Microfluidic Chip Development Service for Cell Capture

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Background Cell Capture on Chip What We Can Offer Why Choose Us? FAQs

Creative Biolabs Microfluidic Chip Development Service for Cell Capture helps you accelerate your biological discoveries, obtain precise cell capture, and streamline high-throughput analysis through advanced microfluidic design, precision fabrication, and innovative cell capture techniques.

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Background

Cell capture enables selective extraction of individual cells or clustered populations from complex mixtures, followed by spatial immobilization of specimens for downstream analytical processes. This foundational technique serves as a cornerstone across biomedical research and diagnostic applications, facilitating single-cell profiling, cellular heterogeneity mapping, intercellular communication dynamics, pharmacological screening platforms, and circulating rare oncocyte tracking.

Cell Capture on Microfluidic Chip

Microfluidic cell capture platforms enable precise immobilization of individual cells or cellular clusters within isolated microenvironments, facilitating analysis at single-cell resolution. These engineered microsystems synergize cultivation chambers with analytical modules to detect subcellular regulatory dynamics, supporting multi-parametric cellular interrogation from isolated units to organotypic scales. Furthermore, they replicate biomimetic 3D niches for advanced culture models, permitting mechanistic studies of mechanobiological influences on cellular phenotypes. Integrated automated analytical workflows accelerate high-content phenotyping in minutes rather than traditional multi-hour protocols.

Fig 1. Microfluidic chip for single-cell protein profiling. (OA Literature)Fig 1. Microfluidic chip design and functionality for single-cell protein profiling.1

Microfluidic cellular capture methodologies are broadly categorized into active non-contact techniques and contact-based immobilization through surface modifications or hydrodynamic forces. Active approaches utilize optical, dielectrophoretic, acoustic, or magnetic field manipulation, whereas contact-based systems employ chemically induced surface adhesion or passive hydrodynamic entrapment. Primary hydrodynamic isolation subtypes include micropillar arrays, microfiltration membranes, microwell configurations, and chamber-based confinement. Compared to active methods, passive hydrodynamic techniques demonstrate enhanced operational simplicity, higher throughput efficiency, and reduced cost requirements. These systems function through inherent fluidic forces, microchannel geometry, and integrated physical barriers within the device architecture.

What We Can Offer

Creative Biolabs serves as your end-to-end collaborator in fluidic system innovation, delivering tailored systems and technical services addressing experimental and developmental objectives.

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Why Choose Us

Creative Biolabs pioneers next-generation microfluidic solutions, offering unmatched precision for cellular capture challenges. Our proprietary integration of domain expertise, advanced technological infrastructure, and partnership-driven methodologies ensures breakthrough results.

We specialize in customizable systems, high-throughput efficiency, and precision-engineered architectures that integrate seamlessly into existing laboratory ecosystems.

FAQs

Q: Which biological specimens are isolatable using your fluidic systems?
A: Our microfluidic systems enable precise retention of diverse biological specimens, spanning mammalian lineages (e.g., neoplastic populations, immunocytes, progenitor lines), microbial communities (bacterial/yeast strains), and architecturally complex constructs like 3D multicellular spheroids or histotypic organoids.
Q: How does your Microfluidic Chip Development Service enhance the precision of single-cell analysis compared to traditional methods?
A: Our methodology employs precision-engineered microenvironments to perform molecular characterization at the single-cell level. Contrasting with population-averaged measurements that obscure biological variance, this enables proteomic mapping of individual cellular units, resolving masked molecular diversity inherent to conventional ensemble-based analyses.
Q: What materials are used in the fabrication of Creative Biolabs' microfluidic chips, and are they suitable for long-term cell culture or sensitive assays?
A: Fabrication prioritizes PDMS for its optical translucency, gas diffusivity, and biocompatibility critical for viability-dependent workflows. Application-specific demands are addressed through alternative substrates: fused silica for imaging fidelity, crystalline silicon for thermal stability, or surface-engineered polymers for specialized assay integration.

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Reference

  1. Armbrecht, Lucas, et al. "Single-cell protein profiling in microchambers with barcoded beads." Microsystems & nanoengineering 5.1 (2019): 55. DOI: 10.1038/s41378-019-0099-5. Distributed under Open Access license CC BY 4.0, without modification.

For Research Use Only. Not For Clinical Use.

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