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About This Item
Empirical Formula (Hill Notation):
C28H23N3O5
CAS Number:
Molecular Weight:
481.50
UNSPSC Code:
12352116
NACRES:
NA.32
MDL number:
Quality Level
assay
≥85% (HPLC)
form
powder
solubility
DMSO: soluble, methanol: soluble
fluorescence
λex 543 nm; λem 575 nm in 0.1 M phosphate pH 7.0
suitability
suitable for fluorescence
storage temp.
−20°C
SMILES string
N5(C(=O)C=CC5=O)c1cc(c(cc1)C2=C3CC=C(C=C3Oc4c2ccc(c4)N(C)C)N(C)C)C(=O)O
InChI
1S/C28H25N3O5/c1-29(2)16-5-9-20-23(14-16)36-24-15-17(30(3)4)6-10-21(24)27(20)19-8-7-18(13-22(19)28(34)35)31-25(32)11-12-26(31)33/h5-9,11-15H,10H2,1-4H3,(H,34,35)
InChI key
KGFLZYXDJDOIEE-UHFFFAOYSA-N
Application
Tetramethylrhodamine-5-maleimide has been used:
- to concentrate the eluate and in labeling to create IRE1LDS112C
- to derivatize green fluorescent protein (GFP) on Cys48 for experiments with the extrinsic fluorescent probe
- to incubate the single solvent exposed cys mutant to perform protein labeling
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
Labeling reagent for protein thiols for cytofluorescence
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Cytofluorescence techniques for the visualization of distinct pools of protein thiols at the single cell level.
Alfonso Pompella et al.
Methods in molecular biology (Clifton, N.J.), 196, 305-312 (2002-08-03)
Effect of the point mutation H148G on GFPmut2 unfolding kinetics by fluorescence spectroscopy
Bosisio C, et al.
Biophysical Chemistry, 157(1-3), 24-32 (2011)
Specific stereochemistry of OP-1074 disrupts estrogen receptor alpha helix 12 and confers pure antiestrogenic activity
Fanning SW, et al.,
Nature Communications, 9(1), 2368-2368 (2018)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 94506-1MG-F | 04061826670385 |
| 94506-5MG-F | 04061833276822 |