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Merck

QBD10247

Sigma-Aldrich

Thiol-dPEG®4-acid

>95% (HPLC)

Synonym(e):

Carboxy-PEG4-thiol, HS-PEG4-COOH, Thiol-PEG-acid, Thiol-PEG4-COOH, Thiol-PEG4-acid

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About This Item

Empirische Formel (Hill-System):
C11H22O6S
Molekulargewicht:
282.35
MDL-Nummer:
UNSPSC-Code:
12352106
NACRES:
NA.22

Assay

>95% (HPLC)

Form

solid or viscous liquid

Eignung der Reaktion

reaction type: Pegylations

Polymerarchitektur

shape: linear
functionality: heterobifunctional

Versandbedingung

ambient

Lagertemp.

−20°C

Leistungsmerkmale und Vorteile

Thiol-dPEG4-acid is a sulfhydryl-containing, crosslinking PEGylation reagent that has a cross-bridge of monodisperse polyethylene glycol. The single molecular weight, discrete-length PEG (dPEG) chain is 16 atoms (18.3 Å) long. The sulfhydryl end of the crosslinker reacts with gold (forming dative bonds) and with thiol-reactive functional groups such as maleimide, bromoacetyl, SPDP, and thiol. The carboxylic acid end of the molecule couples to free amines using EDC or any suitable carbodiimide. An acylating agent such as N-hydroxysuccinimide (NHS) or 2,3,5,6-tetrafluorophenol (TFP) can enhance coupling efficiency. The carboxylate must react after the sulfhydryl conjugation.

Rechtliche Hinweise

Products Protected under U.S. Patent #s 7,888,536 & 8,637,711 and European Patent #s 1,594,440 & 2,750,681
dPEG is a registered trademark of Quanta BioDesign

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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BioMed research international, 2017, 5041683-5041683 (2017-05-02)
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Daichi Okuno et al.
Nanoscale, 10(8), 4036-4040 (2018-02-13)
The artificial bilayer single channel recording technique is commonly used to observe the detailed physiological properties of various ion channel proteins. It permits easy control of the solution and membrane lipid composition, and is also compatible with pharmacological screening devices.
Carrie A Simpson et al.
ACS nano, 5(5), 3577-3584 (2011-04-09)
Monolayer-protected gold nanoparticles have great potential as novel building blocks for the design of new drugs and therapeutics based on the easy ability to multifunctionalize them for biological targeting and drug activity. In order to create nanoparticles that are biocompatible

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