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  3. TPE-MI (solution)

TPE-MI (Tetraphenylethene maleimide) (solution) is a thiol probe for measuring unfolded protein load and proteostasis in cells (the excitation wavelength is 350 nm and the emission wavelength is 470 nm). TPE-MI can report imbalances in proteostasis in induced pluripotent stem cell models of Huntington disease, as well as cells transfected with mutant Huntington exon 1 before the formation of visible aggregates. TPE-MI also detects protein damage following dihydroartemisinin research of the malaria parasitesPlasmodium falciparum .
Solvent and concentration: DMSO: 10 mM

For research use only. We do not sell to patients.

TPE-MI (solution)

TPE-MI (solution) Chemical Structure

CAS No. : 1245606-71-6

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Solvent
50 μL Ask For Quote & Lead Time
Solvent
100 μL Ask For Quote & Lead Time

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Description

TPE-MI (Tetraphenylethene maleimide) (solution) is a thiol probe for measuring unfolded protein load and proteostasis in cells (the excitation wavelength is 350 nm and the emission wavelength is 470 nm). TPE-MI can report imbalances in proteostasis in induced pluripotent stem cell models of Huntington disease, as well as cells transfected with mutant Huntington exon 1 before the formation of visible aggregates. TPE-MI also detects protein damage following dihydroartemisinin research of the malaria parasitesPlasmodium falciparum [1][2].
Solvent and concentration: DMSO: 10 mM

In Vitro

Guide (The following is our recommended protocol. This protocol is only a guide and should be modified according to your specific needs).
1 Stock solution[1]
Dissolve TPE-MI in DMSO to make a 1 mM to 50 mM stock solution.
2 Preparation of dye working solution
1) Dilute the stock solution to a working concentration (typically 50 μM) in PBS before use.
Note: Please adjust the concentration of TPE-MI working solution according to the actual situation and prepare it before use.
3 Specific staining steps
1) Cell culture preparation: Seed cells (e.g. HeLa, Neuro2a cells) in a suitable culture container (e.g. 8-well μ-slides).
2) Washing: Wash cells with PBS and remove culture medium.
3) Staining: Add 50 μM TPE-MI working solution to the cells and incubate at 37 °C for 30 min.
4) Post-staining treatment:
Flow cytometry: Remove TPE-MI solution, digest the cells using appropriate methods (such as trypsin digestion, Accutase) , resuspend in PBS and centrifuge (120 g, 6 min) , discard the supernatant, and resuspend the cells in PBS for analysis.
SDS-PAGE detection: Lyse the stained cells with cell lysis buffer, determine the protein concentration, and perform fluorescence and Coomassie brilliant blue staining analysis after 12% polyacrylamide SDS-PAGE electrophoresis.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

441.53

Formula

C31H23NO2

CAS No.
SMILES

O=C(C=C1)N(C2=CC=C(/C(C3=CC=CC=C3)=C(C4=CC=C(C)C=C4)/C5=CC=CC=C5)C=C2)C1=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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TPE-MI (solution)
Cat. No.:
HY-DY1024
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