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  3. BCECF-AM

BCECF-AM is a cell membrane permeable compound widely used as a fluorescent indicator for intracellular pH. BCECF-AM could diffuse through the cell membrane and intracellular esterase cleave the ester bond releasing BCECF (HY-101882). BCECF allows measurements in the physiological pH range 6.0-8.0. Excitation ratio: 490/440 nm; Emission intensity: 535 nm.

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BCECF-AM

BCECF-AM Chemical Structure

CAS No. : 117464-70-7

Size Price Stock
Solvent
205 μg (5 mM * 50 μL in DMSO) Ask For Quote & Lead Time
Solvent
410 μg (5 mM * 100 μL in DMSO) Ask For Quote & Lead Time
Solvent
820 μg (5 mM * 200 μL in DMSO) Ask For Quote & Lead Time

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Description

BCECF-AM is a cell membrane permeable compound widely used as a fluorescent indicator for intracellular pH. BCECF-AM could diffuse through the cell membrane and intracellular esterase cleave the ester bond releasing BCECF (HY-101882). BCECF allows measurements in the physiological pH range 6.0-8.0. Excitation ratio: 490/440 nm; Emission intensity: 535 nm.

In Vitro

The pH-sensitive fluorescent dyes to measure cytosolic pH[3][4].
1.Prepare a 5 mM stock solution of BCECF-AM in DMSO.
2.Prepare a 3-5 μM BCECF-AM dye-loading solution in NMG buffer (10 mM HEPES, 60 mM KCl, 3 mM MgCl2, pH 6.8) or PBS.
3. Add BCECF-AM dye-loading solution (3-5 µM) into the cell plate for 30-60 min at 37°C in the dark.
4. Cells are washed three times with PBS.
5. Run the pH assay by monitoring the fluorescence at Ex/Em = 490/535 nm or 440/535 nm for ratio measurements.

Standard Curve Determination:
1. pH calibration buffer: 130 mM KCl, 1 mM MgCl2, 15 mM HEPES, 15 mM MES (HY-D0858), 10 μM Nigericin sodium salt (HY-100381), and 10 μM Valinomycin (HY-N6693) (to balance the intracellular and extracellular pH). Adjust to pH 6.5, 7.0, 7.5, 8.0, and 8.5 with NaOH or HCl.
2. Incubate the stained cells in calibration buffer at pH 6.5, 7.0, 7.5, 8.0, and 8.5 for 10 minutes, respectively.
3. Measure the F490/F440 ratio at each pH value. Plot a standard curve with pH as the horizontal axis and fluorescence ratio as the vertical axis (this curve should be sigmoidal and can be fitted using the Henderson-Hasselbalch equation).
4. Substitute the fluorescence ratio (R) of the unknown sample measured in the experiment into the standard curve to determine the corresponding pH value.

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

Molecular Weight

820.70

Formula

C40H36O19

CAS No.
Appearance

Liquid

Color

Orange to red

Emission (Em)

528

Excitation (Ex)

503

SMILES

O=C(OCOC(C)=O)CCC1=CC(C23OC(C4=C2C=CC(C(OCOC(C)=O)=O)=C4)=O)=C(OC5=C3C=C(CCC(OCOC(C)=O)=O)C(OC(C)=O)=C5)C=C1OC(C)=O.O=C(OCOC(C)=O)CCC6=CC(C78OC(C9=C7C=C(C(OCOC(C)=O)=O)C=C9)=O)=C(OC%10=C8C=C(CCC(OCOC(C)=O)=O)C(OC(C)=O)=C%10)C=C6OC(C)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Solution, -20°C, protect from light, 2 years

Purity & Documentation

Purity: ≥99.0%

References
Cell Assay
[2]

PASMCs are placed in a laminar flow cell chamber perfused with HBSS with pH adjusted to 7.4. pHi is measured in cells incubated with the membrane permeant (acetoxymethyl ester) form of the pH-sensitive fluorescent dye BCECF-AM for 60 min at 37°C under an atmosphere of 20% O2-5% CO2. Cells are then washed with HBSS for 15 min at 37°C to remove extracellular dye and allow complete de-esterification of cytosolic dye. Ratiometric measurement of BCECF fluorescence is performed on a workstation consisting of a Nikon TSE 100 Ellipse inverted microscope with epi-fluorescence attachments. The light beam from a xenon arc lamp is filtered by interference filters at 490 and 440 nm, and focused onto the PASMCS under examination via a 20× fluorescence objective. Light emitted from the cell at 530 nm is returned through the objective and detected by an imaging camera. An electronic shutter is used to minimize photobleaching of dye. Protocols are executed and data collected on-line with InCyte software. pHi is estimated from in situcalibration after each experiment. Cells are perfused with a solution containing (in mM): 105 KCl, 1 MgCl2, 1.5 CaCl2, 10 glucose, 20 HEPES-Tris and 0.01 nigericin to allow pHi to equilibrate to external pH. A two point calibration is created from fluorescence measured as pHi is adjusted with KOH from 6.5 to 7.5. Intracellular H+ ion concentration ([H+]i) is determined from pHi using the formula: pHi = −log ([H+]i).

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

References
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Product Name:
BCECF-AM
Cat. No.:
HY-101883
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