)
LYNX Rapid HRP Antibody Conjugation Kit® (LNK001P-LNK006P)
PBS
136 mM NaCl
2.68 mM KCl
8.1 mM Na2HPO4
1.46 mM KH2PO4
PBST
PBS with 0.05% Tween 20 (Merck Millipore, 817072)
QuantaBlu Fluorogenic Peroxidase Substrate (Thermo Fisher Scientific, 15169)

Materials

384-well microtiter plate, black, square flat-bottom wells, for example, Black 384-Well Immuno Plates (Thermo Fisher Scientific, 460518)
Fluorescence plate reader
96-well plates can be used instead of 384-well plates (black, flat-bottom wells), for example, Black 96-Well Immuno Plates (Thermo Fisher Scientific, 437111). For the 96-well format, use 100 µL (instead of 20 µL) of antigen, antibodies, or substrate and 300 µL for the blocking step.

Method

  1. Prepare the detection antibody: conjugate benralizumab antibody using a LYNX Rapid HRP Antibody Conjugation Kit.
  2. Prepare the unconjugated benralizumab capture antibody at 1 µg/mL in PBS. Coat the required number of wells of a 384-well microtiter plate with 20 µL per well of the prepared benralizumab, and incubate overnight at 4°C.
  3. Wash the microtiter plate five times (5x) with PBST.
  4. Block the microtiter plate by adding 100 µL 5% BSA in PBST to each well, and then incubate for 1 hr at RT.
  5. Wash the microtiter plate 5x with PBST.
  6. For the standard curve, prepare a dilution series of the Anti-Benralizumab Antibody HCA426 (AbD60095ia), HCA427 (AbD59975ia), or HCA428 (AbD60166ia) in 10% human serum in PBST in triplicate. Final concentration of anti-benralizumab antibody should cover the range from 0.1 ng/mL to 10,000 ng/mL. Include a zero anti-benralizumab antibody concentration as the background value.
  7. Add 20 µL of anti-benralizumab antibody dilution per well (in triplicate for each standard recommended) and incubate for 1 hr at RT.
  8. Wash the microtiter plate 5x with PBST.
  9. To each well add 20 µL HRP-conjugated benralizumab diluted to 2 µg/mL in HISPEC Assay Diluent and incubate for 1 hr at RT.
  10. Wash the microtiter plate 10x with PBST.
  11. Add 20 µL QuantaBlu Fluorogenic Peroxidase Substrate to each well and measure the fluorescence after 30 min.