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Key Documents

Safety Information

44613

Sigma-Aldrich

Durcupan ACM

single component C, accelerator 960 (DY 060)

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10 G
CN¥2,079.15
50 G
CN¥8,202.21
250 G
CN¥27,811.75

CN¥2,079.15


Available to ship onApril 27, 2025Details


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10 G
CN¥2,079.15
50 G
CN¥8,202.21
250 G
CN¥27,811.75

About This Item

MDL number:
UNSPSC Code:
12352106
NACRES:
NA.25

CN¥2,079.15


Available to ship onApril 27, 2025Details


Request a Bulk Order

Quality Level

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1 of 4

This Item
748847488551832
assay

≥99.0% (T)

assay

≥99.0% (T)

assay

≥97.0% (T)

assay

≥99.0% (T)

form

sheet

form

sheet

form

sheet

form

solid

suitability

corresponds to standard for RP gradient test, corresponds to standard for filter test

suitability

-

suitability

-

suitability

corresponds to standard for RP gradient test, corresponds to standard for filter test

technique(s)

ion pair chromatography: suitable

technique(s)

ion pair chromatography: suitable

technique(s)

-

technique(s)

ion pair chromatography: suitable

mol wt

234.29 g/mol

mol wt

234.29 g/mol

mol wt

-

mol wt

220.26 g/mol

mp

≥300 °C (lit.)

mp

≥300 °C (lit.)

mp

≥300 °C (lit.)

mp

-

Application

Embedding material for electron microscopy on the basis of Araldite®.

Legal Information

Araldite is a registered trademark of Huntsman Advanced Materials Inc.
Durcupan is a trademark of Sigma-Aldrich Chemie GmbH

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Product No.
Description
Pricing

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

监管及禁止进口产品

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    Tin Ki Tsang et al.
    eLife, 7 (2018-05-12)
    Electron microscopy (EM) offers unparalleled power to study cell substructures at the nanoscale. Cryofixation by high-pressure freezing offers optimal morphological preservation, as it captures cellular structures instantaneously in their near-native state. However, the applicability of cryofixation is limited by its
    Keun-Young Kim et al.
    Cell reports, 29(3), 628-644 (2019-10-17)
    The form and synaptic fine structure of melanopsin-expressing retinal ganglion cells, also called intrinsically photosensitive retinal ganglion cells (ipRGCs), were determined using a new membrane-targeted version of a genetic probe for correlated light and electron microscopy (CLEM). ipRGCs project to
    David E Gordon et al.
    Molecular cell, 78(2), 197-209 (2020-02-23)
    We have developed a platform for quantitative genetic interaction mapping using viral infectivity as a functional readout and constructed a viral host-dependency epistasis map (vE-MAP) of 356 human genes linked to HIV function, comprising >63,000 pairwise genetic perturbations. The vE-MAP
    Daniela Boassa et al.
    Cell chemical biology, 26(10), 1407-1416 (2019-08-06)
    A protein-fragment complementation assay (PCA) for detecting and localizing intracellular protein-protein interactions (PPIs) was built by bisection of miniSOG, a fluorescent flavoprotein derived from the light, oxygen, voltage (LOV)-2 domain of Arabidopsis phototropin. When brought together by interacting proteins, the
    Noemi Holderith et al.
    Cell reports, 32(4), 107968-107968 (2020-07-30)
    Elucidating the molecular mechanisms underlying the functional diversity of synapses requires a high-resolution, sensitive, diffusion-free, quantitative localization method that allows the determination of many proteins in functionally characterized individual synapses. Array tomography permits the quantitative analysis of single synapses but

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