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Products
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The inner wall of PrimeSurface products are coated with our unique ultra hydrophilic polymer, which prevents a cell from adhering to the plastic surface induces a spontaneous cell spheroid formation in equal size and shape. |
Features
- Ideal tool for uniform spheroid cell culture formation
- The uniform spheroid cell culture could be effective formed due to the adhesion of cell is inhibited by our unique surface coating technique of PrimeSurface product.
- Ideal tool for differentiation study
- Inducer reagent for differentiation can be applied after EB body formation of ES cells.
- The chemical bonding of ultra-hydrophilic coating polymer on our product is stable culture surface which makes no elution of chemicals from substrate.
- Ideal for differentiation and stimulation response studies
Applications
Medical Research Institution/Laboratory
Cell Culture
For Stem Cell Research:
Induction of ES, iPS and mesenchymal stem cells differentiation by embryoid body formation.
For Drug Screening Research & Development:
An ideal product for drug response studies. Three dimension spheroid models are more physiologically relevant than two dimension monolayer model.
Specifications
| Cat. No | Product | Description | Culture Area | Volume | Qty/Pk | Qty/Cs |
|---|---|---|---|---|---|---|
| MS-90350 | PrimeSurface Dish 35 | 35 Φ × 14(H)mm | 9 cm2 | - | 5 | 50 |
| MS-90600 | PrimeSurface Dish 60 | 60 Φ × 15(H)mm | 21 cm2 | - | 10 | 120 |
| MS-90900 | PrimeSurface Dish 90 | 90 Φ × 20(H)mm | 57 cm2 | - | 10 | 50 |
| MS-90240 | PrimeSurface Plate 24F | 24wells, Flat | 1.8 cm2 | 3.4mL/well | 1 | 10 |
Storage: Room temperature.
Expiration: 2 years after production
| Cat. No | Product | Wells | Bottom | Volume | Qty/Pk | Qty/Cs |
|---|---|---|---|---|---|---|
| MS-9384U | PrimeSurface 384U | 384 | U bottom | 0.1mL | 1 | 20 |
| MS-9384W | PrimeSurface 384U White Plate | 384 | U bottom | 0.1mL | 1 | 20 |
| MS-9096VZ | PrimeSurface 96V | 96 | V bottom | 0.3mL | 1 | 20 |
| MS-9096MZ | PrimeSurface 96M | 96 | Spindle bottom | 0.2mL | 1 | 20 |
| MS-9096UZ | PrimeSurface 96U | 96 | U bottom | 0.3mL | 1 | 20 |
| MS-9096WZ | PrimeSurface 96U White Plate | 96 | U bottom | 0.3mL | 1 | 20 |
Storage: Room temperature.
Expiration: 3 years after production
Experiments
- Generation of Human iPS Cell-Derived Kidney Organoids and Their Application in Drug Discovery Research
- Stimulus effects Evaluation
- Blood-brain barrier (BBB)
- Comparison data (3D spheroid culture using HepG2 cell line)
- For Tissue engineering and Regenerative medicine
- Application example of hES cells differentiation using PrimeSurface
The uniform spheroids form spontaneously within one day for effective aggregate formation of ES cells by using PrimeSurface
3D spheroid culture using HepG2 cell line
- comparison data -
| Cell line | : | HepG2 |
|---|---|---|
| Seeding density | : | 1000 cells/well |
| Medium | : | DMEM+10%FBS |
| Culture period | : | 3 days |
| Plate | : | 96 well U plates for 3D culturing from different companies |
Number of Spheroids
Classification based on microscopic images
[Grade 1]
Single spheroid from single well
[Grade 2]
One main spheroid and one small satellite from one well
[Grade 3]
3 or more spheroids or badly deformed ones from one well
[Grade 4]
No spheroid formation
| Manufacturer | Product | Grade 1 | Grade 2 | Grade 3 | Grade 4 |
|---|---|---|---|---|---|
| Company A | Product A | 23 | 3 | 70 | 0 |
| Company B | Product B | 65 | 27 | 4 | 0 |
| Company C | Product C | 83 | 8 | 5 | 0 |
| Company D | Product D | 88 | 6 | 1 | 1 |
| Company E | Product E | 95 | 1 | 0 | 0 |
| S-BIO Sumitomo Bakelite Co., Ltd. |
PrimeSurface™ | 96 | 0 | 0 | 0 |
Values and images used in this application note is measured values at our company, not the values for guaranteeing. In addition, these data do not gurantee the product performance under any conditions.
※PrimeSurface™ has the advantage of supporting single well single spheroid formation
Radius* of Grade 1 Spheroids
| Product A** (n=23) |
Product B (n=65) |
Product C (n=83) |
Product D (n=88) |
Product E (n=95) |
PrimeSurface™ (n=96) |
|
|---|---|---|---|---|---|---|
| Ave (μm) | 225.4 | 244.4 | 254.8 | 238.7 | 261.6 | 240.4 |
| SD | 16.5 | 11.3 | 11.7 | 10.1 | 9.4 | 7.3 |
* Radius was calculated from the Day3 spheroid area, assuming that spheroid was sphere
** Data of Product A was from Day2 spheroids
Values and images used in this application note is measured values at our company, not the values for guaranteeing. In addition, these data do not gurantee the product performance under any conditions.
Box plot of Radius* of Grade 1 Spheroids (average=100)
※PrimeSurface™ has the advantage of supporting uniform spheroids formation
【PrimeSurface™ is a great tool to obtain highly reproductive data
by providing uniform spheroids in size】
For Tissue engineering and Regenerative medicine:
Regenova is a novel robotic system that facilitates the fabrication of three- dimensional cellular structures by placing cellular spheroids in fine needle arrays according to pre-designed 3D data. Followings are examples of such fabrications using S-BIO's PrimeSurface™ 96U plate and Bio 3D Printer, Regenova (Cyfuse Biomedical K.K.).; neural 3D tissue and 3D tissue with mesenchymal stem cells.
Neural 3D tissue
| Cell sources | : | hiPSC derived neural progenitor cells |
|---|---|---|
| Quantity of cells | : | 4 X 104 cells/well |
| Culture Medium | : | For neural cells |
| Maturation duration on Well Plate | : | 2 days |
| 3D structure of printed 3D tissue | : | printed with 3 X 3 X 2 |
| Quantity of spheroids used for 3D tissue | : | 18 spheroids |
| Maturation duration after 3D printing | : | Remove needles 9 days after 3D print |
Spheroid
After 3D print
3D tissue after removal of needles
3D tissue with mesenchymal stem cells
| Cell sources | : | human adipose tissue derived mesenchymal stem cells (hADSC) |
|---|---|---|
| Quantity of cells | : | 5 X 103 cells/well |
| Culture Medium | : | For MSC |
| Maturation duration on Well Plate | : | 2 days |
| 3D structure of printed 3D tissue | : | Circle shape with 48 spheroids x 10 layers |
| Quantity of spheroids used for 3D tissue | : | 480 spheroids |
| Maturation duration after 3D printing | : | Remove needles 6 days after 3D print |
Spheroid
After 3D print, from above
After 3D print, side view
3D tissue after removal of needles
Application example of hES cells differentiation using PrimeSurface
The uniform spheroids form spontaneously within one day for effective aggregate formation of ES cells by using PrimeSurface
Self-formation of neural retina tissue from the aggregate of human ES cells by using PrimeSurface MS-9096V
| Culture plate | : | PrimeSurface MS-9096V |
|---|---|---|
| Cell type | : | Human ES cells (KhES-1 strain) |
| Seeding density | : | 9,000 cells/well |
| Culture medium | : | GMEM+KSR+NEAA+2ME+ 20uM Y-27632 |
| Culture environment | : | 5%CO2, 37°C |
Data resource
- Picture a-c
Division of Human Stem Cell Technology RIKEN Center for Developmental Biology
Reference
- Self-Formation of Optic Cups and Storable Stratified Neural Retina from Human ESCs; NakanoT, Ando S, Takata N, Kawada M, Muguruma K, Sekiguchi K, Saito K, Yonemura S, Eiraku M, Sasai Y; Cell Stem Cell, 10 (6), 771-785 (2012)
Evaluation example of anticancer drug efficacy by using PrimeSurface
| Cell type | : | MCF-7 (Human breast cancer cell) |
|---|---|---|
| Anticancer drug | : | 5-Fluorouracil (5-FU) |
Data resource
Nishio Lab., Department of Genome Biology, Kinki University School of Medicine
Please check the supplemental data for more detail example of application.
References
Introduction of PrimeSurface™ Research Papers
- High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins
- Mathematical modeling of multicellular tumor spheroids quantifies inter-patient and intra-tumor heterogeneity
- Transcriptional Up-Regulation of FBXW7 by KCa1.1 K+ Channel Inhibition through the Nrf2 Signaling Pathway in Human Prostate Cancer LNCaP Cell Spheroid Model
- FSP1 is a predictive biomarker of osteosarcoma cells’ susceptibility to ferroptotic cell death and a potential therapeutic target
- Hepatocytes differentiate into intestinal epithelial cells through a hybrid epithelial/mesenchymal cell state in culture
- Anti-Mesothelin CAR-NK cells as a novel targeted therapy against cervical cancer
- Personalized Vascularized Models of Breast Cancer Desmoplasia Reveal Biomechanical Determinants of Drug Delivery to the Tumor
- Three-dimensional culture of human proximal tubular epithelial cells for an in vitro evaluation of drug-induced kidney injury
- Long-term viable chimeric nephrons generated from progenitor cells are a reliable model in cisplatin-induced toxicity
- Generation of multilineage liver organoids with luminal vasculature and bile ducts from human pluripotent stem cells via modulation of Notch signaling
- In vitro hair follicle growth model for drug testing
- Comparison of the effects of oxidative and inflammatory stresses on rat chondrocyte senescence
- Proteomics and disease network associations evaluation of environmentally relevant Bisphenol A concentrations in a human 3D neural stem cell model
- Hypoxia inducible factor-1α promotes trichogenic gene expression in human dermal papilla cells
- ASPSCR1::TFE3 orchestrates the angiogenic program of alveolar soft part sarcoma
- Enhanced chondrogenic differentiation of iPS cell-derived mesenchymal stem/stromal cells via neural crest cell induction for hyaline cartilage repair
|
Supplemental Data
Time-lapse imaging of human iPS cells spheroid (embryoid body) formation
[Culture conditions]
| Culture plate | : | PrimeSurface MS-9096V |
|---|---|---|
| Cells | : | hiPS cell (201B7: Takahashi K et al. Cell, 2007 Nov 30;131(5):861-72, iPS Academia Japan, Inc.) |
| Seeding density | : | 9,000 cells/well |
| Culture medium | : | DMEM/F12 + 20% (v/v) KSR + 1% (v/v) NEAA + L-Glutamine (2mM) + Β-Mercaptethanol (80μM) + Y-27632(30μM) |
| Culture environment | : | 5%CO2, 37°C |
Time-lapse imaging of HeLa cells spheroid formation in 96 well plat
[Culture conditions]
| Seeding density | : | 1,000 cells/well |
|---|---|---|
| Culture medium | : | MEM+10FBS 100μL/well |
| Culture period | : | 48hours |
Time-lapse imaging og HepG2 cells spheroid formation in 384 well plate
[Culture conditions]
| eding density | : | 1,000 cells/well |
|---|---|---|
| Culture medium | : | DMEM (Low Glucose) + 10%FBS 50μL/well |
| Culture period | : | 48hours |
- 2026/08/25Newsletter[S-BIO Insight] “PrimeSurface Enables High-Throughput Blood Vessel Organoid Research for Cerebral Cavernous Malformation Drug Discovery”
- 2026/08/05Newsletter[S-BIO Insight] “Announcement: S-BIO Web Seminar vol.2”
- 2026/07/28Newsletter[S-BIO Insight] “Daily Rhythms in Plasma Glycan Profiles: Normal vs. Obese Mice and the Timing of Dapagliflozin Administration”
- 2026/06/12Newsletter[S-BIO Insight] “Exosome Preparation Supported by PROTEOSAVE™: Chemical Reprogramming of MSCs for Inflammation Therapy”
- 2026/05/20Newsletter[S-BIO Insight] “Human Embryo Implantation Research Supported by STEMFULL™ Analysis and Novel Endometrial Organoid Model”
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