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BrainPhys™ 神经元培养基N2-A和SM1试剂盒

用于在BrainPhys™神经元培养基中无血清培养ES/iPS细胞来源的神经元

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产品号 #（选择产品）

产品号 #05793_C

用于在BrainPhys™神经元培养基中无血清培养ES/iPS细胞来源的神经元

产品优势

更好地模拟大脑内的细胞外环境
增强神经元功能，获得更高比例的突触活性神经元
无需更换培养基并避免因此造成的细胞应激，即可进行功能性检测
支持由ES/iPS细胞及CNS来源的神经元的长期培养
严格的原材料筛选和质量控制可确保将批次间的差异性降至最低

产品组分包括

BrainPhys™神经元培养基，500 mL（产品号 #05790）
NeuroCult™ SM1神经元添加物，10 mL（产品号 #05711）

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What Our Scientist Says

I want to help neuroscientists like you create more physiological culture conditions, for more active and healthy neuronal cultures.

Carmen MakScientist

总览

实验数据

产品说明书及文档

应用领域

总览

使用经过优化、旨在促进而非抑制神经元活性的完整培养基，对来源于人胚胎干细胞（ES）或诱导多能干细胞（iPS）的神经元进行培养、分化和成熟。

为方便使用，BrainPhys™神经元培养基N2-A和SM1试剂盒包含BrainPhys™神经元培养基（基础培养基）和用于培养人ES/iPS来源神经元祖细胞的添加物。基于Bardy和Gage的配方（Bardy et al. PNAS, 2015），无血清的BrainPhys™神经元培养基模拟了中枢神经系统（CNS）的细胞外环境，可获得更高比例的突触活性神经元。基于Brewer的B27配方（Brewer et al. J Neurosci Res., 1993）的NeuroCult™ SM1神经元添加物可在短期和长期无血清培养中维持细胞健康，并促进神经突起的生长和分支，而N2-A添加物则支持ES/iPS来源的细胞向神经元亚型的体外分化。若需进行依赖生长因子的谱系特异性分化，请参阅BrainPhys™ hPSC神经元试剂盒，该试剂盒还包含BDNF和GDNF。

为避免在更换培养基时对细胞造成应激，在进行诸如微电极阵列记录或活细胞荧光成像等功能性检测时，也可使用 BrainPhys™ 培养基。

查看我们的其他资源，了解更多关于BrainPhys™system的信息。

为避免在更换培养基时对细胞造成应激，在进行诸如微电极阵列记录或活细胞荧光成像等功能性检测时，也可使用 BrainPhys™ 培养基。

查看我们的其他资源，了解更多关于BrainPhys™system的信息。

为避免在更换培养基时对细胞造成应激，在进行诸如微电极阵列记录或活细胞荧光成像等功能性检测时，也可使用 BrainPhys™ 培养基。

查看我们的其他资源，了解更多关于BrainPhys™system的信息。

为避免在更换培养基时对细胞造成应激，在进行诸如微电极阵列记录或活细胞荧光成像等功能性检测时，也可使用 BrainPhys™ 培养基。

查看我们的其他资源，了解更多关于BrainPhys™system的信息。

亚型
基础培养基，专用培养基

细胞类型
神经细胞，PSC衍生，神经元，多能干细胞

种属
人

应用
细胞培养，分化，培养

品牌
BrainPhys

研究领域
疾病建模，药物发现和毒理检测，神经科学，干细胞生物学

制剂类别
无血清

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实验数据

Table 1. Properties of Culture Media (C Bardy et al. Proc Natl Acad Sci USA, 2015)

Check-mark denotes physiological conditions and supported activities according to C Bardy et al. Proc Natl Acad Sci USA, 2015.

Rodent Neurons Matured in BrainPhys™ Neuronal Medium

Figure 1. Protocol for Culturing hPSCs with the SM1 Culture System

hPSCs were maintained in mTeSR™1 medium and then differentiated using the STEMdiff™ SMADi Neural Induction Kit. Following plating on PLO/laminin, half-medium changes were performed to transition to BrainPhys™ Neuronal Medium for maturation and long-term culture.

hPSC-Derived Neurons Generated in BrainPhys™ Neuronal Medium and NeuroCult™ SM1 and N2 Supplements are Healthy and Morphologically Normal

Figure 2. hPSC-Derived Neurons Generated in BrainPhys™ Neuronal Medium and NeuroCult™ SM1 and N2 Supplements are Healthy and Morphologically Normal

NPCs were generated from H9 cells using STEMdiff™ Neural Induction Medium in an embryoid body-based protocol. Next, NPCs were cultured for 44 DIV in (A) BrainPhys™ Neuronal Medium, supplemented with 2% NeuroCult™ SM1 Supplement, 1% N2 Supplement-A, 20 ng/mL GDNF, 20 ng/mL BDNF, 1 mM db-cAMP and 200 nM ascorbic acid to initiate neuronal differentiation, or (B) DMEM/F12 under the same supplementation conditions. Neuronal cultures differentiated from NPCs in BrainPhys™ Neuronal Medium display extensive neurite outgrowth and reduced cellular debris compared to cultures differentiated in DMEM/F12. Scale bar= 100 µm.

产品说明书及文档

请在《产品说明书》中查找相关支持信息和使用说明，或浏览下方更多实验方案。

Document Type

Product Name

Catalog #

Lot #

Language

Document Type

Product Information Sheet

Product Name

BrainPhys™ Neuronal Medium N2-A & SM1 Kit

Catalog #

05793

Lot #

All

Language

English

Document Type

Safety Data Sheet 1

Product Name

BrainPhys™ Neuronal Medium N2-A & SM1 Kit

Catalog #

05793

Lot #

All

Language

English

Document Type

Safety Data Sheet 2

Product Name

BrainPhys™ Neuronal Medium N2-A & SM1 Kit

Catalog #

05793

Lot #

All

Language

English

Document Type

Safety Data Sheet 3

Product Name

BrainPhys™ Neuronal Medium N2-A & SM1 Kit

Catalog #

05793

Lot #

All

Language

English

应用领域

本产品专为以下研究领域设计，适用于工作流程中的高亮阶段。探索这些工作流程，了解更多我们为各研究领域提供的其他配套产品。

Research Area

Workflow Stages

Workflow Stages for Human Pluripotent Stem Cell Research

Reprogramming

Maintenance

Differentiation

Workflow Stages for hPSC-Derived Neural Cell Research

Cell Sourcing

Neural Induction

Expansion

Differentiation and Maturation

Characterization

Workflow Stages for Neuronal Research

Tissue Dissociation

Cell Culture

Characterization

相关材料与文献

Modelling Lyssavirus Infections in Human Stem Cell-Derived Neural Cultures. V. Sundaramoorthy et al. Viruses 2020 mar

Abstract

Rabies is a zoonotic neurological infection caused by lyssavirus that continues to result in devastating loss of human life. Many aspects of rabies pathogenesis in human neurons are not well understood. Lack of appropriate ex-vivo models for studying rabies infection in human neurons has contributed to this knowledge gap. In this study, we utilize advances in stem cell technology to characterize rabies infection in human stem cell-derived neurons. We show key cellular features of rabies infection in our human neural cultures, including upregulation of inflammatory chemokines, lack of neuronal apoptosis, and axonal transmission of viruses in neuronal networks. In addition, we highlight specific differences in cellular pathogenesis between laboratory-adapted and field strain lyssavirus. This study therefore defines the first stem cell-derived ex-vivo model system to study rabies pathogenesis in human neurons. This new model system demonstrates the potential for enabling an increased understanding of molecular mechanisms in human rabies, which could lead to improved control methods.

View publication

One-Stop Microfluidic Assembly of Human Brain Organoids To Model Prenatal Cannabis Exposure. Z. Ao et al. Analytical chemistry 2020

Abstract

Prenatal cannabis exposure (PCE) influences human brain development, but it is challenging to model PCE using animals and current cell culture techniques. Here, we developed a one-stop microfluidic platform to assemble and culture human cerebral organoids from human embryonic stem cells (hESC) to investigate the effect of PCE on early human brain development. By incorporating perfusable culture chambers, air-liquid interface, and one-stop protocol, this microfluidic platform can simplify the fabrication procedure and produce a large number of organoids (169 organoids per 3.5 cm × 3.5 cm device area) without fusion, as compared with conventional fabrication methods. These one-stop microfluidic assembled cerebral organoids not only recapitulate early human brain structure, biology, and electrophysiology but also have minimal size variation and hypoxia. Under on-chip exposure to the psychoactive cannabinoid, $\Delta$-9-tetrahydrocannabinol (THC), cerebral organoids exhibited reduced neuronal maturation, downregulation of cannabinoid receptor type 1 (CB1) receptors, and impaired neurite outgrowth. Moreover, transient on-chip THC treatment also decreased spontaneous firing in these organoids. This one-stop microfluidic technique enables a simple, scalable, and repeatable organoid culture method that can be used not only for human brain organoids but also for many other human organoids including liver, kidney, retina, and tumor organoids. This technology could be widely used in modeling brain and other organ development, developmental disorders, developmental pharmacology and toxicology, and drug screening.

View publication

Maturation of Human Pluripotent Stem Cell-Derived Cerebellar Neurons in the Absence of Co-culture. T. P. Silva et al. Frontiers in bioengineering and biotechnology 2020

Abstract

The cerebellum plays a critical role in all vertebrates, and many neurological disorders are associated with cerebellum dysfunction. A major limitation in cerebellar research has been the lack of adequate disease models. As an alternative to animal models, cerebellar neurons differentiated from pluripotent stem cells have been used. However, previous studies only produced limited amounts of Purkinje cells. Moreover, in vitro generation of Purkinje cells required co-culture systems, which may introduce unknown components to the system. Here we describe a novel differentiation strategy that uses defined medium to generate Purkinje cells, granule cells, interneurons, and deep cerebellar nuclei projection neurons, that self-formed and differentiated into electrically active cells. Using a defined basal medium optimized for neuronal cell culture, we successfully promoted the differentiation of cerebellar precursors without the need for co-culturing. We anticipate that our findings may help developing better models for the study of cerebellar dysfunctions, while providing an advance toward the development of autologous replacement strategies for treating cerebellar degenerative diseases.

View publication

View All Publications