Polyclonal antibodies
Monoclonal antibodies
Inexpensive to produce
Expensive to produce
Technology required is low
High technology required
Skills required are low
Training is required for the technology use
Time scale is short
Time scale is long for hybridomas
Produces large amounts of non specific antibodies
Can produce large amounts of specific antibodies but may be too specific
Recognizes multiple epitopes on any one antigen
Recognizes only one epitope on an antigen
Can be batch to batch variability
Once a hybridoma is made it is a constant and renewable source and all batches will be identical
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Monoclonal antibodies are derived from a single clone of B cells and therefore are identical in structure and specificity, targeting a single epitope on an antigen. Polyclonal antibodies, on the other hand, are produced by multiple clones of B cells and recognize multiple epitopes on an antigen, resulting in a mixture of antibodies with different specificities.
Antibody molecules are held together by disulfide bonds, which are covalent bonds formed between sulfur atoms in the amino acid cysteine. These bonds help maintain the structure and stability of the antibody molecule.
A Coomassie stain is used to visualize total protein in a sample, while a western blot is used to detect specific proteins through antibody binding. Western blots are more specific and sensitive compared to Coomassie staining, as they rely on target-specific antibodies for detection.
Difference between collenchyma and chlorenchyma
Potential difference
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