Neutralization Antibody Validation*
Neutralization, or functional blocking, of proteins by antibodies is often used to study biologic function mediated by cell surface expressed proteins. For example, to study the effects of a particular cytokine on cell signaling and other biologic effects, antibodies can be used that will specifically bind and reduce the amount of free cytokine that can bind to receptors; thereby, down regulating its biologic effects. Neutralization testing is one strategy we use to validate Invitrogen antibodies for research use.
Neutralization or functional blocking can also be used as a tool to test the specificity of antibodies. The rationale behind this method is when an antibody exhibits functional blocking characteristics it is strong evidence that the antibody is binding the intended target and demonstrating that the antibody is specific to its intended target.
To determine if neutralization or a functional blocking approach is applicable for specificity testing, one has to rely on a defined system with a measurable output in order to be able to quantify the effects of the blocking function. These systems could be a motility assay, bioactivity assay, or any other measurable activity.
Neutralization/functional blocking validation data
In the example below, recombinant Red firefly luciferase generates light (bioluminescence) in the presence of luciferase substrate (left panel). The Red firefly luciferase antibody blocks RFF luciferase activity in a dose-dependent manner, resulting in decreased activity as reflected by reduced bioluminescence.
When possible, we combine blocking testing with other supporting data, like a western blot, to show that the antibody recognizes the intended protein target at the expected molecular weight (right panel). In the example, whole cell lysates from Red firefly (RFF) luciferase, Green Renilla (GR) luciferase, or untransfected 293 cells were analyzed in a western blot. As expected, the Red firefly luciferase antibody only detected its target in cells expressing the Red firefly luciferase protein. From these results we can verify that the Red firefly luciferase antibody functions as expected.
Western blot analysis of Red firefly luciferase (from the Japanese firefly Luciola cruciata). Electrophoresis was performed after loading 10 µg of whole cell lysates from untransfected (UT) and Red firefly (RFF Luc) or Green Renilla (GR Luc) luciferase transfected 293 cell lines, and 10 µL of PageRuler Plus Prestained Protein Ladder (Cat. No. 26619) onto a 4–20% Tris-HCl polyacrylamide gel. Proteins were transferred to a PVDF membrane and blocked with 5% BSA/TBST for 1 hr. The membrane was probed with a RFF luciferase polyclonal antibody (Cat. No. PA1-179) at a dilution of 1:4,000 overnight at 4°C on a rocking platform, washed in TBS-0.1% Tween-20, and probed with a prediluted goat anti–rabbit IgG HRP secondary antibody (Cat. No. 32460) at a dilution of 1:500 (20 ng/mL) for 1 hr. Membranes were washed, and chemiluminescent detection was performed using SuperSignal West Pico substrate (Cat. No. 34080)
In addition to the neutralization of biological activity for specificity testing of antibodies, blocking can be utilized in a different way to determine specificity. In these cases, the immunizing peptide, which is usually abundantly available, can be used as a method for antibody specificity verification. We routinely use this control in western blotting applications, especially when performing specificity testing of antibodies that are directed against specific phosphorylation sites.
Verifying target specificity of Invitrogen antibodies using neutralization/blocking
Invitrogen antibodies that have been verified against neutralization/blocking are indicated with a “verified specificity” symbol in search results and on relevant product pages. The data showing the verification will be provided on each product page.
For Research Use Only. Not for use in diagnostic procedures.