跳转至内容
Merck

72709

Sigma-Aldrich

Atto 488叠氮化物

BioReagent, suitable for fluorescence, ≥90% (HPLC)

登录查看公司和协议定价


About This Item

分類程式碼代碼:
12352125
NACRES:
NA.32

產品線

BioReagent

化驗

≥90% (HPLC)

形狀

solid

分子量

Mw 903 g/mol

製造商/商標名

ATTO-TEC GmbH

&lambda ;

in methanol: water (1:1) (with 0.1% perchloric acid)

紫外吸收

λ: 501-507 nm Amax

適合性

suitable for fluorescence

儲存溫度

−20°C

相关类别

一般說明

Atto 488是一种出色的荧光标记,具有高分子吸收(90.000)和量子产率(0.80)以及足够的斯托克斯′位移。它经过优化,可以用氩激光激发,并具有高光稳定性。
叠氮化物修饰适用于与炔烃基团的反应(Huisgen反应- “点击化学”)。

法律資訊

本品仅供研究使用。如果打算商业化,请联系知识产权持有者(德国ATTO-TEC GmbH公司)申请许可。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Monitoring single membrane protein dynamics in a liposome manipulated in solution by the ABELtrap.
Rendler, T., et al.
arXiv, 1102-1102 (2011)
Analysis of fluorescent nanostructures in biological systems by means of spectral position determination microscopy (SPDM).
Muller, P., et al. et al.
Current Microscopy Contributions to Advances in Science and Technology, 1, 3-12 (2012)
E Pourkarimi et al.
Cell death and differentiation, 19(3), 406-415 (2011-09-03)
In C. elegans, the BH3-only domain protein EGL-1, the Apaf-1 homolog CED-4 and the CED-3 caspase are required for apoptosis induction, whereas the Bcl-2 homolog CED-9 prevents apoptosis. Mammalian B-cell lymphoma 2 (Bcl-2) inhibits apoptosis by preventing the release of
Jeanne C Stachowiak et al.
Nature cell biology, 14(9), 944-949 (2012-08-21)
Curved membranes are an essential feature of dynamic cellular structures, including endocytic pits, filopodia protrusions and most organelles. It has been proposed that specialized proteins induce curvature by binding to membranes through two primary mechanisms: membrane scaffolding by curved proteins
Markus Hirsch et al.
Biological chemistry, 393(1-2), 23-35 (2012-05-26)
Investigations into the fate of small interfering RNA (siRNA) after transfection may unravel new ways to improve RNA interference (RNAi) efficiency. Because intracellular degradation of RNA may prevent reliable observation of fluorescence-labeled siRNA, new tools for fluorescence microscopy are warranted

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门