Cell E&G 是一家专注于高端细胞培养耗材和高分辨率显微成像产品研发与生产的企业，公司主要面向细胞生物学、分子生物学、干细胞研究、神经科学、肿瘤学及生物医学成像等领域，为全球科研机构、高校实验室、生物技术企业及制药公司提供高品质细胞培养耗材。Cell E&G 采用德国光学玻璃、无毒医用级粘接材料及 γ 射线灭菌工艺生产产品，确保产品具有优异的光学性能、生物相容性和批间一致性，可满足共聚焦显微镜、活细胞成像、荧光显微镜、超分辨率显微镜及高内涵筛选（HCS）等应用需求。其产品以高平整度、低自发荧光、优异透光率和稳定的细胞培养性能而受到科研用户广泛采用。
更多产品信息及报价，请联系我们的销售人员 18648182152（微信同号）
◆ Cell E&G产品线
● 玻底培养皿：采用德国进口 #0 或 #1.5 光学盖玻片与高透明聚苯乙烯培养皿结合制造，具有极高的透光率和优异的平整度，可有效降低背景荧光并提升显微成像质量。产品包括 35 mm、50 mm 等多种规格以及不同玻底直径（如 13 mm、18 mm），适用于共聚焦显微镜、倒置荧光显微镜、TIRF、超分辨率显微镜及活细胞实时成像。
● 玻底多孔培养板：产品线包括 6 孔、12 孔、24 孔、48 孔及 96 孔玻底培养板，每个培养孔均配备高品质德国光学玻璃底部，可实现多个样品的同步培养和高分辨率成像。3. Glass 玻底腔室载玻片：该系列采用光学玻璃与细胞培养腔室一体化设计，提供单孔、多孔等多种规格，可直接完成细胞培养、固定、染色及显微观察，无需额外转移样品，有效减少实验误差和细胞损失。
● 标准培养皿：Cell E&G 提供多种规格的标准培养皿，包括 12 × 22 mm 和 35 mm 系列，可选择无玻璃底、18 mm 开孔、18 mm 培养孔以及配备 #0 或 #1.5 光学盖玻片等不同配置，以满足普通细胞培养、显微观察及特殊实验需求。这些培养皿采用无细胞毒性材料制造，并经过 γ 射线灭菌，可直接用于哺乳动物细胞培养和后续显微分析。
◆ Cell E&G产品列表
| 品名（英文） | 货号 | 规格 | 中文名称 |
| 35mm Glass Bottom Dish | GBD00001-200 | 35 mm，13 mm孔，#0 German cover glass，200个/盒 | 35mm玻底培养皿（13mm孔，0号盖玻片） |
| 35mm Glass Bottom Dish | GBD00002-200 | 35 mm，13 mm孔，#1.5 German cover glass，200个/盒 | 35mm玻底培养皿（13mm孔，1.5号盖玻片） |
| 35mm Glass Bottom Dish | GBD00003-200 | 35 mm，18 mm孔，#0 cover glass，200个/盒 | 35mm玻底培养皿（18mm孔，0号玻片） |
| 35mm Glass Bottom Dish | GBD00004-200 | 35 mm，18 mm孔，#1.5 cover glass，200个/盒 | 35mm玻底培养皿（18mm孔，1.5号玻片） |
| 35mm Petri Dish | PDH00001-200 | 35mm，13mm hole，无盖玻片，200个/盒 | 35mm细胞培养皿（13mm孔） |
| 35mm Petri Dish | PDH00002-200 | 35mm，18mm hole，无盖玻片，200个/盒 | 35mm细胞培养皿（18mm孔） |
| 12×22mm Petri Dish | PDP00001-20 | 12×22mm，18mm孔，无盖玻片，20个/盒 | 小型培养皿（无玻片） |
| 12×22mm Petri Dish | PDP00002-20 | 12×22mm，18mm孔，#1.5盖玻片，20个/盒 | 小型玻底培养皿 |
◆ Cell E&G参考文献
47. Kourouklis A et al. "Substrate stiffness and matrix composition coordinately control the differentiation of liver progenitor cells", Biomaterials (2016).
Paper Link
46. Márkus R et al. "Multinucleated Giant Hemocytes Are Effector Cells in Cell-Mediated Immune Responses of Drosophila", Journal of Innate Immunity (2015).
Paper Link
45. Li H et al. "Extending prematuration with cAMP modulators enhances the cumulus contribution to oocyte antioxidant defence and oocyte quality via gap junctions", Human Reproduction (2016).
Paper Link
44. Fang Z et al. "Long non-coding RNA MALAT-1 modulates metastatic potential of tongue squamous cell carcinomas partially through the regulation of small proline rich proteins", BMC Cancer (2016).
Paper Link
43. Shashikanth N et al. "Kinetic Measurements Reveal Enhanced Protein-Protein Interactions at Intercellular Junctions", Scientific reports (2016).
Paper Link
42. Razali W et al. "Wide-field time-gated photoluminescence microscopy for fast ultrahigh-sensitivity imaging of photoluminescent probes", Journal of Biophotonic (2016).
Paper Link
41. Ganguly A et al. " Perturbation of nucleo-cytoplasmic transport affects size of nucleus and nucleolus in human cells", Febs Press (2016).
Paper Link
40. Liang D et al. "The autophagy inhibitor chloroquine targets cancer stem cells in triple negative breast cancer by inducing mitochondrial damage and impairing DNA break repair", Cancer Letters (2016).
Paper Link
39. Singh N et al. "Insights into the mechanism of human papillomavirus E2-induced procaspase-8 activation and cell death", Scientific reports (2016).
Paper Link
38. Wu Y et al. " In-situ coupling between kinase activities and protein dynamics within single focal adhesions", Scientific reports (2016).
Paper Link
37. Gosnell M et al. "Quantitative non-invasive cell characterisation and discrimination based on multispectral autofluorescence features", Scientific Report (2016).
Paper Link
36. Singh N et al. "Molecular basis of death effector domain chain assembly and its role in caspase-8 activation", The Faseb Journal (2016).
Paper Link
35. Koçer SS et al. ""Shaping" of cell signaling via AKAP-tethered PDE4D: Probing with AKAR2-AKAP5 biosensor", Journal of molecular signaling (2012).
Paper Link
34. Gomez-Godinez V et al. "Laser-induced shockwave paired with FRET: A method to study cell signaling", Microscopy research and technique (2015).
Paper Link
33. Zhuo Y et al. "Subcellular and Dynamic Coordination between Src Activity and Cell Protrusion in Microenvironment", Scientific reports (2015).
Paper Link
32. Ouyang M et al. "Genetically Encoded Fluorescent Biosensors for Live-Cell Imaging of MT1-MMP Protease Activity", Fluorescent Protein-Based Biosensors. Humana Press (2014).
Paper Link
31. Zeng H-T et al. "Prematuration with cyclic adenosine monophosphate modulators alters cumulus cell and oocyte metabolism and enhances developmental competence of in vitro-matured mouse oocytes", Biology of reproduction (2014).
Paper Link
30. Tabdili H et al. "Cadherin point mutations alter cell sorting and modulate GTPase signaling", Journal of cell science (2012).
Paper Link
29. Ouyang M et al. "Simultaneous visualization of protumorigenic Src and MT1-MMP activities with fluorescence resonance energy transfer", Cancer research (2010).
Paper Link
27. Sutton-McDowall ML et al. "Metabolic differences in bovine cumulus-oocyte complexes matured in vitro in the presence or absence of follicle-stimulating hormone and bone morphogenetic protein 15", Biology of reproduction (2012).
Paper Link
26. Liao X et al. "Visualization of Src and FAK activity during the differentiation process from HMSCs to osteoblasts", PLoS ONE (2012).
Paper Link
25.Sudiman J et al. "Bone morphogenetic protein 15 in the pro-mature complex form enhances bovine oocyte developmental competence", PLoS ONE (2014).
Paper Link
24. Csordás G et al. "In vivo immunostaining of hemocyte compartments in Drosophila for live imaging", PLoS ONE (2014).
Paper Link
23. Xiang X et al. "A FRET-based biosensor for imaging SYK activities in living cells", Cellular and molecular bioengineering (2011).
Paper Link
22. Richani D et al. "Effect of epidermal growth factor-like peptides on the metabolism of in vitro-matured mouse oocytes and cumulus cells", Biology of reproduction (2014).
Paper Link
21. Lin L-J et al. "The antagonistic roles of PDGF and integrin αvβ3 in regulating ROS production at focal adhesions", Biomaterials (2013).
Paper Link
20. Poh Y-C et al. "The use of Optical Magnetic Twisting Cytometry and Flourescence Resonance Energy Transfer to quantify force-induced protein dissociation in the nucleus of a living cell", nature ProtocolExchange (2012).
Paper Link
19. Chung EY et al. "Activatable and Cell-Penetrable Multiplex FRET Nanosensor for Profiling MT1-MMP Activity in Single Cancer Cells", Nano letters (2015).
Paper Link
18. Bhave M et al. "Golgi enlargement in Arf-depleted yeast cells is due to altered dynamics of cisternal maturation", Journal of cell science (2014).
Paper Link
17. Seong J et al. "Detection of focal adhesion kinase activation at membrane microdomains by fluorescence resonance energy transfer", Nature communications (2011).
Paper Link
16. Lu S et al. "Quantitative FRET imaging to visualize the invasiveness of live breast cancer cells", PLoS ONE (2013).
Paper Link
15. Purdey MS et al. "Localised hydrogen peroxide sensing for reproductive health", SPIE Optics+ Optoelectronics. International Society for Optics and Photonics (2015).
Paper Link
14. Liao X et al. "The Effect of Differentiation Induction on FAK and Src Activity in Live HMSCs Visualized by FRET", PLoS ONE (2013).
Paper Link
13. Lu S et al. "Computational analysis of the spatiotemporal coordination of polarized PI3K and Rac1 activities in micro-patterned live cells", PLoS ONE (2011).
Paper Link
12. Kind KL et al. "Oxygen-regulated gene expression in murine cumulus cells", Reproduction, Fertility and Development (2015).
Paper Link
11. Lei L et al. "The role of mechanical tension on lipid raft dependent PDGF-induced TRPC6 activation", Biomaterials (2014).
Paper Link
10. Barry AK et al. "Local VE-cadherin mechanotransduction triggers long-ranged remodeling of endothelial monolayers", Journal of cell science (2015).
Paper Link
9. Sutton-McDowall ML et al. "Redox and anti-oxidant state within cattle oocytes following in vitro maturation with bone morphogenetic protein 15 and follicle stimulating hormone", Molecular reproduction and development (2015).
Paper Link
8. Ouyang M et al. "N-cadherin regulates spatially polarized signals through distinct p120ctn and β-catenin-dependent signalling pathways", Nature communications (2013).
Paper Link
7. Sun J et al. "Antagonism between binding site affinity and conformational dynamics tunes alternative cis-interactions within Shp2", Nature communications (2013).
Paper Link
6.Eichorst JP et al. "Red-shifted fluorescent proteins monitor enzymatic activity in live HT-1080 cells with fluorescence lifetime imaging microscopy (FLIM)", Journal of microscopy (2012).
Paper Link
5. Sun J et al. "Simplicity of Design Principles underlying Tunable cis-Interactions within Shp2 Revealed by FRET", (2013).
Paper Link
4. Lu S et al. "Decipher the dynamic coordination between enzymatic activity and structural modulation at focal adhesions in living cells", Scientific reports (2014).
Paper Link
3. Sun J, "The intramolecular domain interactions and phosphatase activation mechanisms of Shp2", Diss. University of Illinois, Urbana-Champaign (2011).
Paper Link
2. Sudiman J, "Optimisation of oocyte in vitro maturation using oocyte secreted factors", Diss. (2014).
Paper Link
1. Seong J, "Fluorescence resonance energy transfer-based subcellular visualization of FAK/Src activation by chemical and mechanical environment", Diss. University of Illinois, Urbana-Champaign (2013).
Paper Link
关键字： Cell E&G;Cell E&G代理;Cell E&G玻底培养皿;Cell E&G培养皿;
维百奥（北京）生物科技有限公司成立于2014年，经营范围包括: 技术服务、技术开发、技术咨询、技术交流、技术转让、技术推广;仪器仪表制造;仪器仪表销售;仪器仪表修理;化工产品生产(不含许可类化工产品);化工产品销售(不含许可类化工产品);专用化学产品制造(不含危险化学品);专用化学产品销售(不含危险化学品);计算机系统服务;数据处理和存储支持服务;软件开发;工程技术服务(规划管理、勘察、设计、监理除外);新材料技术推广服务;进出口代理;货物进出口;技术进出口。(除依法须经批准的项目外，凭营业执照依法自主开展经营活动)(不得从事国家和本市产业政策禁止和限制类项目的经营活动。)