- You are here: Home
- Resources
- Explore & Learn
- Exosome
- Collection of Exosome Samples and Precautions
Support
-
Cell Services
- Cell Line Authentication
- Cell Surface Marker Validation Service
-
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
-
Stem Cell Research
- iPSC Generation
- iPSC Characterization
-
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
-
ISH/FISH Services
- In Situ Hybridization (ISH) & RNAscope Service
- Fluorescent In Situ Hybridization
- FISH Probe Design, Synthesis and Testing Service
-
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
-
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
Collection of Exosome Samples and Precautions
Exosomes, small extracellular vesicles released by cells, have gained significant attention in the field of biomedical research due to their potential as carriers of therapeutic cargo. To harness their therapeutic potential, it is crucial to collect exosome samples from various biological fluids and ensure the quality and integrity of the isolated exosomes.
Cell Supernatant
The selection of cell culture supernatant as the experimental material for the isolation of exosomes will not have the problem of sample size limitation like blood samples, etc., and it is easy to operate and centrifuge directly. However, in the process of cell culture needs to pay attention to the problem of contamination, culture time, and cell mortality. As with all cellular experiments, no contamination is allowed during the culture process.
Saliva
Saliva has emerged as a promising source of exosomes due to its non-invasive and easy collection procedure. To collect exosomes from saliva, several methods can be employed. One approach involves collecting saliva using specialized collection devices or tubes to prevent contamination. Another method involves the use of specialized filter-based devices that enable size-based separation of exosomes from other components in saliva.
Blood
Blood contains a rich source of exosomes that can be utilized for diagnostic and therapeutic purposes. The most common method is differential ultracentrifugation. The process involves carefully collecting blood using appropriate anticoagulants, such as EDTA or citrate, to prevent coagulation
Urine
In the sampling of urine, apart from the effects of gender, age, eating, etc., there is a special point which is the freshness of the urine. This freshness refers to how long the urine has been in the bladder.
Cerebrospinal Fluid
Cerebrospinal fluid (CSF) is a specialized fluid that surrounds the brain and spinal cord, and it has the potential to provide valuable insights into neurological diseases. The difficulties faced in cerebrospinal fluid studies are mainly in the acquisition of samples and the low abundance of exosomes in the samples. The solution to this problem is the purchase of commercially normal samples.
Precautions in Sample Collection
During the collection of exosome samples, several precautions need to be taken to ensure reliable and high-quality samples. These considerations include but are not limited to, the following.
- Using appropriate collection containers and tubes that are sterile and free from contaminants.
- Employing aseptic techniques during sample collection to prevent contamination with microbes or other external particles.
- Properly handling and storing collected samples to maintain the integrity of exosomes. This includes avoiding repeated freeze-thaw cycles, minimizing exposure to light, and storing samples at appropriate temperatures.
- Using suitable anticoagulants or preservatives, such as EDTA or citrate, depending on the sample type, to prevent coagulation or degradation of exosomes.
- Following specific protocols and guidelines provided by regulatory authorities or scientific organizations for sample collection to ensure consistency and reproducibility.
Creative Bioarray Relevant Recommendations
- Creative Bioarray provides the best quality lyophilized exosome standards and fluorescent exosome standards obtained from several biological samples, including hundreds of different cell lines, plasma, serum, saliva, and urine as well as other bio-fluids.
- We have developed quality exosome isolation tools with optimized conditions to help our customers obtain pure exosomes with a higher yield, including exosome isolation immune beads, exosome isolation immune plates, exosome isolation kits, exosome isolation reagents, and exosome size exclusion columns.
For research use only. Not for any other purpose.