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1,1,2,2-tetrakis[4-(8-bromooctyloxy)phenyl]-ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1219133-99-9

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1219133-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219133-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,1,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1219133-99:
(9*1)+(8*2)+(7*1)+(6*9)+(5*1)+(4*3)+(3*3)+(2*9)+(1*9)=139
139 % 10 = 9
So 1219133-99-9 is a valid CAS Registry Number.

1219133-99-9Downstream Products

1219133-99-9Relevant academic research and scientific papers

Water-soluble AIE luminogens for monitoring and retardation of fibrillation of amyloid proteins

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Page/Page column 62, (2016/04/20)

Compounds that exhibit aggregation induced emission (AIE), and more particularly to water-soluble conjugated polyene compounds that exhibit aggregation induced emission. The conjugated polyene compounds can be used as bioprobes for DNA detection, G-quadru

Fluorescent bioprobes: Structural matching in the docking processes of aggregation-induced emission fluorogens on DNA surfaces

Hong, Yuning,Xiong, Hao,Lam, Jacky Wing Yip,Haeussler, Matthias,Liu, Jianzhao,Yu, Yong,Zhong, Yongchun,Sung, Herman H.Y.,Williams, Ian D.,Wong, Kam Sing,Tang, Ben Zhong

supporting information; experimental part, p. 1232 - 1245 (2010/06/14)

Whereas most conventional DNA probes are flat disklike aromatic molecules, we explored the possibility of developing quadruplex sensors with nonplanar conformations, in particular, the propeller-shaped tetraphenylethene (TPE) salts with aggregation-induced emission (AIE) characteristics. 1,1,2,2-Tetrakis[4-(2- triethylammonioethoxy)-phenyljethene tetrabromide (TPE-1) was found to show a specific affinity to a particular quadruplex structure formed by a human telomeric DNA strand in the presence of K+ ions, as indicated by the enhanced and bathochromically shifted emission of the AIE fluorogen. Steady-state and time-resolved spectral analyses revealed that the specific binding stems from a structural matching between the AIE fluorogen and the DNA strand in the folding process. Computational modeling suggests that the AIE molecule docks on the grooves of the quadruplex surface with the aid of electrostatic attraction. The binding preference of TPE-1 enables it to serve as a bioprobe for direct monitoring of cation-driven conformational transitions between the quadruplexes of various conformations, a job unachievable by the traditional G-quadruplex biosensors. Methyl thiazolyl tetrazolium (MTT) assays reveal that TPE-1 is cytocompatible, posing no toxicity to living cells.

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