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A free online tool for protein cleavage sites prediction with a chosen enzyme.
Calculate monoisotopic and average mass of a custom peptide or peptides predicted from a protein.
The cleavage specificities of selected enzymes.
A comprehensive and freely accessible resource of protein sequence and functional information.
Mass spectrum simulation tool for peptide/protein sequences. The number of charge can be custom defined.
An online tool predicts m/z values for SMS ions generated from selected fragmentation methods such as CID, ECD, or ETD. The ion type and maximum number of charge can be pre-defined.
PDB provides the most complete collection of information about the 3D structures of proteins, protein complexes and other biomolecules.
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Our Electron Microscopy Polyclonal Epitope Mapping (EMPEM) technology platform can quickly interrogate the immune responses against biologics. The EMPEM and cryo-EMPEM workflows allow you to study the polyclonal antibody responses against a biotherapeutics candidate. Antigen molecules bound with these antibodies can be directly isolated from the serum and subjected to high-resolution cryo-EM analysis. Detailed structural information allows the mapping of different epitopes on the biotherapeutics at single-residue and atomic resolution. The amino acid residues in these epitopes can then be engineered to reduce the immunogenicity for protein/antibody therapeutics and gene therapy viral vectors. EMPEM is also a powerful tool for mapping antibody responses to each epitope in the serum, providing immediate feedback for mechanistic evaluation of epitope-targeting. The abundance of pAbs to each epitope can also be calculated to show immune transitions over time.
For vaccine development, the elicitation of effective neutralizing antibodies (nAbs) is a primary determinant of the efficacy of a new vaccine candidate. To develop a universal vaccine against various strains of a virus, it is critical to make sure the vaccine can induce antibodies targeting broadly neutralizing epitopes. To aid in the development of more effective vaccines, NovoAb's EMPEM and cryo-EMPEM service platforms can quickly characterize the binding epitope profile of vaccine induced antibody repertoires. It can also check if the desired antibodies directed toward a specific epitope (e.g. a broadly neutralizing epitope recognized by a bnAb) are present and provide epitope-targeted antibody response quantitation in biofluids such as serum. It is applicable to vaccines against any kind of viruses, including SARS-Cov-2 coronavirus, Influenza virus, Dengue virus and others.
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