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714960-84-6

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714960-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714960-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,9,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 714960-84:
(8*7)+(7*1)+(6*4)+(5*9)+(4*6)+(3*0)+(2*8)+(1*4)=176
176 % 10 = 6
So 714960-84-6 is a valid CAS Registry Number.

714960-84-6Upstream product

714960-84-6Downstream Products

714960-84-6Relevant academic research and scientific papers

An easily regenerable enzyme reactor prepared from polymerized high internal phase emulsions

Ruan, Guihua,Wu, Zhenwei,Huang, Yipeng,Wei, Meiping,Su, Rihui,Du, Fuyou

, p. 54 - 60 (2016/04/20)

A large-scale high-efficient enzyme reactor based on polymerized high internal phase emulsion monolith (polyHIPE) was prepared. First, a porous cross-linked polyHIPE monolith was prepared by in-situ thermal polymerization of a high internal phase emulsion containing styrene, divinylbenzene and polyglutaraldehyde. The enzyme of TPCK-Trypsin was then immobilized on the monolithic polyHIPE. The performance of the resultant enzyme reactor was assessed according to the conversion ability of Nα-benzoyl-l-arginine ethyl ester to Nα-benzoyl-l-arginine, and the protein digestibility of bovine serum albumin (BSA) and cytochrome (Cyt-C). The results showed that the prepared enzyme reactor exhibited high enzyme immobilization efficiency and fast and easy-control protein digestibility. BSA and Cyt-C could be digested in 10 min with sequence coverage of 59% and 78%, respectively. The peptides and residual protein could be easily rinsed out from reactor and the reactor could be regenerated easily with 4 M HCl without any structure destruction. Properties of multiple interconnected chambers with good permeability, fast digestion facility and easily reproducibility indicated that the polyHIPE enzyme reactor was a good selector potentially applied in proteomics and catalysis areas.

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