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Applications
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Cell Services
- Cell Line Authentication
- Cell Surface Marker Validation Service
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Cell Line Testing and Assays
- Toxicology Assay
- Drug-Resistant Cell Models
- Cell Viability Assays
- Cell Proliferation Assays
- Cell Migration Assays
- Soft Agar Colony Formation Assay Service
- SRB Assay
- Cell Apoptosis Assays
- Cell Cycle Assays
- Cell Angiogenesis Assays
- DNA/RNA Extraction
- Custom Cell & Tissue Lysate Service
- Cellular Phosphorylation Assays
- Stability Testing
- Sterility Testing
- Endotoxin Detection and Removal
- Phagocytosis Assays
- Cell-Based Screening and Profiling Services
- 3D-Based Services
- Custom Cell Services
- Cell-based LNP Evaluation
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Stem Cell Research
- iPSC Generation
- iPSC Characterization
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iPSC Differentiation
- Neural Stem Cells Differentiation Service from iPSC
- Astrocyte Differentiation Service from iPSC
- Retinal Pigment Epithelium (RPE) Differentiation Service from iPSC
- Cardiomyocyte Differentiation Service from iPSC
- T Cell, NK Cell Differentiation Service from iPSC
- Hepatocyte Differentiation Service from iPSC
- Beta Cell Differentiation Service from iPSC
- Brain Organoid Differentiation Service from iPSC
- Cardiac Organoid Differentiation Service from iPSC
- Kidney Organoid Differentiation Service from iPSC
- GABAnergic Neuron Differentiation Service from iPSC
- Undifferentiated iPSC Detection
- iPSC Gene Editing
- iPSC Expanding Service
- MSC Services
- Stem Cell Assay Development and Screening
- Cell Immortalization
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ISH/FISH Services
- In Situ Hybridization (ISH) & RNAscope Service
- Fluorescent In Situ Hybridization
- FISH Probe Design, Synthesis and Testing Service
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FISH Applications
- Multicolor FISH (M-FISH) Analysis
- Chromosome Analysis of ES and iPS Cells
- RNA FISH in Plant Service
- Mouse Model and PDX Analysis (FISH)
- Cell Transplantation Analysis (FISH)
- In Situ Detection of CAR-T Cells & Oncolytic Viruses
- CAR-T/CAR-NK Target Assessment Service (ISH)
- ImmunoFISH Analysis (FISH+IHC)
- Splice Variant Analysis (FISH)
- Telomere Length Analysis (Q-FISH)
- Telomere Length Analysis (qPCR assay)
- FISH Analysis of Microorganisms
- Neoplasms FISH Analysis
- CARD-FISH for Environmental Microorganisms (FISH)
- FISH Quality Control Services
- QuantiGene Plex Assay
- Circulating Tumor Cell (CTC) FISH
- mtRNA Analysis (FISH)
- In Situ Detection of Chemokines/Cytokines
- In Situ Detection of Virus
- Transgene Mapping (FISH)
- Transgene Mapping (Locus Amplification & Sequencing)
- Stable Cell Line Genetic Stability Testing
- Genetic Stability Testing (Locus Amplification & Sequencing + ddPCR)
- Clonality Analysis Service (FISH)
- Karyotyping (G-banded) Service
- Animal Chromosome Analysis (G-banded) Service
- AAV Biodistribution Analysis (RNA ISH)
- Molecular Karyotyping (aCGH)
- Droplet Digital PCR (ddPCR) Service
- Digital ISH Image Quantification and Statistical Analysis
- SCE (Sister Chromatid Exchange) Analysis
- Biosample Services
- Histology Services
- Exosome Research Services
- In Vitro DMPK Services
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In Vivo DMPK Services
- Pharmacokinetic and Toxicokinetic
- PK/PD Biomarker Analysis
- Bioavailability and Bioequivalence
- Bioanalytical Package
- Metabolite Profiling and Identification
- In Vivo Toxicity Study
- Mass Balance, Excretion and Expired Air Collection
- Administration Routes and Biofluid Sampling
- Quantitative Tissue Distribution
- Target Tissue Exposure
- In Vivo Blood-Brain-Barrier Assay
- Drug Toxicity Services
3D Models and Assays
In the past, the in vitro screening of synthetic and natural product libraries for novel anticancer agents mainly using established cancer cell lines grown as two-dimensional (2D) cultures, which exhibited a rapid, uncontrolled growth phenotype. Although cell lines are suitable for investigating the response of cells to various stimuli, cell lines acquire substantial bias and lose several characteristics of parental tumors during culture establishment and passage. In contrast, cells in primary culture would better retain the properties of the original tumor, whereas the conditions for primary culture of cancer cells are currently not optimized.
Three-dimensional (3D) growth of immortalized established cell lines or primary cell cultures is regarded as a more stringent and representative model on which to perform in vitro drug screening. 3D models possess several in vivo features of tumors and have many advantages in drug discovery applications.
As cancer therapeutics are moving toward targeted therapy, it is noted that 3D models hold the promise in finding new targets that were not apparent from traditional 2D culture studies. From the extensive platform of PDX models, Creative Bioarray provides a rich resource for the isolation of primary cells and cell lines across a range of cancer types, both solid tumors and blood cancer models, which then can be cultured into 3D models. Using our fresh frozen PDX cells established 3D models could shorten assay timelines, bridge the gap between in vitro and in vivo drug screening, possibly decreasing the use of animal models.
Advantages
Compare of 2D and 3D culture
Applications
The most important application of 3D models and assays in drug discovery is the effect evaluation of anticancer agents, such as methylcellulose clonogenic assays, soft agar clonogenic assays, and 3D tumor growth assays. More and more studies have shown the potential of 3D models in studying cancer biology and the development of personalized medicine. Creative Bioarray offers a variety of 3D models and assay systems for preclinical oncology and drug discovery research.
Study examples
Fig. 1. Four types of the structure of 3D spheroids based on the 3D cultures formed by a panel of 25 breast cancer cell lines
Quotation and ordering
If you have any special needs in establishment or application of 3D Models and Assays, please contact us for this special service. Let us know what you need and we will accommodate you. We look forward to working with you in the future.
References
- Kondo J,; Endo H,; et al. Retaining cell–cell contact enables preparation and culture of spheroids composed of pure primary cancer cells from colorectal cancer. Proc Natl Acad Sci USA. 2011, 108: 6235–6240.
- Rasheena E,; Jessica J B,; et al. Three-dimensional cell culture systems and their applications in drug discovery and cell-based biosensors. ASSAY and Drug Development Technologies. 2014, 12: 207-218.
- Salvatore Condello,; Cynthia A. Morgan,; et al. Beta-Catenin Regulated ALDH1A1 is a Target in Ovarian Cancer Spheroids. Oncogene. 2015 Apr 30; 34(18):2297-308.
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For research use only. Not for any other purpose.