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Merck

181978

Sigma-Aldrich

Polyethylenimin -Lösung

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

Synonym(e):

Ethylenimin-Polymer -Lösung, PEI

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About This Item

CAS-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23

Dampfdruck

9 mmHg ( 20 °C)

Mol-Gew.

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

Konzentration

50 wt. % in H2O

InChI

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

InChIKey

NOWKCMXCCJGMRR-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

Detergenzien, Klebstoffe, Wasseraufbereitung, Druckfarben, Farbstoffe, Kosmetika und Papierindustrie, Haftvermittler, Beschichtungsprimer, Fixiermittel, Flockungsmittel, kationische Dispergierungsmittel, Stabilisatoren, Oberflächenaktivatoren, Chelatbildner, Radikalfänger für Aldehyde und Oxide.
Protein-Fällungsmittel.

Physikalische Form

Verzweigtes Polymer

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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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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