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PBX Calcium Assay Kit (For Probenecid Sensitive Assays)

PBX Calcium Assay Kit (For Probenecid Sensitive Assays)

(RUO)
Product Details
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BD™
Functional assay (Routinely Tested)
RUO


Description

Components:        Calcium Indicator, 1 vial, lyophilized

        10X PBX Signal Enhancer, 10 ml

        Calcium Assay Buffer, 90 ml

The BD™ PBX Calcium Assay Kit allows homogeneous measurement of intracellular calcium changes caused by activation of G-protein coupled receptors or calcium channels. The assay involves only one dye addition step and does not require washing, allowing easy implementation in a high-throughput environment. Probenecid, a standard inhibitor of nonspecific anion transport, is not required for dye-loading into CHO, Hela and BD™ ACTOne cell lines with this kit, but can improve retention of the dye in cells.

Preparation And Storage

Calcium Indicator should be protected from light and stored at -20°C. 10X PBX Signal Enhancer and Calcium Assay Buffer should be stored at room temperature.

Recommended Assay Procedures

CALCIUM FLUX ASSAY PROTOCOL

Note. Please finish reading the entire protocol before you start the experiment.

Materials not included

100% DMSO                 Sigma D4540

Probenecid (Optional)        Sigma P8761

CELL PREPARATION

Cell number needs to be optimized for each assay. Optimal assay conditions require a confluent monolayer of cells prior to the assay.

        -For adherent cells, plate 50K to 70K cells/well for a 96 well plate and 12K to 20K cells/well for a 384 well plate the day before the experiment. Add 100 µl/well of cell suspension to 96-well plates or 25  l/well to 384-well plates, allow cells to attach and grow overnight for 16 to 24 hours in cell culture incubators. Prior to dye loading the plate, examine the cells for confluency and overall health.

        -For non-adherent cells, dispense 100  µl/well of cells in culture medium to 96-well or 25  µl/well to 384-well poly-D Lysine or other ECM coated plates a couple of hours before the experiment. Allow cells to settle and attach to the bottom of the plates at room temperature. Centrifuge briefly with brake off prior to the experiment.

PREPARATION of 1X DYE-LOADING SOLUTION

1.        Remove a vial of Calcium Indicator from -20°C, and allow to sit at room temperature for 5 minutes to warm up. Add 100 µl 100% DMSO, reconstitute the pellet by pipetting up and down several times.

Note. To completely solublize the Calcium Indicator, keep the reconstituted Calcium Indicator at room temperature for 10 minutes before the preparation of 1X Dye-loading solution.

2.        To prepare 1X PBX Signal Enhancer, transfer 10 ml of 10X PBX Signal Enhancer to 90 ml of 1X Calcium Assay buffer, mix well.

Note. Probenecid is not essential for dye-loading, although it often improves retention of the dye in cells. For cells that require probenecid for loading (e.g. CHO), prepare fresh probenecid stock in 1N NaOH and then dilute the stock in 1X PBX Signal Enhancer to a concentration of 1 mM to 5 mM if desired.

3.        To prepare 1X Dye-loading Solution for one cell plate, pipette 10 ml of 1X PBX Signal Enhancer to a separate tube, add 10 µl of Calcium Indicator to 10 ml of 1X PBX Signal Enhancer, mix by inverting the tube several times.

4.        Aliquot the unused Calcium Indicator to several microfuge tubes, seal tightly and store at -20°C. 1X PBX Signal Enhancer could be stored at room temperature.

Note. The reconstituted Calcium Indicator is stable for more than one month if the tube is sealed tightly. For best result, place the tubes in a zip lock plastic bag with desiccant and avoid repetitive freeze-thaw cycles.

DYE LOADING

1.        Remove cell plates from incubator and add an equal volume of 1 X Dye-loading Solution to each well (e.g. 100  l to 100  l culture medium/well for 96-well plates, or 25  l to 25  l culture medium/well for 384-well plates).

Note. The components of the kit have no interference with serum or phenol red. However, for some assays that require a serum free environment, culture medium that contains serum should be removed prior to dye loading and replaced with an equal volume of 0.5X Dye-loading Solution.

The 1x dye-loading solution is stable for 8 to 12 hours at room temperature and 2-3 weeks at -20C.

2.        Incubate cell plates with dye for 1 hour in cell culture incubator.

Note. If the calcium flux assay is going to be performed at room temperature, place the cell plates at room temperature for at least 20 minutes to cool down before placing the plates on readers. If the calcium flux assay requires 37°C, perform the assay immediately after dye-loading.

CALCIUM FLUX ASSAY

Place the cell plates on a FLIPR, FlexStation or FDSS, and perform calcium flux assay as described in instrumentation manuals.

For assays performed on a FlexStation, use the following wavelength parameters:

Excitation:  485 nm                 

Emission:  525 nm

AutoCutoff:  on (515 nm)

For assays performed on a FLIPR and an FDSS, use the standard filters for calcium assays.

Note. Dispense speed and height for compound additions need to be optimized for each assay. In general, a dispense speed higher than the settings for other calcium flux assays is recommended.

TROUBLESHOOTING GUIDE

1.        Low baseline fluorescent signal

"        Inspect the cell density and morphology under a microscope. Low cell density or unhealthy cells could result in low baseline signal.

"        Check the storage of Calcium Indicator. Calcium Indicator needs to be stored in a tightly sealed tube frozen with desiccant. Once it is

        reconstituted, repetitive freeze thaw cycles should be avoided.  

"        Make sure that Calcium Indicator is mixed well with 1X PBX Signal Enhancer before dye loading.

2.        Response to agonist lower than expected

"        Check the overall health of cells.

"        Cell density is too high or too low. Cell number titration may be necessary.  

3.        Well-to-well variations after agonist addition.

"        Optimize the dispense height and speed for ligand additions to ensure instant mixing.

"        Cells should be evenly distributed among wells. Before plating, microscopically examine the culture to be sure that they have been broken up

        into single cells. Clumpy cells respond with greater variability.

"        Check liquid handling system for accuracy of dispense.

4.        Response from cells after buffer addition.

"        Unhealthy cells could respond to buffer addition. Make sure cells are not over confluent or unhealthy before plating.

"        Cells are disturbed by high compound addition speed. Set the pipetting speed and height properly to avoid stimulating the cells by physical

        forces during compound addition.

5.        Response from cells after the addition of buffer containing only DMSO

"        If the calcium flux experiment is conducted at room temperature, allow the cell plates to equilibrate at room temperature for a longer period of

        time (ie. one hour) after dye-loading at 37 degree.

"        Allow cells to adapt to a DMSO environment prior to drug addition by adding DMSO in Dye-loading Solution (slightly less than final

        concentration of DMSO after drug addition).

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
640175 Rev. 1

Please refer to Support Documents for Quality Certificates

Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.

Comparisons, where applicable, are made against older BD technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.