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Key Documents

08-110

Sigma-Aldrich

ECL细胞附着基质

别名:

ECL Matrix

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About This Item

分類程式碼代碼:
12352202
eCl@ss:
32160405
NACRES:
NA.75

生物源

mouse

品質等級

形狀

liquid

製造商/商標名

Upstate®

技術

cell culture | mammalian: suitable

輸入

sample type neural stem cell(s)
sample type mesenchymal stem cell(s)
sample type induced pluripotent stem cell(s)
sample type hematopoietic stem cell(s)
sample type: human embryonic stem cell(s)
sample type epithelial cells
sample type pancreatic stem cell(s)

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

来自Engelbreth-Holm-Swarm(EHS)小鼠肿瘤的ECL细胞附着基质。

應用

细胞培养附着因子

品質

使用PC12大鼠嗜铬细胞瘤细胞在神经突生长试验中进行常规评估。

外觀

5 mg溶于5 ml 0.05 M Tris-HCl(pH 7.4),0.15 M NaCl。 使用γ球蛋白作为标准品,通过Bradford染料结合测定法测定蛋白质。 冷冻溶液。

儲存和穩定性

自收到之日起在-20°C可稳定保存1年。 避免反复冻融。

法律資訊

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Basement membrane complexes with biological activity.
Kleinman, H K, et al.
Biochemistry, 25, 312-318 (1986)
Alteration of Ca2+ dependence of neurotransmitter release by disruption of Ca2+ channel/syntaxin interaction
Rettig, J., et al
The Journal of Neuroscience, 17, 6647-6656 (1997)
Extracellular matrix regulates Sertoli cell differentiation, testicular cord formation, and germ cell development in vitro.
Hadley, M A, et al.
The Journal of cell biology, 101, 1511-1522 (1985)
F B Gertler et al.
Cell, 87(2), 227-239 (1996-10-18)
Drosophila Enabled is required for proper formation of axonal structures and is genetically implicated in signaling pathways mediated by Drosophila AbI. We have identified two murine proteins, Mena and Evl, that are highly related to Enabled as well as VASP
B B Friday et al.
The Journal of cell biology, 149(3), 657-666 (2000-05-03)
Differentiation of skeletal muscle myoblasts follows an ordered sequence of events: commitment, cell cycle withdrawal, phenotypic differentiation, and finally cell fusion to form multinucleated myotubes. The molecular signaling pathways that regulate the progression are not well understood. Here we investigate

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