PrimeSurface 低吸附细胞培养板
- 产品特性
- 相关资料
- Q&A
- 参考文献
PrimeSurface 低吸附细胞培养板
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PrimeSurface 低吸附细胞培养板
PrimeSurface 低吸附细胞培养板
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PrimeSurface 低吸附细胞培养板
PrimeSurface 35mm dish
低吸附相关试剂
PrimeSurface 低吸附细胞培养板
PrimeSurface® 是采用 sumiron 公司的低吸附蛋白质处理产品(Proteosave® SS)的技术制成的低吸附细胞处理产品。使用该容器培养细胞更容易形成细胞球集落。
◆特长
● 能够简单地形成细胞集落
将细胞播种在96、384多孔板中,静置培养就能简单地得到细胞集落。
● 细胞集落大小均一
抑制细胞吸附在培养面,集落的形成率得到了提高,能够在细胞形态平整、均一的状态下培养。
● 适用于细胞分化的研究
能够将ES细胞变成胚叶体(EB体)后直接添加分化诱导试剂 。
● 适合用于使用细胞球进行抗癌剂的筛选
进行3D培养,与常规的单层培养相比培养环境更加接近生物体。
◆用途
用于再生医疗和药物研发中
◆细胞培养
● ES细胞·IPS细胞·骨髓间充质干细胞的分化诱导
● 使用细胞的3D模型进行药物研发筛选
◆产品概要
产品编号 |
产品名称 |
规格 |
培养面积 |
容量 |
包装 |
MS-9035XZ |
PrimeSurface® 培养皿35mm |
外寸35Φ×14(H)mm |
9 cm2 |
– |
5包·50/case |
MS-9060XZ |
PrimeSurface® 培养皿60mm |
外寸60Φ×15(H)mm |
21 cm2 |
– |
10包·100/case |
MS-9090XZ |
PrimeSurface® 培养皿90mm |
外寸90Φ×20(H)mm |
57 cm2 |
– |
10包·50/case |
MS-9024XZ |
Sumiron Celltight 板24F |
24孔·平底 |
1.8 cm2 |
3.4 mL/well |
1包·10/case |
注:已进行放射线灭菌 保存温度:室温 有效期:制造后两年
产品编号 |
产品名称 |
孔数 |
孔底形状 |
容量 |
包装 |
MS-9384UZ |
PrimeSurface® 384U多孔板 |
384 |
U底 |
0.1 mL |
1/包・20/case |
MS-9384WZ |
PrimeSurface® 384U白色多孔板 |
384 |
U底 |
0.1 mL |
1/包・20/case |
MS-9096VZ |
PrimeSurface® 96V多孔板 |
96 |
V底 |
0.3 mL |
1/包・20/case |
MS-9096MZ |
PrimeSurface® 96M多孔板 |
96 |
纺锤底 |
0.2 mL |
1/包・20/case |
MS-9096UZ |
PrimeSurface® 96U多孔板 |
96 |
U底 |
0.3 mL |
1/包・20/case |
MS-9096WZ |
PrimeSurface® 96U白色多孔板 |
96 |
U底 |
0.3 mL |
1/包・20/case |
注:已进行放射线灭菌 保存温度:室温 有效期:制造后两年
◆实验例子
在用球体制作工程构建三维结构体时使用了 Cyfuse 的生物3D打印机 Regenova®
Regenova® 是先进的机器人系统之一,它通过将球体固定在剑山,再按照3D设计制作出三维结构体。下面为大家介绍使用了该系统的神经三维结构体和使用了间充质干细胞的三维结构体的实验例子。
神经三维结构体
使用细胞:人iPSC来源神经前驱细胞
播种数:4×104 cells/well
培养基:神经细胞用培养基
培养板培养天数:2天
制作出的三维结构体的形状、尺寸:3×3×2
用于三维结构体的细胞块个数:18个
积层后的培养天数:9天后拔出剑山
细胞块 |
3D打印后 |
拔出剑山后的三维结构体 |
使用间充质干细胞的三维结构体
使用细胞:人脂肪组织来源间充质干细胞
播种数:5×103 cells/well
培养基:间充质干细胞用培养基
培养板培养天数:2天
制作出的三维结构体的形状、尺寸:用48个细胞块组成环状×10层
用于三维结构体的细胞块个数:480个
积层后的培养天数:6天后拔出剑山
细胞块 |
3D打印后(上面) |
3D打印后(侧面) |
拔出剑山后 |
使用 PrimeSurface® 96U 多孔板的培养例子
小鼠ES细胞培养
播种数:750 cells/well
培养基:DMEM+4.5 mg/mL Glc.
添加物:15%灭活 FCS
2 mM L-谷氨酰胺
1%非必须氨基酸
110 μM 2-巯基乙醇
培养日数:3日
没有细胞吸附在 PrimeSurface® 96U 多孔板上,也没有凌乱的细胞集落,已经形成均一。 |
|
一般市面上贩卖的漂浮培养用多孔板,细胞紧密粘附或者死亡。 |
使用PrimeSurface® 96U多孔板的细胞分化诱导实验例子
使用PrimeSurface® MS-9096V将人ES细胞集落导入自身组织化神经网膜组织
培养器:PrimeSurface® MS-9096V
使用细胞:人ES(KhES-1株)
播种密度:9000 cells/well
使用培养基:GMEM+KSR+NEAA+2ME+ 20uM Y-27632
培养条件:5% CO2,37℃
【数据提供】
・照片a)~c)
理化学研究所 发生与再生科学综合研究中心 干细胞研究支援开发室
【参考文献】
・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)
使用PrimeSurface® 进行抗癌药药效测试实验
细胞:MCF-7(人乳腺癌细胞)
试剂:5-Fluorouracil(5-FU)
【数据提供】
・近畿大学医学部 基因组生物学教室 西尾研究室
在小鼠 ES 细胞形成球体引起心肌细胞分化的过程中使用 DS Pharma Biomedical 的心肌分化毒性(发生毒性)评价试剂盒。
POCA® Hand1-EST
POCA® Hand1-EST 是一种使用 PrimeSurface,在待测物存在下的培养中将检测小鼠ES细胞的心肌分化是否正常作为标记基因活性的指标的方法。
使用细胞:小鼠ES细胞(Hand1-ES细胞)
播种数:750 cells/well
培养基:心肌分化培养基
培养板培养天数:5天
研究领域 |
使用型号 |
参考文献 |
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视网膜 研究 |
MS-9096V |
KUWAHARA, Atsushi, et al. Generation of a ciliary margin-like stem cell niche from self-organizing human retinal tissue. Nature communications, 2015, 6.: 1-15 |
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MS-9096V |
TANAKA, T., et al. Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells. Sci Rep, 2015, 5. 8344. |
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MS-9096U |
EIRAKU, Mototsugu and SASAI, Yoshiki Mouse embryonic stem cell culture for generation of three-dimensional retinal and cortical tissues. Nature protocols, 2012, 7. 1: 69-79. |
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MS-9096V |
NAKANO, Tokushige, et al. Self-Formation of Optic Cups and Storable Stratified Neural Retina from Human ESCs. Cell Stem Cell, 2012, 10. 6: 771-785. |
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MS-9096V |
GAO, Lixiong, et al. Intermittent high oxygen influences the formation of neural retinal tissue from human embryonic stem cells.Scientific Reports, 2016, 6. |
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神经科学 研究 |
MS-9096V |
MUGURUMA, Keiko, et al. Self-Organization of Polarized Cerebellar Tissue in 3D Culture of Human Pluripotent Stem Cells. Cell Reports, 2015, 10:537-550 |
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MS-9096V |
BAMBA, Y., et al. Differentiation, polarization, and migration of human induced pluripotent stem cell-derived neural progenitor cells co-cultured with a human glial cell line with radial glial-like characteristics. Biochem Biophys Res Commun, 2014, 447. 4: 683-688. |
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MS-9096 U, M or V |
MINAMINO, Yuki, et al. Isolation and Propagation of Neural Crest Stem Cells from Mouse Embryonic Stem Cells via Cranial Neurospheres. Stem cells and development, 2014, 24.2: 172-181 |
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MS-9096V |
KADOSHIMA, T., et al. Self-organization of axial polarity, inside-out layer pattern, and species-specific progenitor dynamics in human ES cell-derived neocortex. Proceedings of the National Academy of Sciences of the United States of America, 2013, 110. 50: 20284-20289. |
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MS-9096 U, M or V |
OGAWA, Yasuhiro, et al. Impaired neural differentiation of induced pluripotent stem cells generated from a mouse model of Sandhoff disease. PLoS ONE, 2013, 8. 1: e55856. |
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MS-9035X |
GOMI, Masanori, et al. Functional recovery of the murine brain ischemia model using human induced pluripotent stem cell-derived telencephalic progenitors. Brain research, 2012, 1459. 52-60. |
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MS-9096 U, M or V |
NASU, Makoto, et al. Robust formation and maintenance of continuous stratified cortical neuroepithelium by laminin-containing matrix in mouse ES cell culture. PLoS ONE, 2012, 7. 12: e53024. |
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MS-9096 U |
DANJO, T., et al. Subregional specification of embryonic stem cell-derived ventral telencephalic tissues by timed and combinatory treatment with extrinsic signals. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011, 31. 5: 1919-1933. |
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MS-9096 U |
KANEMURA, Yonehiro Development of cell-processing systems for human stem cells (neural stem cells, mesenchymal stem cells, and iPS cells) for regenerative medicine. The Keio journal of medicine, 2010, 59. 2: 35-45. |
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MS-9096 U, M or V MS-9035X, MS-9060X or MS-9090X |
FUKUSUMI, Hayato, et al. (2016). Establishment of human neural progenitor cells from human induced pluripotent stem cells with diverse tissue. Stem cells international: 1-10. |
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MS-9096 U, M or V |
RAASCH, Martin, et al. (2016). An integrative microfluidically supported in vitro model of an endothelial barrier combined with cortical spheroids simulates effects of neuroinflammation in neocortex development. Biomicrofluidics. 10: 044102. |
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MS-9096 M |
ISODA, Miho, et al. (2016). Robust production of human neural cells by establishing neuroepithelial-like stem cells from peripheral blood mononuclear cell-derived feeder-free iPSCs under xeno-free conditions. Neuroscienc Research. |
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MS-9035X, MS-9060X or MS-9090X |
BAMBA, Yohei, et al. (2016). In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations. Molecular brain. |
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MS-9096V |
SAKAGUCHI, Hideya, et al. (2015). Generation of functional hippocampal neurons from self-organizing human embryonic stem cell-derived dorsomedial telencephalic tissue. Nature communications. 6: 1-11. |
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MS-9096V |
MUGURUMA, Keiko, et al. Self-Organization of Polarized Cerebellar Tissue in 3D Culture of Human Pluripotent Stem Cells. Cell Reports, 2015, 10:537-550 |
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KAMIYA, Daisuke, et al. Intrinsic transition of embryonic stem-cell differentiation into neural progenitors. Nature, 2011, 470. 7335: 503-509. |
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心肌细胞 研究和心脏研究 |
MS-9096V |
TAKASHIMA, Yasuhiro, et al. Resetting transcription factor control circuitry toward ground-state pluripotency in human. Cell, 2014, 158. 6: 1254-1269. |
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MS-9035X |
OTSUJI, Tomomi G, et al. Dynamic link between histone H3 acetylation and an increase in the functional characteristics of human ESC/iPSC-derived cardiomyocytes. PLoS ONE, 2012, 7. 9: e45010. |
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MS-9096U |
SATOSHI, Yasuda, et al. AW551984: a novel regulator of cardiomyogenesis in pluripotent embryonic cells. Biochemical Journal, 2011, 437. 2: 345-355. |
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MS-9096U |
YASUDA, S., et al. A novel regulator of cardiomyogenesis in pluripotent embryonic cells. The Biochemical journal, 2011, 437. 2: 345-355. |
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MS-9096U |
OTSUJI, Tomomi G, et al. Progressive maturation in contracting cardiomyocytes derived from human embryonic stem cells: Qualitative effects on electrophysiological responses to drugs. Stem cell research, 2010, 4. 3: 201-213. |
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MS-9035X, MS-9060X or MS-9090X |
YAMAUCHI, Kaori, et al. Cardiomyocytes develop from anterior primitive streak cells induced by β‐catenin activation and the blockage of BMP signaling in hESCs. Genes to Cells, 2010, 15. 12: 1216-1227. |
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MS-9096V |
GUO, Ge, et al. (2016). Naive pluripotent stem cells derived directly from isolated cells of the human innercell mass. Stem Cell Reports. 6: 437-446. |
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MS-9096 U MS-9035X, MS-9060X or MS-9090X |
NOGUCHI, Ryo, et al. (2016). Development of a three-dimensional pre-vascularized scaffold-freecontractile cardiac patch for treating heart disease. The Journal of Heart and Lung Transplantation. 35: 137-145. |
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MS-9096 |
NOGUCHI, Ryo, et al. Development of a Three-Dimensional Prevascularized Scaffold-Free Contractile Cardiac Patch for Treating Heart Disease. The Journal of Heart and Lung Transplantation, 2015, |
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肝细胞 研究 |
MS-9096 U, M or V |
ISHII, Takamichi (2012). Differentiation of Human Embryonic Stem Cells into Functional Hepatocyte-Like Cells (Method). Stem Cells and Cancer Stem Cells, Volume 2, Springer: 43-49. |
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MS-9096 U, M or V |
ISHII, Takamichi et al. (2012). Hepatic Maturation of hES Cells by Using a Murine Mesenchymal Cell Line Derived from Fetal Livers.Human Embryonic and Induced Pluripotent Stem Cells, Springer: 397-403. |
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MS-9096U |
ISHII, Takamichi, et al. In vitro hepatic maturation of human embryonic stem cells by using a mesenchymal cell line derived from murine fetal livers. Cell and tissue research, 2010, 339. 3: 505-512. |
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MS-9096U |
YANAGIDA, Ayaka, et al. Liver maturation deficiency in p57 Kip2-/-mice occurs in a hepatocytic p57 Kip2 expression-independent manner. Developmental biology, 2015, |
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牙科 研究 |
MS-9035X, MS-9060X or MS-9090X |
OZEKI, Nobuaki, et al. Differentiation of Human Skeletal Muscle Stem Cells into Odontoblasts Is Dependent on Induction of α1 Integrin Expression.Journal of Biological Chemistry, 2014, 289. 20: 14380-14391. |
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MS-9096 U, M or V |
YAMAMOTO, Mioko, et al. Three-dimensional spheroid culture promotes odonto/osteoblastic differentiation of dental pulp cells.Archives of oral biology, 2014, 59. 3: 310-317. |
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生精小管 研究 |
MS-9096V |
YOKONISHI, T., et al. In Vitro Reconstruction of Mouse Seminiferous Tubules Supporting Germ Cell Differentiation. Biol Reprod, 2013, 89. (1):15: 1–6. |
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iPS细胞 生成 |
MS-9035X |
OHNISHI, Hiroe, et al. A comparative study of induced pluripotent stem cells generated from frozen, stocked bone marrow‐and adipose tissue‐derived mesenchymal stem cells. Journal of tissue engineering and regenerative medicine, 2012, 6. 4: 261-271. 1. |
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MS-9035X |
AOKI, T., et al. Generation of induced pluripotent stem cells from human adipose-derived stem cells without c-MYC. Tissue engineering. Part A, 2010, 16. 7: 2197-2206. |
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MS-9035X, MS-9060X or MS-9090X |
ODA, Y., et al. Induction of pluripotent stem cells from human third molar mesenchymal stromal cells. J Biol Chem, 2010, 285. 38: 29270-29278. |
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OHNISHI, Hiroe, et al. Generation of Xeroderma Pigmentosum-A Patient-Derived Induced Pluripotent Stem Cell Line for Use As Future Disease Model. Cellular Reprogramming (Formerly" Cloning and Stem Cells"), 2015, 17. 4: 268-274. |
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EST(胚胎干细胞试验) |
MS-9096W |
SUZUKI, N., et al. Evaluation of novel high-throughput embryonic stem cell tests with new molecular markers for screening embryotoxic chemicals in vitro. Toxicological sciences : an official journal of the Society of Toxicology, 2011, 124. 2: 460-471. |
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MS-9096U |
NAGAHORI, H., et al. (2016). Prediction of in vivo developmental toxicity by combination of Hand1-Luc embryonic stem cell test and metabolic stability test with clarification of metabolically inapplicable candidates. Toxicol Lett. 259: 44-51. |
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MS-9096U |
YU, Ruoxing, et al. (2015). A Modified Murine Embryonic Stem Cell Test for Evaluating the Teratogenic Effects of Drugs on Early Embryogenesis. PLoS ONE. 10: e0145286. |
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MS-9096W |
COZ, Florian Le, et al. (2015). Hand1-Luc Embryonic Stem Cell Test (Hand1-Luc EST): A novel rapid and highly reproducible in vitro test for embryotoxicity by measuring cytotoxicity and differentiation toxicity using engineered mouse ES cells. The Journal of Toxicological Sciences. 40: 251-261. |
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骨和软骨研究 |
MS-9096 U |
HINO, Kyosuke, et al. (2015). Neofunction of ACVR1 in fibrodysplasia ossificans progressiva. Proceedings ofthe National Academy of Sciences. 112: 15438-15443. |
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MS-9096 U, M or V |
MURATA, Daiki, et al. A preliminary study of osteochondral regeneration using a scaffold-free threedimensional construct of porcine adipose tissue-derived mesenchymal stem cells. Journal of orthopaedic surgery and research, 2015, 10. 1: 1-12. |
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MS-9096 U, M or V |
FUJIMOTO, Mai, et al. Establishment of a novel model of chondrogenesis using murine embryonic stem cells carrying fibrodysplasia ossificans progressiva-associated mutant ALK2. Biochemical and Biophysical Research Communications, 2014, 455. 3: 347-352. 1. |
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MS-9096 U |
ISHIHARA, Kohei, et al. Simultaneous regeneration of full-thickness cartilage and subchondral bone defects in vivo using a three-dimensional scaffold-free autologous construct derived from high-density bone marrow-derived mesenchymal stem cells. J Orthop Surg Res, 2014, 9. 1: 98. 1. |
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血管 研究 |
MS-9096 U MS-9035X, MS-9060X or MS-9090X |
KAGEYAMA, Tatsuto, et al. (2016). In situ crosslinkable gelatin-CMC hydrogels designed for rapid engineering of perfusable vasculatures. ACS Biomaterials Science & Engineering. |
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MS-9096U |
ITOH, M., et al. Scaffold-Free Tubular Tissues Created by a Bio-3D Printer Undergo Remodeling and Endothelialization when Implanted in Rat Aortae.PLoS ONE, 2015, 10. 9: e0136681. |
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胰岛细胞移植 |
MS-9096 U |
NAKAMURA, Kentaro, et al. (2016). Introduction to a new cell transplantation platform via recombinant peptide petaloid pieces and its application to islet transplantation with mesenchymal stem cells. Transplant International. 29: 1039-1050. |
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骨髓 研究 |
MS-9096 U |
SAYO, Kanae, et al. (2016). Fabrication of bone marrow-like tissue in vitro from dispersed-state bone marrow cells. Regenerative Therapy. 3: 32-37. |
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其它 |
MS-9035X, MS-9060X or MS-9090X |
ITO, Yoshitaka, et al. (2015). Establishment of Tsc2‑deficient rat embryonic stem cells. International journal of oncology. 46: 1944-1952. |
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MS-9096 U, M or V |
OGAWA, Yasuhiro, et al. (2015). Induced Pluripotent Stem Cells Generated from P0-Cre; Z/EG Transgenic Mice. PLoS ONE. 10: e0138620. |
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MS-9096U |
IMAI, Hiroyuki, et al. Tetraploid Embryonic Stem Cells Maintain Pluripotency and Differentiation Potency into Three Germ Layers. PLoS ONE, 2015, 10. 6: e0130585. |
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MS-9096U, MS-9096M or MS-9096V |
MITSUI, Kaoru, et al. Conditionally replicating adenovirus prevents pluripotent stem cell–derived teratoma by specifically eliminating undifferentiated cells. Molecular Therapy. Methods & Clinical Development, 2015, 2. 15026. |
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MS-9096U |
ZHOU, Yuanshu, et al. Metabolic suppression during mesodermal differentiation of embryonic stem cells identified by single-cell comprehensive gene expression analysis. Molecular BioSystems, 2015, 11. 9: 2560-2567. |
PrimSurface® 肿瘤研究参考文献
1. |
ROTEM, Asaf, et al. Alternative to the soft-agar assay that permits high-throughput drug and genetic screens for cellular transformation. Proceedings of the National Academy of Sciences, 2015, 1-6 |
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2. |
OHNISHI, Ken, et al. Plastic induction of CD133AC133-positive cells in the microenvironment of glioblastoma spheroids.International Journal of Oncology, 2014, 45.2: 581-586. |
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3. |
KODAMA, Tatsushi, et al. A Novel Mechanism of EML4-ALK Rearrangement Mediated by Chromothripsis in a Patient-Derived Cell Line. Journal of Thoracic Oncology, 2014, 9.11: 1638-1646. |
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4. |
SHIMOZATO, O., et al. Receptor-type protein tyrosine phosphatase κ directly dephosphorylates CD133 and regulates downstream AKT activation. Oncogene, 2014. |
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5. |
MIKHAIL, Andrew S., et al. Image-based analysis of the size-and time-dependent penetration of polymeric micelles in multicellular tumor spheroids and tumor xenografts. International journal of pharmaceutics, 2014, 464.1: 168-177. |
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6. |
MORI, Masamichi, et al. The Selective Anaplastic Lymphoma Receptor Tyrosine Kinase Inhibitor ASP3026 Induces Tumor Regression and Prolongs Survival in Non–Small Cell Lung Cancer Model Mice. Molecular cancer therapeutics, 2014, 13.2: 329-340. |
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7. |
AKIMOTO, Miho, et al. An inhibitor of HIF-α subunit expression suppresses hypoxia-induced dedifferentiation of human NSCLC into cancer stem cell-like cells. World, 2013, 3.4: 41-45. |
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8. |
GOUDARZI, Houman, et al. Hypoxia affects in vitro growth of newly established cell lines from patients with malignant pleural mesothelioma. Biomedical Research, 2013, 34.1: 13-21. |
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Wataru Kobayashi, et el, Culture Systems of Dissociated Mouse and Human Pluripotent Stem Cell–Derived Retinal Ganglion Cells Purified by Two-Step Immunopanning. Investigative Opthamology & Visual Science, 2018, 59.2.:776-787 [MS-9096U & MS-9090XZ] |
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Shin-Ichi Mae, et el, Generation of branching ureteric bud tissues from human pluripotent stem cells. Biochemical and Biophysical Research Communications, 2018, 495.1.:954-961 [ MS-9096 U, M or V ] |
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JunTerashima, et el, CYP1A1 and CYP1A2 expression levels are differentially regulated in three-dimensional spheroids of liver cancer cells compared to two-dimensional monolayer cultures. Drug Metabolism and Pharmacokinetics, 2018, 30.6.:434-440 [MS-9096U] |
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2017年的参考文献 (50)
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W. Wang, et al. Impaired pentose phosphate pathway in the development of 3D MCF-7 cells mediated intracellular redox disturbance and multi-cellular resistance without drug induction. Redox Biology, 2017,15.: 253-265 [MS-9096U] |
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M. Tamura, et al. Morphology-based optical separation of subpopulations from a heterogeneous murine breast cancer cell line. PLOS|One, 2017 [MS-9096V] |
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M. Sato-Nakai, et al, Metabolites of alectinib in human: their identification and pharmacological activity.Heliyon, 2017, 3.7 [MS-9096U] |
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N. Sano, et al, Enhanced axonal extension of subcortical projection neurons isolated from murine embryonic cortex using neuropilin-1. Frontiers in Cellular Neuroscience, 2017, 11.123 [MS-9096U] |
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S. Quader, et al, cRGD peptide-installed epirubicin-loaded polymeric micelles for effective targeted therapy against brain tumors. Journal of Controlled Release, 2017, 258: 56-66 [MS-9096U] |
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M. Kucinska, et al, Beyond mouse cancer models: Three-dimensional human-relevant in vitro and non-mammalian in vivo models for photodynamic therapy. Mutation Research/Reviews in Mutation Research,2017, 772: 242-262 [ MS-9096 U, M or V ] |
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S. Kessel, et al, High-Throughput 3D tumor spheroid screening method for cancer drug discovery using Celigo image cytometry. Micro- and Nanotechnologies for Quantitative Biology and Medicine, 2017, 22.4.:454-465 [MS-9096U and MS-9384U] |
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S.-i. Ito, et al, Chemically-induced photoreceptor degeneration and protection in mouse iPSC-derived three-dimensional retinal organoids. Stem Cell Research, 2017, 24.: 94-101 [MS-9090X] |
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R. Ishida, et al, The Tissue-Reconstructing Ability of Colon CSCs Is Enhanced by FK506 and Suppressed by GSK3 Inhibition. Molecular Cancer Research, 2017, 15.10 [MS-9024X] |
15. |
A. Igarashi, et al, Mast cells derived from human induced pluripotent stem cells are useful for allergen tests. Allergology International, 2017, 67.2.: 234-242 [MS-9024X] |
16. |
Y. Fujita, et al, KH-type splicing regulatory protein is involved in esophageal squamous cell carcinoma progression. Oncotarget, 2017, 8.60 [MS-9096U] |
17. |
D. Diekjürgen, et al, Polysaccharide matrices used in 3D in vitro cell culture systems. Biomaterials, 2017,141.:96-115 [ MS-9096 U, M or V ] |
18. |
E. C. Costa, et al, Spheroids formation on non‐adhesive surfaces by Liquid Overlay Technique:considerations and practical approaches. Biotechnology Journal: Special Issue: Biotech Methods andAdvances, 2017, 13.1 [ MS-9096 U, M or V ] |
19. |
Y. Bamba, et al, Visualization of migration of human cortical neurons generated from induced pluripotent stem cells. Journal of Neuroscience Methods, 2017, 289.: 57-63 [MS-9096V] |
20. |
H. Ogawa, et al, Interleukin-6 blockade attenuates lung cancer tissue construction integrated by cancer stemcells. Scientific Reports, 2017, 7.12317 [MS-9024X] |
21. |
T. Hiragi, et al, Differentiation of Human Induced Pluripotent Stem Cell (hiPSC)-Derived Neurons in Mouse Hippocampal Slice Cultures. frontiers in Cellular Neuroscience, 2017,11.143 [MS-9035X, MS-9060X, or MS-9090X] |
22. |
H. Jung, et al, Development of flexible nanocarriers for siRNA delivery into tumor tissue. International Journal of Pharmaceutics, 2017, 516.1-2.:258-265 |
23. |
M. Ikeda, et al, Dormant pluripotent cells emerge during neural differentiation of embryonic stem cells in a FoxO3-dependent manner. Molecular and Cellular Biology, 2017, 37.5 [ MS-9096 U, M or V ] |
24. |
K. Sawada, et al, Vitamin D receptor agonist VS-105 directly modulates parathyroid hormone expression inhuman parathyroid cells and in 5/6 nephrectomized rats. The Journal of Steroid Biochemistry and MolecularBiology, 2017, 167.:48-54 [MS-9096U and MS-9024X] |
25. |
H. Katayama, et al, Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon.Scientific Reports, 2017, 7 [ MS-9096 U, M or V ] |
26. |
J. Kawada, et al, Generation of a Motor Nerve Organoid with Human Stem Cell-Derived Neurons. Stem CellReports, 2017 [MS-9096V] |
27. |
M. Fukuhara, et al, A G-quadruplex structure at the 5′ end of the H19 coding region regulates H19 transcription. Scientific Reports, 2017, 7 [ MS-9096 U, M or V ] |
28. |
D. Yahia, et al, Cytotoxic activity of fumonisin B 1 in Vero cells: comparison between 2D and 3D structural microplates. Comparative Clinical Pathology, 2017, 26.3.: 561-568 [ MS-9096 U, M or V ] |
29. |
S. Tsubota, et al, PRC2-mediated transcriptomic alterations at the embryonic stage govern tumorigenesis and clinical outcome in MYCN-driven neuroblastoma. Cancer Research, 2017, 77.19 [ MS-9096 U, M or V ] |
30. |
Y. Takechi-Haraya, et al, Control of Liposomal Penetration into Three-Dimensional Multicellular. Molecular Pharmaceutics, 2017, 14.6.: 2158-2165 [ MS-9096 U, M or V |
31. |
K. Muguruma, 3D Culture for Self-Formation of the Cerebellum from Human Pluripotent Stem Cells Through Induction of the Isthmic Organizer. Organ Regeneration, 2017, 31-41 [ MS-9096 U, M or V |
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L. Li, et al, 3D High-Content Screening of Organoids for Drug Discovery, 2017 |
33. |
G. Lazzari, et al, Multicellular tumor spheroids: a relevant 3D model for the in vitro preclinical investigation of polymer nanomedicines. Polymer Chemistry, 2017, 34 [ MS-9096 U, M or V ] |
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T. Kobayashi, et al, Principles of early human development and germ cell program from conserved model systems. Nature, 2017, 546.: 416-420 [ MS-9096 U, M or V ] |
35. |
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36. |
P. Dvořáková, et al, Inhibitor-Decorated Polymer Conjugates Targeting Fibroblast Activation Protein. Journalof Medicinal Chemistry, 2017, 60.20.: 8385-8393 [ MS-9096 U, M or V ] |
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Z. Chen, et al, Tuning chemistry and topography of nanoengineered surfaces to manipulate immuneresponse for bone regeneration applications. ACS Nano, 2017, 11.5.:4494-4506 [ MS-9096 U, M or V ] |
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产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9035XZ | PrimeSurface 35mm dish PrimeSurface 35mm 培养皿 |
50个 | – | – |
MS-9060XZ | PrimeSurface® 培养皿60mm |
100个 | ||
MS-9090XZ | PrimeSurface® 培养皿90mm |
50个 | ||
MS-9024XZ | Sumiron Celltight 板24F | 10个 | ||
MS-9384UZ | PrimeSurface® 384U多孔板 |
0.1 mL | ||
MS-9384WZ | PrimeSurface® 384U白色多孔板 |
0.1 mL | ||
MS-9096VZ | PrimeSurface® 96V多孔板 |
0.3 mL | ||
MS-9096MZ | PrimeSurface® 96M多孔板 |
0.2 mL | ||
MS-9096UZ | PrimeSurface® 96U多孔板 |
0.3 mL | ||
MS-9096WZ | PrimeSurface® 96U白色多孔板 |
0.3 mL |
|
PrimeSurface 24F 多孔板(24well・平底)
PrimeSurface plate 24F
PrimeSurface 24F 多孔板(24well・平底)
◆优点・特色
● 材料本身对样品的刺激少
● 胚胎干细胞分化研究
● 巨噬细胞和树状细胞的刺激反应研究
● 上皮细胞的三维培养(维持细胞功能,观察细胞形态)
● 细胞相互作用研究
● 神经细胞分化研究
● 防止蛋白和多肽的吸附
● 维持添加物活性
● 回收细胞产物
产品编号 |
产品名称 |
尺寸 |
培养面积 |
孔容量 |
包装 |
MS-9024XZ |
PrimeSurface plate 24F PrimeSurface 24F 多孔板(24well・平底) |
24孔平底 |
1.8 cm3 |
3.4 mL |
1/包 · 10/箱 |
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9024XZ | PrimeSurface plate 24F PrimeSurface 24F 多孔板(24well・平底) |
1/包·10/箱 | – | – |
PrimeSurface 35mm 培养皿
PrimeSurface 35mm dish
PrimeSurface 35mm 培养皿
◆优点・特色
● 材料本身对样品的刺激少
● 胚胎干细胞分化研究
● 巨噬细胞和树状细胞的刺激反应研究
● 上皮细胞的三维培养(维持细胞功能,观察细胞形态)
● 细胞相互作用研究
● 神经细胞分化研究
● 防止蛋白和多肽的吸附
● 维持添加物活性
● 回收细胞产物
产品编号 |
产品名称 |
尺寸 |
培养面积 |
孔容量 |
包装 |
MS-9035XZ |
PrimeSurface 35mm dish PrimeSurface 35mm 培养皿 |
整体尺寸 35Ф×14(H)mm |
9 cm3 |
5/包·50/箱 |
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9035XZ | PrimeSurface 35mm dish PrimeSurface 35mm 培养皿 | 5/包·50/箱 | – | – |
PrimeSurface Spheroid 96U
PrimeSurface Spheroid 96U
产品编号 |
产品名称 |
孔数 |
孔底形状 |
孔容量 |
包装 |
订制 MS-9096S |
PrimeSurface Spheroid 96U |
96 |
U底 |
0.3 mL |
1/包·20/包 |
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
订制 MS-9096S | PrimeSurface Spheroid 96U | 0.3 mL |
PrimeSurface 96U 白色板
PrimeSurface 96U White plate
PrimeSurface 96U白色板
◆优点・特色
● 在一块板上就能够进行细胞聚集体形成和发光检测的研究。
● 在一块板上就能进行实验研究,因此本产品适合构建简单的实验体系。
● 应用实例:对细胞聚集体分泌的荧光酶、ATP进行活性检测。
产品编号 |
产品名称 |
孔数 |
孔底形状 |
孔容量 |
包装 |
MS-9096WZ |
PrimeSurface 96U 白色板 |
96 |
U底 |
0.3 mL |
1/包·20/箱 |
参考文献
Evaluation of novel high-throughput embryonic stem cell tests with new molecular markers
for screening embryotoxic chemicals in vitro Suzuki N, Ando S, Yamashita N, Horie N, Saito K,
Toxicological Sciences. 2011 Dec;124(2):460-71. Epub 2011 Sep 29.
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9096WZ | PrimeSurface 96U White plate PrimeSurface 96U 白色板 |
1/包·20/箱 | – | – |
PrimeSurface 96U 板
PrimeSurface 96U plate
PrimeSurface 96U 板
◆优点・特色
● 只需在 96 孔板上进行细胞的接种和静态培养,可获得细胞的三维模型。
● 不需要特殊处理或准备,就能形成尺寸均匀的细胞聚集体。
● 材料表面经化学特殊处理,无溶出液,对样品没有影响。
● 可用于分化研究、刺激反应研究等细胞对外部因素敏感的研究。
产品编号 |
产品名称 |
孔数 |
孔底形状 |
孔容量 |
包装 |
MS-9096UZ |
PrimeSurface 96U板 |
96 |
U型 |
0.3 mL |
1/包·20/箱 |
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9096UZ | PrimeSurface 96U plate PrimeSurface 96U 板 |
20个 | – | – |
PrimeSurface 96M 板
PrimeSurface 96M plate
PrimeSurface 96M 板
◆优点・特色
◆案例・应用
使用细胞:人胚胎干细胞(KhES-1株),9000 cells/well
培养基:GMEM+KSR+NEAA+2ME+ 20 uM Y-27632。
培养6天后,使用倒置显微镜进行观察。
日本理化研究所 生长•再生科学综合研究中心 井小组主任提供
产品编号 | 产品名称 | 产品规格 | 产品等级 | 备注 |
MS-9096MZ | PrimeSurface 96M plate PrimeSurface 96M 板 |
20个 | – | – |
◆PrimeSurface® 细胞球体形成原理
◆球体实时形成过程
◆PrimeSurface® 96孔板的选择
住友电木提供U型、纺锤形及V型三种底形的96孔板,进行球体形成建立肿瘤模型时,需要根据细胞的性质选择形状合适的孔板
最大容量
◆孔形状的不同会造成球体形成状态的差异
MDA-MB-453,MDA-MB-468等凝聚性较弱的细胞在底面倾斜的孔中也能形成球体!
铺板数:2×103 cells/well
培养基:RPMI + 10%FBS,37℃,5% CO2 培养日数:7日
MDA-MB-453,MDA-MB-468:人乳腺癌细胞株
近畿大学医学部基因组生物学教室 西尾研究室提供
◆产品列表
产品编号 |
产品名称 |
孔数 |
孔底形状 |
容量 |
包装 |
MS-9384UZ |
PrimeSurface® 384U plate |
384 |
U底 |
0.1 mL |
1/包·20/case |
MS-9384WZ |
PrimeSurface® 384U White plate |
384 |
U底 |
0.1 mL |
1/包·20/case |
MS-9096VZ |
PrimeSurface® 96V plate |
96 |
V底 |
0.3 mL |
1/包·20/case |
MS-9096MZ |
PrimeSurface® 96M plate |
96 |
纺锤底 |
0.2 mL |
1/包·20/case |
MS-9096UZ |
PrimeSurface® 96U plate |
96 |
U底 |
0.3 mL |
1/包·20/case |
MS-9096WZ |
PrimeSurface® 96U White plate PrimeSurface® 96U白色板 |
96 |
U底 |
0.3 mL |
1/包·20/case |
注:已进行放射线灭菌 保存温度:室温 有效期:制造后两年