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  3. DFHBI-1T (solution)

DFHBI-1T (solution) is a membrane-permeable RNA aptamers-activated fluorescence probe (ex/em=472 nm/507 nm). DFHBI-1T binds to RNA aptamers (Spinach, Spinach2, iSpinach, and Broccoli) and causes specific fluorescence and lower background fluorescence. DFHBI-1T is used to image RNA in live cells.
Solution Concentration: 20 mM

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

DFHBI-1T (solution)

DFHBI-1T (solution) Chemical Structure

CAS No. : 1539318-36-9

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200 μL Ask For Quote & Lead Time

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Description

DFHBI-1T (solution) is a membrane-permeable RNA aptamers-activated fluorescence probe (ex/em=472 nm/507 nm). DFHBI-1T binds to RNA aptamers (Spinach, Spinach2, iSpinach, and Broccoli) and causes specific fluorescence and lower background fluorescence. DFHBI-1T is used to image RNA in live cells[1][2].
Solution Concentration: 20 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).
1.1 Stock solution[1]
It is recommended that the DFHBI-1T stock solution be stored at -20℃ or -80℃ in the dark after aliquoting.
1.2 Preparation of working solution
Dilute the stock solution with serum-free medium. The corresponding stock solution can be diluted according to the actual situation. Note that if the solvent is DMSO, the cytotoxicity of DMSO must be considered, and a solvent control should be prepared; if the solvent is pure water, the working solution needs to be filtered and sterilized before adding cells.
Note: Please adjust the concentration of DFHBI-1T working solution according to actual conditions and prepare it before use.
2 Specific staining steps
1) Inoculate cells expressing Spinach2-tagged RNA in a suitable culture dish or culture plate and culture under standard cell culture conditions. 2) Aspirate the old medium and gently wash the cells twice with pre-warmed PBS to remove residual serum and cell debris.
3) Add 20 μM DFHBI-1T working solution to the cells, ensuring complete coverage of the cell monolayer.
4) Incubate the cells with the dye for 10 min in a 37°C, 5% CO2 humidified incubator.
5) After incubation, aspirate the dye-containing medium and wash the cells three times with pre-warmed PBS to remove unbound DFHBI-1T.
6) Replace PBS with fresh cell culture medium or imaging buffer.
7) Immediately image the cells using a fluorescence microscope equipped with a GFP filter set to detect fluorescence of the Spinach2-DFHBI-1T complex.

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

Molecular Weight

320.21

Formula

C13H9F5N2O2

CAS No.
SMILES

O=C1N(C(C)=N/C1=C\C2=CC(F)=C(C(F)=C2)O)CC(F)(F)F

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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DFHBI-1T (solution) Related Classifications

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DFHBI-1T (solution)
Cat. No.:
HY-DY1047
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