The following information is provided to help you decide which secondary antibody may be best for your particular application.
Secondary antibodies are directed against the species of the primary antibody. Therefore, you will need a secondary antibody that is raised in a species different than the host species of the primary antibody. For example, if your primary antibody is raised in a mouse, you will need an anti-mouse secondary antibody raised in goat, rabbit, etc.
This question is primarily important when working with monoclonal antibodies. Polyclonal antibodies, however, are typically IgG class immunoglobulins. For this reason, the secondary antibodies will mainly be an anti-IgG antibody.
Monoclonal antibodies are most commonly developed in mice and occasionally in rats, hamsters, or rabbits. For example, if the primary monoclonal antibody is mouse IgM, one would want a secondary antibody that reacts with mouse IgM (anti-Mouse IgM).
If the primary monoclonal is one of the mouse IgG subclasses, almost any anti-mouse IgG secondary antibody should bind to it. If the subclass of the primary antibody is not known, then anti-Mouse IgG F(ab) secondary antibodies may be used since they recognize most mouse immunoglobulin subclasses.
There are many classes and subclasses of human and mouse IgG(s). Choosing a secondary may be difficult. However, one common factor among these IgG(s) are the light chains (kappa and lambda). In other words, IgG, IgM, IgA, IgD and IgE all have either kappa or lambda light chains. The heavy chain, however, is class specific.
Most people prefer affinity isolated secondary antibodies because they provide the lowest amount of non-specific binding. However, in certain cases, IgG fractions may be considered, i.e. when the antigen of interest is rare or present in low abundance. In these situations high affinity antibodies are required. For example, during affinity isolation, some of the very high affinity antibodies may be removed because they bind so tightly to the affinity matrix that they are not able to be eluted.
The label is very application dependent. For immunoblotting and ELISA, enzyme-labeled secondary antibodies are the most popular. Peroxidase is economical and a more stable enzyme, in general, than alkaline phosphatase. It has also become very popular for use in chemiluminescent detection systems. Alkaline phosphatase, on the other hand, is considered more sensitive than peroxidase particularly when colorimetric detection is used.
For cell or tissue staining, alkaline phosphatase, peroxidase, or secondary antibodies conjugated to a fluorochrome may be used. Common fluorochromes are FITC, phycoerythrin, CF™ Dyes, Atto Dyes, and Quantum Red. Associated applications are immunocytochemistry/immunofluorescence, flow cytometry, or immunohistochemistry.
To generate increased amplification, a two-step biotin/avidin system may be used. Biotin binds with very high affinity to avidin, resulting in an essentially irreversible interaction. A biotinylated secondary antibody is applied first, then avidin, ExtrAvidin, or streptavidin conjugated to an enzyme or fluorochrome binds to multiple sites on the biotinylated secondary antibody, thus amplifying the signal and resulting in greater sensitivity than that achieved with an antibody-enzyme or antibody-fluorochrome conjugate alone.
Using pre-adsorbed antibodies will reduce non-specific background when working with tissues and cells. The process involves passing the secondary antibody over immobilized serum proteins from potentially cross reactive species. Therefore, if you are working with human tissues, choose a secondary antibody that has been adsorbed with human serum or human IgG.
If working with tissues or cells that have Fc receptors, choose a F(ab) or F(ab')2 fragment when possible to eliminate non-specific binding. In more detail, F(ab')2 antibody fragments are used in assay systems where the presence of the Fc region may cause problems. Samples such as lymph nodes, spleen, and peripheral blood preparations contain cells with Fc receptors (macrophages, B lymphocytes, and natural killer cells), which could bind the Fc region of intact antibodies, causing high background staining. Use of F(ab')2 fragments ensures that any antibody binding observed is not due to Fc receptors.
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