Abbexa
 |
||||||||||||||||||||||||||||||
Abbexa is a dedicated worldwide supplier of biological tools for the life science, pharmaceutical and biotechnology research and development sectors. Abbexa provides the scientific community with primary antibodies, secondary antibodies, proteins, ELISA kits and enzymes as well as other kits and tools designed for use in research. Abbexa also offers custom protein, peptide and antibody production services to meet customer requirements. Abbexa is committed to providing scientists and researchers with the best customer experience and high-quality products. Abbexa’s mission is to offer unrivalled expertise and outstanding quality laboratory consumable products, striving to consistently improve. Please do get in touch with any comments regarding the website, service, products, or anything else.
Learn more :
Website : www.abbexa.com
| ||||||||||||||||||||||||||||||
Fragmented Antibodies
Secondary antibodies are antibodies that bind to primary antibodies or antibody fragments.
Fragmented secondary antibodies are antibodies that have been enzymatically digested to remove the Fc region of the antibody, leaving only the antigen-binding Fab or F(ab')2 fragments.
These fragments are monovalent or divalent, respectively, and can be used to block endogenous immunoglobulins on cells, tissues, or other surfaces, and to block the exposed immunoglobulins in multiple labeling experiments using primary antibodies from the same species. They can also be used to label primary antibodies prior to incubation with the experimental sample. The advantages of using fragment secondary antibodies include eliminating non-specific binding between Fc portions of antibodies and Fc receptors on cells, facilitating better antigen penetration into tissue, and reducing background from primary antibody binding in double staining experiments.
The advantages of using Fab fragment secondary antibodies include:
- Eliminating non-specific binding between Fc portions of antibodies and Fc receptors on cells, which is particularly important when working with live cells.
- Facilitating better antigen penetration into tissue, which is important for immunohistochemistry (IHC) experiments.
- Reducing background from primary antibody binding in double staining experiments.
- Allowing for direct conjugation to detectable labels through their sulfhydryl groups, ensuring that the active binding site of the antibody is not affected.
