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746223

Sigma-Aldrich

Maleimide-PEG2-succinimidyl ester

≥95%

Synonym(e):

3-[2-[2-[[3-(2,5-Dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]amino]ethoxy]ethoxy]propanoic acid 2,5-dioxo-1-pyrrolidinyl ester, Maleimide-PEG2-NHS

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About This Item

Empirische Formel (Hill-System):
C18H23N3O9
CAS-Nummer:
955094-26-5
Molekulargewicht:
425.39
MDL-Nummer:
MFCD11041137
UNSPSC-Code:
12352200
PubChem Substanz-ID:
329765750
NACRES:
NA.22

Qualitätsniveau

100

Assay

≥95%

Form

solid

Eignung der Reaktion

reaction type: Pegylations
reagent type: cross-linking reagent

mp (Schmelzpunkt)

92-94 °C

Funktionelle Gruppe

NHS ester
maleimide

Lagertemp.

−20°C

SMILES String

O=C(N1CCC(NCCOCCOCCC(ON(C(CC2)=O)C2=O)=O)=O)C=CC1=O

InChI

1S/C18H23N3O9/c22-13(5-8-20-14(23)1-2-15(20)24)19-7-10-29-12-11-28-9-6-18(27)30-21-16(25)3-4-17(21)26/h1-2H,3-12H2,(H,19,22)

InChIKey

TZPDZOJURBVWHS-UHFFFAOYSA-N

Anwendung

Heterobifunctional crosslinker with short ethylene oxide spacer for linking amine- to sulfhydryl-containing compounds or biomolecules. Maleimide functional group will react with sulfhydryls and the succinimidyl ester group will react with amines. Spacer length is 17.6 angstroms.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCS3428
MKCW3843
MKCT9228
MKCQ4466
MKCP2457

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Sabrina Simoncelli et al.
Cell reports, 33(12), 108523-108523 (2020-12-29)
Elucidating the mechanisms that controlled T cell activation requires visualization of the spatial organization of multiple proteins on the submicron scale. Here, we use stoichiometrically accurate, multiplexed, single-molecule super-resolution microscopy (DNA-PAINT) to image the nanoscale spatial architecture of the primary inhibitor
Nirakar Basnet et al.
Nature cell biology, 20(10), 1172-1180 (2018-09-27)
Microtubules are central elements of the eukaryotic cytoskeleton that often function as part of branched networks. Current models for branching include nucleation of new microtubules from severed microtubule seeds or from γ-tubulin recruited to the side of a pre-existing microtubule.
Sinem K Saka et al.
Nature biotechnology, 37(9), 1080-1090 (2019-08-21)
Spatial mapping of proteins in tissues is hindered by limitations in multiplexing, sensitivity and throughput. Here we report immunostaining with signal amplification by exchange reaction (Immuno-SABER), which achieves highly multiplexed signal amplification via DNA-barcoded antibodies and orthogonal DNA concatemers generated
Florian Schueder et al.
Nature communications, 8(1), 2090-2090 (2017-12-14)
Single-molecule localization microscopy (SMLM) can visualize biological targets on the nanoscale, but complex hardware is required to perform SMLM in thick samples. Here, we combine 3D DNA points accumulation for imaging in nanoscale topography (DNA-PAINT) with spinning disk confocal (SDC)
Thomas Schlichthaerle et al.
Chembiochem : a European journal of chemical biology, 20(8), 1032-1038 (2018-12-28)
Current optical super-resolution implementations are capable of resolving features spaced just a few nanometers apart. However, translating this spatial resolution to cellular targets is limited by the large size of traditionally employed primary and secondary antibody reagents. Recent advancements in

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