About Us
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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
Biospecimen Storage Protocol
GUIDELINE
- Depending on the intended laboratory analyses, and other considerations, specimens and their aliquots may be stored under different suitable conditions.
- Despite temperature, other storage conditions that are optimal for the preservation of specimen stability should be considered, such as endogenous hormones and others.
METHODS
- Slides, tissue blocks. Room temperature, about 18°C to 20°C, is recommended for preservation.
- Processing fresh specimens. Refrigerator, about 0°C to 4°C, is recommended for preservation.
- Short-term DNA stability. Freezer, about -0.5°C to -27°C, is recommended for preservation.
- DNA stability. Freezer, about -27°C to -40°C, is recommended for preservation.
- DNA / RNA stability. Freezer, about -40°C to -80°C, is recommended for preservation.
- Urine, blood, blood fractions (plasma, serum, etc.). Freezer, about -80°C to -130°C, is recommended for preservation.
- Storage of tissues, preservation of cellular viability. Liquid nitrogen vapor, about -130°C to -150°C, is recommended for preservation.
- Storage of living cells. Liquid nitrogen liquid phase, about -196°C, is recommended for preservation.
NOTES
- Adequate back-up storage capacity for low temperature units should be maintained. The power supply must be connected to a back-up generator system that immediately provides power during an electrical outage. Standard operating procedures and techniques for rapidly transferring material to back-up units during such emergencies should be documented.
- Adequate supply of liquid nitrogen must be maintained. Vapor phase liquid nitrogen storage is preferred over liquid phase storage, where cross-contamination of specimens may occur.
- Dry ice is frequently used as a refrigerant for shipping and emergency back-up for mechanical freezers.
- A system for maintenance and repair of storage equipment, support systems and facilities should be in place.
- All equipment should be validated before use, or following repairs that affect the instrument's accuracy or other capabilities.
- Labels for storage vessels must be capable of withstanding the required storage conditions, the label material must not deteriorate and printing must be readable or scannable after long-term storage.
RELATED PRODUCTS & SERVICES
Reference
- Vaught JB and Henderson MK. (2011). "Biological sample collection, processing, storage and information management." IARC Sci Publ. (163), 23-42.
For research use only. Not for any other purpose.