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Tetracysteine REASH acetate *2 mM DMSO Solution*

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Physical properties
Molecular weight587.40
SolventDMSO
Spectral properties
Absorbance (nm)570
Extinction coefficient (cm -1 M -1)650001
Excitation (nm)571
Emission (nm)584
Quantum yield0.751
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12171501

OverviewpdfSDSpdfProtocol


Molecular weight
587.40
Absorbance (nm)
570
Extinction coefficient (cm -1 M -1)
650001
Excitation (nm)
571
Emission (nm)
584
Quantum yield
0.751
REASH acetate is a cell-permeable version of REASH, which is a resorufin derivative, modified to contain two arsenic atoms at a set distance from each other. The biarsenical labeling technology works through the high-affinity interaction of arsenic for thiols. When REASH binds to tetracysteine sequences, its biarsenical group reacts rapidly with Cys-Cys moiety and the tag become highly fluorescent in red. The biarsenical labeling reagent REASH is one of the smallest expression tags for labeling a protein that contains a six-amino acid motif with a Cys-Cys-X1-X2-Cys-Cys amino acid sequence. The most commonly used tetracysteine is the six amino acid Cys-Cys-Pro-Gly-Cys-Cys sequence. As this sequence rarely appears in endogenous proteins, incorporating the sequence into target proteins generates a small but highly specific target for protein labeling. REASH generates a strong red fluorescent signal when binding to recombinant proteins containing the tetracysteine motif Cys-Cys-Pro-Gly-Cys-Cys. It can be used for monitoring protein localization, turnover and trafficking, receptor signaling and internalization.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Tetracysteine REASH acetate *2 mM DMSO Solution* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM170.242 µL851.209 µL1.702 mL8.512 mL17.024 mL
5 mM34.048 µL170.242 µL340.483 µL1.702 mL3.405 mL
10 mM17.024 µL85.121 µL170.242 µL851.209 µL1.702 mL

Molarity calculator

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Spectrum


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spectrum

Spectral properties

Absorbance (nm)570
Extinction coefficient (cm -1 M -1)650001
Excitation (nm)571
Emission (nm)584
Quantum yield0.751

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yield
Tetracysteine REASH Reagent *2 mM DMSO Solution*5715846500010.751

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References


View all 4 references: Citation Explorer
Discrete Virus Factories Form in the Cytoplasm of Cells Coinfected with Two Replication-Competent Tagged Reporter Birnaviruses That Subsequently Coalesce over Time.
Authors: Campbell, Elle A and Reddy, Vishwanatha R A P and Gray, Alice G and Wells, Joanna and Simpson, Jennifer and Skinner, Michael A and Hawes, Philippa C and Broadbent, Andrew J
Journal: Journal of virology (2020)
Exploration of biarsenical chemistry--challenges in protein research.
Authors: Pomorski, Adam and Krężel, Artur
Journal: Chembiochem : a European journal of chemical biology (2011): 1152-67
Tetracysteine-based fluorescent tags to study protein localization and trafficking in Plasmodium falciparum-infected erythrocytes.
Authors: Crivat, Georgeta and Tokumasu, Fuyuki and Sa, Juliana Martha and Hwang, Jeeseong and Wellems, Thomas E
Journal: PloS one (2011): e22975
Tetracysteine genetic tags complexed with biarsenical ligands as a tool for investigating gap junction structure and dynamics.
Authors: Sosinsky, Gina E and Gaietta, Guido M and Hand, Galen and Deerinck, Thomas J and Han, Areum and Mackey, Mason and Adams, Stephen R and Bouwer, James and Tsien, Roger Y and Ellisman, Mark H
Journal: Cell communication & adhesion : 181-6