Secondary antibodies are commonly used tools alongside primary antibodies to allow for the detection and visualization of an antigen. Secondary antibodies are commonly conjugated to enzymes, fluorophores, tags, or other molecules to allow for detection or visualization. We offer a wide range of fluorophore-conjugated secondary antibodies covering the spectrum, allowing you to choose sets of antibodies with minimal spectral overlap. We offer a range of over 200 Alexa Fluor® conjugated secondary antibodies derived from various species, such as donkey, goat, and rabbit. The available products have unique absorption and emission characteristics, which correspond to common excitation wavelengths.

Secondary antibodies can be conjugated to enzymes like horseradish peroxidase (HRP) and alkaline phosphatase or to proteins like biotin to enhance primary antibody signals. HRP is a fast and stable enzyme widely used as an immunoassay detection reagent. Its high turnover rate allows secondary antibodies conjugated to HRP to produce strong signals rapidly. HRP substrates can be categorized as chromogenic (eg, DAB, TMB, or OPD), fluorogenic (eg, ADHP), or chemiluminescent (eg, ECL), depending on whether they generate a colored, fluorescent, or luminescent product. We offer a variety of HRP-conjugated secondary antibodies, including those targeting different species and isotypes, as well as fragment and pre-adsorbed forms. Our recommended HRP-conjugated secondary antibodies include goat antibodies reactive to mouse (IgG), rabbit (IgG), donkey (IgG), rat (IgG), and chicken (IgY), as well as rabbit antibodies reactive to human (IgG). These antibodies are available in various isotypes to suit different experimental needs with different conjugates or fluorophores.

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APPLICATIONS

Alexa Fluor® conjugated secondary antibodies can be used for:

HRP-conjugated secondary antibodies can be used for:

Secondary antibodies with other conjugates:

Carrier-free antibodies

FAQs

What are conjugated secondary antibodies?

Conjugated secondary antibodies are antibodies that are chemically linked (or conjugated) to a detectable marker, such as an enzyme (eg, horseradish peroxidase, HRP), a fluorescent dye, or biotin. These secondary antibodies bind to a primary antibody that is specific to a target protein, and the conjugated marker allows for the visualization or measurement of the target. The conjugated marker amplifies the signal, enabling the detection of low-abundance proteins in various techniques such as western blotting, immunohistochemistry, and flow cytometry.

How do I select a fluorescently labeled secondary antibody for flow cytometry?

To select a fluorescently labeled secondary antibody for flow cytometry, choose one that is conjugated to a fluorophore with an appropriate excitation and emission spectrum that matches your flow cytometer’s available lasers and detectors. Ensure the secondary antibody is specific to the host species of your primary antibody, and select one with minimal spectral overlap if using multiple colors for multi-parameter analysis. Additionally, consider the antibody’s sensitivity, brightness, and photostability to ensure strong, reproducible signal detection.

How do anti-mouse and anti-rabbit secondary antibodies differ?

Anti-mouse and anti-rabbit secondary antibodies differ in their specificity; anti-mouse secondary antibodies are designed to bind to mouse primary antibodies, while anti-rabbit secondary antibodies bind to rabbit primary antibodies. Each type is tailored to recognize the immunoglobulin G (IgG) or other isotypes from their respective species, enabling precise detection in experiments.

What is the role of HRP and alkaline phosphatase in secondary antibodies?

HRP and alkaline phosphatase are enzymes often conjugated to secondary antibodies to produce a signal using chromogenic substrates in detection assays. When exposed to their respective substrates, HRP catalyzes a colorimetric or chemiluminescent reaction, and alkaline phosphatase produces a colorimetric or fluorescent signal, enabling the visualization of the primary antibody binding to the target antigen.