![]() Monoclonal antibody production via the hybridoma method starts with the same immunization protocol used for polyclonal antibodies. The difference in the specificity of polyclonal antibodies and monoclonal antibodies. These issues are often addressed by cross-adsorbing (ie, further purifying) the polyclonal antibody mixture to remove antibodies with unwanted binding characteristics, often against similar antigens in particular species.įigure 2. ![]() Polyclonal antibodies can also exhibit cross-reactivity and lack of specificity because of a higher risk of binding to other proteins with similar sequences. However, the disadvantages to their use are that they are limited in supply, and batch-to-batch variation is higher than with monoclonal antibodies. So, they can produce a strong signal against the target antigen in their relevant application and are not biased against a single epitope. Polyclonal antibodies consist of a mixture of antibodies representing the natural immune response to an antigen. The resulting immune-sera (a blood portion containing the antibodies) can be used in its crude form, or the antibodies can be isolated by affinity purification. Immunizations of the same antigen are repeated at intervals of several weeks to increase the number and affinity of antigen-specific antibodies within the animal. Polyclonal antibody production typically starts with immunizing an animal with the target antigen to stimulate an immune response, involving the production of antigen-specific antibodies by the animal's B cells (Fig. Polyclonal antibodies represent a heterogeneous mix of antibodies, with each antibody recognizing different epitopes of a particular antigen. Overview of the benefits and limitations of monoclonal, polyclonal, and recombinant monoclonal antibodies and how they are produced.
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