Waiting
Login processing...

Trial ends in Request Full Access Tell Your Colleague About Jove
Experiment
JoVE Encyclopedia of Experiments
Encyclopedia of Experiments: Immunology

A subscription to JoVE is required to view this content.

An In Vitro Artificial Activation Assay for Studying Fc Receptor Activation by Antibodies

 

An In Vitro Artificial Activation Assay for Studying Fc Receptor Activation by Antibodies

Article

Transcript

Dispense 100 microliters of resuspended natural killer cells into 1.5-milliliter tubes or a 96-well U-bottom plate, and place the cells on ice. Prepare rituximab or other antibody of interest at a concentration of 100 micrograms per milliliter.

Add 1 microliter to each tube of cells for a final concentration of 1 microgram per milliliter, and incubate the cells on ice for 30 minutes. During incubation, prepare a solution of anti-human kappa light chain antibody in media at a concentration of 50 micrograms per milliliter. The amount of antibody solution needed will be 50 microliters per cell sample.

Warm the antibody solution to 37 degrees Celsius on a heat block or in a water bath. When incubation of the cells is complete, add 1 milliliter of ice-cold media to each tube and centrifuge the cells at 135 times g and 4 degrees Celsius for 5 minutes. Wash the cells again with 1 milliliter of ice-cold media. Aspirate the supernatant after the last wash and add 50 microliters of the anti-human kappa light chain antibody solution to activate the cells. Immediately place cell samples at 37 degrees Celsius on a heat block or in a water bath and incubate them until the desired time points for analysis or other procedures.

The best way to handle multiple samples is to use a floating rack in a 37-degree water bath, which can be removed and placed on ice to stop all reactions immediately.

Read Article

Get cutting-edge science videos from JoVE sent straight to your inbox every month.

Waiting X
Simple Hit Counter