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Antibody characterization studies: Intact mass, light chain and Heavy chain analysis
Site specific glycosylation and Post Translational Modifications (PTMs) studies, Lysine truncation, proline amidation, Critical Quality Attributes (CQA) monitoring.
Peptide mapping studies, N/C-Terminal sequencing, Di-sulphide mapping
light chain and Heavy chain analysis
Protein quantification using HPLC/UPLC
Process Characterization and efficiency evaluation
pI and molecular weight assessment studies of biomolecules
Peptide mapping analysis using UPLC/HPLC
Non-volatile excipient detection and quantification using CAD HPLC
Low molecular weight (Glatiramer Acetate analysis by SEC MALS)
Protein-DNA interaction studies
Quantitative Proteomics
Rapid glycan analysis for biopharmaceuticals
rProtein A analysis
Safety evaluation in Biological drugs
Screening of glycan – Clonal evaluation studies
SEC for purity assessment of protein and large molecules
Small molecule high throughput screening
Stability studies
Impurity analysis for biomolecules
Immunogenicity Assay
Antigen-antibody interaction
Advanced analytical characterization studies
Aggregation of proteins
Antibodies molar mass and glycosylation
Antigen-Antibody binding
Biosimilarity assessment studies
Charge variant analysis for biomolecules
Charge variants and heterogeneity analysis of complex large molecules using IEX chromatography
CQA monitoring
Cytotoxicity and Apoptosis Assay
Determination of Molecular Weight of Glycoproteins by Analytical Ultracentrifugation
ELISA Binding assay
FcRN and Fc gamma Binding studies
HCP analysis
For testing of injectables
Glycan profiling for biomolecules
Glycan quantification using FLD detector on UPLC/HPLC
Site specific glycosylation and Post Translational Modifications (PTMs) studies
Lysine truncation
proline amidation
Di-sulphide mapping
N/C-Terminal sequencing
Peptide mapping studies
Antibody characterization studies: Intact mass
Antibody Drug Conjugate (ADC) and Drug Antibody Ratio (DAR) analysis
Host Cell Protein studies for assessing process specific impurities in Biopharmaceuticals
Critical Quality Attributes (CQA) monitoring.
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