N-2 Supplement (100X)
N-2 Supplement (100X)
Gibco™

N-2 Supplement (100X)

N-2補完は、Bottenstein N-1の組成に基づく、化学的に定義された無血清の補完です。末梢神経系と中枢神経系の両方からの初代培養における神経芽腫の成長と発現、および有糸分裂後の神経細胞に推奨されます。N-2補完は100倍の濃縮液として提供され、bFGFやEGFなどの増殖因子を添加したNeurobasal培地と併用することを目的としています。DMEMとも併用できます。N-2補完を使用して確立されたプロトコルについては詳細を見る
製品番号(カタログ番号)数量
175020485 mL
1750200150 mL
製品番号(カタログ番号) 17502048
価格(JPY)
30,600
Each
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数量:
5 mL
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N-2補完は、Bottenstein N-1の組成に基づく、化学的に定義された無血清の補完です。末梢神経系と中枢神経系の両方からの初代培養における神経芽腫の成長と発現、および有糸分裂後の神経細胞に推奨されます。N-2補完は100倍の濃縮液として提供され、bFGFやEGFなどの増殖因子を添加したNeurobasal培地と併用することを目的としています。DMEMとも併用できます。

N-2補完を使用して確立されたプロトコルについては、当社のGibco神経生物学プロトコルハンドブックをご覧ください。

Gibco神経生物学製品を使用した出版物については、CellCiteをご覧ください。

研究用にのみ使用できます。診断用には使用いただけません。
仕様
細胞タイプNeural Cells
濃度100 X
培養タイプMammalian Cell Culture
数量5 mL
血清レベルSerum-Free
品質保持期間18 Months
出荷条件Dry Ice
試験済みEndotoxin, Performance, Sterility
分類Serum-free
形状Liquid
製品タイプCell Culture Supplement
無菌性Sterile
pH6 to 8
Unit SizeEach
組成および保存条件
Store in freezer (-5 to -20°C) and protect from light.

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ドキュメントおよびダウンロード

証明書

ロット番号Certificate TypeDateCatalog Number(s)
2868587Certificate of Analysis2025年6月01日17502001, 17502048
3011306Certificate of Analysis2025年5月31日17502001, 17502048
3062758Certificate of Analysis2025年5月16日17502001, 17502048
2868579Certificate of Analysis2025年4月20日17502001, 17502048
2868577Certificate of Analysis2025年4月04日17502001, 17502048
5件の結果が表示されました。 上記から特定の証明書を検索します

Safety Data Sheets

よくあるご質問(FAQ)

Neurobasal and Neurobasal-A media (for postnatal and adult neurons) allow for long-term maintenance of neuronal cells without the need for an astrocyte feeder layer. These media should be supplemented with either serum or a serum-free supplement, plus 0.5mM L-glutamine. B-27 supplement is a serum-free supplement that comes as a 50X concentrate in a 10ml volume. This is enough supplement for 500ml of media. Fetal, postnatal, and adult neural cultures can be grown in the appropriate Neurobasal medium supplemented with B-27 supplement .

We also have two other supplements. One is called G-5 and is for growth and expression of glial cells (normal and tumor) of astrocytic phenotype. This comes in a 1ml size, at a 100X concentration. The other supplement is called N-2 and is for growth and expression of post-mitotic neurons and tumor cells of neuronal phenotype. This comes in a 5ml size, at a 100X concentration.

For more information on Neurobasal media, search "Neurobasal" from our website home page.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Both N-2 Supplement formulations can be used in the culture of neurons, but the concentrations of components in the formula for the Global Stem N-2 Supplement are higher than the Gibco N-2 Supplement.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

The N-2 Supplement (100X) solution can be filtered. We do not recommend filtering the medium once N-2 has been added at a final concentration of 1X.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

The shelf life for N-2 Supplement (100X) is 18 months from the date of manufacture when stored at the recommended storage condition of -5 to -20 degrees C, protected from light. The expiration date should be listed on the product label as well as on the COA for the lot of the supplement.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

As a general guideline, we recommend using Gibco B-27 Plus Supplement to culture neural stem cells, hippocampal, and other CNS neurons.

- For neuroblastomas, or post-mitotic neurons from both PNS and CNS, Gibco N-2 Supplement can be used.
- For primary glial cells (astrocytes) or tumor cell lines of astrocytic phenotype (astrocytes and gliomas), or oligodendrocytes, Gibco G-5 Supplement can be used.

引用および参考文献 (5)

引用および参考文献
Abstract
A comprehensive protocol for efficient differentiation of human NPCs into electrically competent neurons.
Authors:Romito E,Battistella I,Plakhova V,Paplekaj A,Forastieri C,Toffolo E,Musio C,Conti L,Battaglioli E,Rusconi F
Journal:Journal of neuroscience methods
PubMed ID:39053772
In vitro generation of human pluripotent stem cell derived lung organoids.
Authors:Dye BR, Hill DR, Ferguson MA, Tsai YH, Nagy MS, Dyal R, Wells JM, Mayhew CN, Nattiv R, Klein OD, White ES, Deutsch GH, Spence JR
Journal:
PubMed ID:25803487
'Recent breakthroughs in 3-dimensional (3D) organoid cultures for many organ systems have led to new physiologically complex in vitro models to study human development and disease. Here, we report the step-wise differentiation of human pluripotent stem cells (hPSCs) (embryonic and induced) into lung organoids. By manipulating developmental signaling pathways hPSCs ... More
Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro.
Authors:Spence JR, Mayhew CN, Rankin SA, Kuhar MF, Vallance JE, Tolle K, Hoskins EE, Kalinichenko VV, Wells SI, Zorn AM, Shroyer NF, Wells JM
Journal:Nature
PubMed ID:21151107
Studies in embryonic development have guided successful efforts to direct the differentiation of human embryonic and induced pluripotent stem cells (PSCs) into specific organ cell types in vitro. For example, human PSCs have been differentiated into monolayer cultures of liver hepatocytes and pancreatic endocrine cells that have therapeutic efficacy in ... More
Recapitulation of SARS-CoV-2 infection and cholangiocyte damage with human liver ductal organoids.
Authors:Zhao B, Ni C, Gao R, Wang Y, Yang L, Wei J, Lv T, Liang J, Zhang Q, Xu W, Xie Y, Wang X, Yuan Z, Liang J, Zhang R, Lin X
Journal:Protein Cell
PubMed ID:32303993
Viral Delivery of GDNF Promotes Functional Integration of Human Stem Cell Grafts in Parkinson's Disease.
Authors:Gantner CW, de Luzy IR, Kauhausen JA, Moriarty N, Niclis JC, Bye CR, Penna V, Hunt CPJ, Ermine CM, Pouton CW, Kirik D, Thompson LH, Parish CL
Journal:Cell Stem Cell
PubMed ID:32059808
Dopaminergic neurons (DAns), generated from human pluripotent stem cells (hPSCs), are capable of functionally integrating following transplantation and have recently advanced to clinical trials for Parkinson's disease (PD). However, pre-clinical studies have highlighted the low proportion of DAns within hPSC-derived grafts and their inferior plasticity compared to fetal tissue. Here, ... More
5 total citations

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