Cell therapy

Take chimeric antigen receptor (CAR) T-cell therapy and other cell therapy programs to the next level with tailored analytical solutions that provide actionable answers.
Evaluate lentiviral vectors and lipid nanoparticles for gene editing and understand proteome changes with a collaborative team of experts.

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Overview

The promise of cell therapy is staggering, bringing the possibility of a better life and even cures for diseases that were previously lethal. This promise requires the highest quality intermediate products, such as viral vectors, LNPs and CRISPR gene editing tools used for cell re-programming, and the need to understand the wider effects on the proteome.

Pursue improvements in medicine with a reliable partner for your analytical needs.

Workflow

Lentivirus characterization

Lentiviral vectors are complex modalities with quality that is linked to multiple attributes. User-friendly workflows let you determine viral protein profiles, including titer, genome integrity and nucleic acid impurities, on a single platform. Limitations on identifying host cell proteins can be overcome by solutions that offer the highest data quality.

Move your viral vector-based cell therapies forward with confidence.

  • Assess multiple viral vector quality attributes with a single solution
  • Determine protein profiles, titer, genome integrity and impurities based on high-quality data
  • Realize greater efficiency and productivity using a multi-faceted tabletop platform

Lentivirus characterization

Solution

Suited for:
  • Assessment of protein profiles, titer, genome integrity and purity
  • Faster method development and larger sample sets
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Lentivirus characterization

Solution

Suited for:
  • Assessment of protein profiles, titer, genome integrity and purity
  • Smaller sample sets
Request info
Request info

Featured resources

Filter:
High-precision lentivirus titer determination and protein profiling

Take control of the quality of your lentiviral vectors with high-performance solutions. Learn how to characterize proteins, determine protein profiles, and enhance your understanding of process changes with intuitive wor

Size distribution analysis of residual host cell DNA fragments in lentivirus

Remove barriers to assessing residual nucleic acids and control process-related impurities with accurate and reliable data. Characterize sizes and quantities of residual host-cell DNA for informed decision making.

Lentivirus characterization

Solution

Suited for:
  • Host cell protein ID
  • Simultaneous MS-based quantitation
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Workflow

Cell therapy proteome analysis

Information on gene inserts, regulatory regions, and nuclease sites of pDNA is important for investigational new drug (IND) submissions for viral vectors and protein therapeutics. Furthermore, poly-A tails for IVT mRNA are frequently encoded in the pDNA template and their lengths and potential heterogeneity require assessment. 

While these attributes can be analyzed with restriction fragment assays, accurate and reproducible sizing over an extended size range are challenges analytical scientists face. 

  • Achieve high-resolution, accurate and reproducible dsDNA analysis
  • Accurately determine pDNA fragment sizes from 100 to 15,000 bp
  • Assess encoded poly-A tail lengths for IVT mRNA production
  • Simplify DNA analysis with a turnkey, kit-based solution
  • Streamline data management and compliance needs through compatiblity with the Empower Chromatography Data System (CDS)

Cell therapy proteome analysis

Solution

Suited for:
  • Proteomics analysis
  • Quantitation of thousands of species
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All resources

Filter:
High-precision lentivirus titer determination and protein profiling

Take control of the quality of your lentiviral vectors with high-performance solutions. Learn how to characterize proteins, determine protein profiles, and enhance your understanding of process changes with intuitive workflows.

Size distribution analysis of residual host cell DNA fragments in lentivirus

Remove barriers to assessing residual nucleic acids and control process-related impurities with accurate and reliable data. Characterize sizes and quantities of residual host-cell DNA for informed decision making.

Associated applications

CRISPR/Cas9 analysis

Set your own schedule for CRISPR/Cas9 gene editing with innovative, intuitive analytical solutions. Unleash the potential of your Cas9 messenger RNA (mRNA), single guide RNA (sgRNA) and Cas9 proteins by understanding quality, purity and safety and assessing on/off target effects.

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Lipid nanoparticles and non-viral carriers

Expand the possibilities of drug delivery with innovative analytical solutions for lipid raw materials, LNPs and other non-viral carriers. Move beyond boundaries in structural elucidation and monitoring of analytes to estabilish confidence in the quality and stablity of your products.

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Proteomics

Confidence from discovery to translational research and beyond.

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Residual nucleic acid analysis

Optimize workflows to reliably detect and monitor process-related impurities. Ensure the safety of next-generation viral products with accurate, reproducible sizing of residual DNA and RNA and simultaneous quantitation.

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Viral vector characterization

Optimize your processes with solutions that overcome the analytical challenges of viral vector-based drugs. Take control of full and empty ratios and protein and genome profiles. Break down the boundaries of protein and post-translational modification (PTM) characterization with dedicated high-resolution workflows offering unprecedented depth.

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