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Merck
CN

K1015

Sigma-Aldrich

K114

≥98% (HPLC), powder

别名:

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

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关于此项目

经验公式(希尔记法):
C22H17BrO2
化学文摘社编号:
分子量:
393.27
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: soluble >10 mg/mL

储存温度

2-8°C

SMILES字符串

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

生化/生理作用

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.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 4 - Eye Irrit. 2

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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