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About This Item
Empirical Formula (Hill Notation):
C22H17BrO2
CAS Number:
Molecular Weight:
393.27
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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+
SMILES string
Oc1ccc(cc1)\C=C\c2ccc(\C=C\c3ccc(O)cc3)c(Br)c2
InChI key
OXPHQQMZTXMEGO-RJTULKDBSA-N
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: soluble >10 mg/mL
storage temp.
2-8°C
Quality Level
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.
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.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Eye Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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