Table 1.
Attributes of Different Common Antibody Types
Antibody type | Production | Advantages | Disadvantages |
---|---|---|---|
Conventional polyclonal | Production time short and inexpensive. Require larger pure proteins as immunogens. | Recognize multiple epitopes on one antigen and can thus help amplify a signal from a target protein with low expression level. Comprises heterogeneous mixture of different IgGs; hence, higher affinity through cooperativity, and thus more resistant to rigorous washing. More tolerant of antigen variation; preferred choice for detection of denatured proteins. More stable over a broad pH and salt concentration. | Greater likelihood of cross-reactivity, high background, and immune mimicry. Batch-to-batch variability. |
Monotypic polyclonal | Production time short. Uses small peptides as immunogens; hence, easy to start from DNA sequence. | Simple production procedure. Can tailor antibodies to specific peptide epitopes. | Single epitope recognition means often lower affinity, and high background and cross-reactivity, also due to hapten-recognizing IgGs. |
Monoclonal | Production time long and expensive, requiring substantial technical skill. Procedure allows for selection of optimal antibodies. | A hybridoma is a constant, renewable source of identical antibodies; hence, increased reproducibility. Procedure allows for selection for optimal characteristics. Single specific IgG means lower background. | Often low concentration and modest affinity; hence, less rigorous washing possible. High epitope specificity means less tolerance of antigen variation or damage; thus highly susceptible to changes in pH and salt concentration. |