B-cell And T-Cell Epitope Mapping
With the antigen encounter, the host humoral immunity activates, which triggers the production of antibodies that are against the foreign invader protein epitopes. Immune system components recognise the epitope as antibodies, B cells and T cells. These epitopes of antigens are dependent on their structural properties, with several experimental methods existing to identify them.
Selection Of Disease-Specific Antigen Mimics
The potential of the Phage Display Antibody Library holds the capacity to identify significant peptide molecules that can mimic epitopes. The mimotopes have fewer similarities when the primary amino acids in the antigens are considered. Yet, they can elicit an identical or reasonably similar native epitope.
Selection Of Bioactive Peptides Bound To Receptors Or Proteins
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For Receptors
Membrane receptors are crucial for cell-cell biochemical, electrical signalling, vital for physiological functions. The pharmaceutical industries have been developing target-oriented drugs for membrane receptors.
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For Enzyme Inhibitors
With the diseases, pathogenesis occurs with an expression of abnormal enzymes. They serve as potential targets for developing the inhibitors, which act as the new drugs that block enzyme activities.
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Protein-Protein Interactions
Protein-protein interactions tend to regulate in cells the mechanisms that have normal physiological functions in cells. With the Phage Display Antibody Library, there is a potent method that is highly versatile for the study.
Selection Of Peptides Bound To Non-Protein Targets
The different types of bacteria tend to trigger immune responses that are protective, resulting through the cell surface. With the cell surface non-protein antigens, mainly the polysaccharides. There are many tumour antigens that are carbohydrates. The phage display technique has applications in identifying novel peptides against the RNA of interest by screening the Phage Display Antibody Library.
Selection Of Cell-Specific Peptides
Peptide phage display is the one that approaches high throughput has the overview, which has the identification of peptides. These are highly specific to the single-cell type and have the most common screening method, ‘Bioplanning’. These are put into the in-vitro against the different cell types that include every cell.
Selection Of Organ-Specific Peptides
Organ-specific peptides, isolated from the Phage Display Antibody Library, in-vivo phage adapting to the display technology, aim to discover brain vasculature that targets peptides utilising the Phage Display Antibody Library.
Development Of Peptide-Mediated Drug Delivery Systems
The physical transport barriers usually limit an anti-cancer drug’s delivery towards the tumours. These are within the tumours and have direct restrictions contributing towards the decreased therapeutic index and considerable emergence of drug resistance.
We at GeNext Genomics believe in catering to our industry research and development sectors with the most advanced Phage Display Antibody Library. With our team of expert professionals and experienced scientists at work, we assure you of the most advanced biologics at your service.
We believe in delivering high-quality biologics with utmost precision and high-level research that brings about the optimal results for research and further analysis. We believe in catering to the industry with competitive market prices.
Also Read: Biological Activities of Transmembrane TNF-α as a Ligand.