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Merck
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Key Documents

181978

Sigma-Aldrich

Poly(éthylèneimine) solution

average Mn ~60,000 by GPC, average Mw ~750,000 by LS, 50 wt. % in H2O

Synonyme(s) :

PEI, Polymère d'éthylèneimine solution

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About This Item

Numéro CAS:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pression de vapeur

9 mmHg ( 20 °C)

Poids mol.

average Mn ~60,000 by GPC
average Mw ~750,000 by LS

Concentration

50 wt. % in H2O

InChI

1S/C2H5N/c1-2-3-1/h3H,1-2H2

Clé InChI

NOWKCMXCCJGMRR-UHFFFAOYSA-N

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Application

Detergents, adhesives, water treatment, printing inks, dyes, cosmetics, and paper industry, adhesion promoter, lamination primer, fixative agent, flocculant, cationic dispersant, stability enhancer, surface activator, chelating agent, scavenger for aldehydes and oxides.
Protein precipitant.

Forme physique

Branched polymer

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

J Y Zhao et al.
Journal of biotechnology, 14(3-4), 273-283 (1990-06-01)
Protein recovery from industrial microbial processes can be very expensive, often exceeding the cost of protein production. We have genetically engineered 3 beta-galactosidase (beta-gal) fusion proteins containing poly-aspartic acid tails to test the effect of the tails on recovery by
Jason C Casler et al.
Molecular biology of the cell, 31(26), 2892-2903 (2020-10-29)
Membrane traffic can be studied by imaging a cargo protein as it transits the secretory pathway. The best tools for this purpose initially block export of the secretory cargo from the endoplasmic reticulum (ER) and then release the block to
Andrew Jajack et al.
PloS one, 14(1), e0210286-e0210286 (2019-01-17)
Insurmountable detection challenges will impede the development of many of the next-generation of lab-on-a-chip devices (e.g., point-of-care and real-time health monitors). Here we present the first membrane-based, microfluidic sample preconcentration method that is continuous, quantifiable, simple, and capable of working
Xinyue Yuan et al.
Nature communications, 11(1), 4854-4854 (2020-09-27)
Chronic imaging of neuronal networks in vitro has provided fundamental insights into mechanisms underlying neuronal function. Current labeling and optical imaging methods, however, cannot be used for continuous and long-term recordings of the dynamics and evolution of neuronal networks, as
Kevin Bellande et al.
Plant physiology and biochemistry : PPB, 157, 441-452 (2020-11-20)
An efficient purification of recombinant proteins often requires a high ratio of recombinant to host proteins. In plants, Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) is the most abundant leaf protein, thus strongly impacting purification yield. Here, we describe a simple and robust purification

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Gene therapy has become one of the most discussed techniques in biomedical research in recent years.

Professor Yoshiki Katayama (Kyushu University, Japan) discusses recent advances in drug delivery systems and strategies that exploit the EPR effect, with a special focus on stimuli-responsive systems based on novel materials.

We present an article that discusses two applications in particular; first, using these layers as polyelectrolyte membranes to control permeability.

Microfluidic assembly improves polyamine nanoencapsulation of nucleic acids, overcoming challenges like polydispersity and poor reproducibility.

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