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Key Documents

K1015

Sigma-Aldrich

K114

≥98% (HPLC), powder

Synonym(s):

(trans,trans)-1-Bromo-2,5-bis-(4-hydroxy)styrylbenzene

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About This Item

Empirical Formula (Hill Notation):
C22H17BrO2
CAS Number:
Molecular Weight:
393.27
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Quality Level

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: soluble >10 mg/mL

storage temp.

2-8°C

SMILES string

Oc1ccc(cc1)\C=C\c2ccc(\C=C\c3ccc(O)cc3)c(Br)c2

InChI

1S/C22H17BrO2/c23-22-15-18(2-1-16-5-11-20(24)12-6-16)4-10-19(22)9-3-17-7-13-21(25)14-8-17/h1-15,24-25H/b2-1+,9-3+

InChI key

OXPHQQMZTXMEGO-RJTULKDBSA-N

Biochem/physiol Actions

K114 is a fluorescent, amyloid-specific dye, an analogue of Congo Red and BSB that recognizes amyloid lesions and allows the quantitative monitoring of the formation of amyloid fibrils assembled from the Aβ peptide, α-synuclein, and tau. The affinity for fibrils ranges 20-30 nM. Unlike the other compounds K114 has minimal fluorescence in aqueous buffers, but fluoresces brightly in the presence of amyloid fibrils. K114 can be used to monitor in vitro amyloid fibril formation by fluorescence emission at 550 nm.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Eric B Dammer et al.
PloS one, 7(6), e38658-e38658 (2012-07-05)
TAR DNA-binding protein 43 (TDP-43) is a major component within ubiquitin-positive inclusions of a number of neurodegenerative diseases that increasingly are considered as TDP-43 proteinopathies. Identities of other inclusion proteins associated with TDP-43 aggregation remain poorly defined. In this study
Tak-Ho Chu et al.
Journal of Alzheimer's disease : JAD, 77(3), 1315-1330 (2020-09-15)
Axonal injury has been implicated in the development of amyloid-β in experimental brain injuries and clinical cases. The anatomy of the spinal cord provides a tractable model for examining the effects of trauma on amyloid deposition. Our goal was to

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