Digital Densitometry
Method Introduction
Digital densitometry is an advanced analytical technique used to quantify the density of samples on electrophoretic gels or membranes. By measuring the optical density of stained bands, this method provides accurate and reproducible data on the concentration and purity of proteins, nucleic acids, and other biomolecules. Digital densitometry is a vital tool for assessing the quality and consistency of biopharmaceutical products throughout the development process.
Applications
Digital densitometry is extensively used in various stages of biopharmaceutical development and manufacturing. Key applications include:
- Quantifying protein concentration and purity in electrophoretic gels.
- Evaluating the consistency and quality of recombinant protein production.
- Supporting the characterization of nucleic acids in gene therapy products.
- Performing comparative studies between biosimilars and innovator drugs.
- Assessing stability studies’ results by monitoring band intensity changes over time.
Quality and Biosafety Level
We provide all our analytical services with the highest quality standards. Experienced scientists carry out each project, and a scientific reviewer comprehensively checks every report or data presentation.
We offer this technology with the following quality and biosafety levels:
R&D level
We offer this method under R&D. Our GRP system assures the highest-quality research standards.
Up to biosafety level 2
This method can be applied to nucleic acids, viruses, cells, viral vectors, including lentiviruses and more.
Analytical Method Development, Qualification and Validation
For common sample types, we can often apply standardized methods with little setup effort. However, when needed, our experienced analytical experts create or optimize custom methods tailored to your active pharmaceutical ingredient, product type and development phase.
Talk to Our Experts or Request a Quote
Our expert team is ready to answer your questions and guide you to the services best suited to your program’s modality, stage and challenge. If your needs are well-defined, we’ll begin the quotation process.