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Deltaram excitation light source

Manufactured by Horiba

The DeltaRAM excitation light source is a versatile instrument designed to provide high-quality, tunable light for a variety of spectroscopic applications. It offers a wide range of wavelength options, allowing users to select the optimal excitation wavelength for their specific research or analytical needs.

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2 protocols using deltaram excitation light source

1

Ca2+ Imaging of TRPM3 Channels

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Ca2+ imaging experiments were performed using an Olympus IX-51 inverted microscope equipped with a DeltaRAM excitation light source (Photon Technology International, PTI), as described earlier (Badheka et al., 2017 (link)). HEK293 cells were transfected with hTRPM3α2-GFP or its mutants using the Effectene reagent (Qiagen). Cells were loaded with 1 μM fura-2 AM (Invitrogen) for 40 min before the measurements at 37°C, and dual-excitation images at 340 and 380 nm excitation wavelengths were detected at 510 nm with a Roper Cool-Snap digital CCD camera. Measurements were conducted at room temperature in extracellular solution containing 137 mM NaCl, 5 mM KCl, 1 mM MgCl2, 2 mM CaCl2, 10 mM HEPES and 10 mM glucose, pH 7.4. PregS, and primidone were applied with a gravity-driven whole chamber perfusion system. Temperature stimulation was performed using a custom-built system as described earlier (Badheka et al., 2017 (link)) by pushing bath solution through a spiral tubing immersed in hot water using a 60 ml syringe while monitoring the temperature of the perfusion chamber using a CL-100 Warner Instruments temperature controller. The analogue signal from the CL-100 unit was fed into the Digidata digitizer and the temperature curve was collected in Clampex. Data analysis was performed using the Image Master 5 software (PTI).
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2

Calcium Imaging of DRG Neurons

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Ca2+ imaging measurements were performed with an Olympus IX-51 inverted microscope equipped with a DeltaRAM excitation light source (Photon Technology International, PTI), as described earlier (Lukacs et al., 2013 (link)). Briefly, DRG neurons or HEK cells were loaded with 1 μM fura-2 AM (Invitrogen) for 40 min before the measurement at 37°C, and dual-excitation images at 340 and 380 nm excitation wavelengths were detected at 510 nm with a Roper Cool-Snap digital CCD camera. Measurements were conducted in the same bath solution we used for whole-cell patch clamp, supplemented with 2 mM CaCl2. PregS, baclofen, somatostatin and CIM0216 were applied with a gravity driven whole chamber perfusion system. Data analysis was performed using the Image Master software (PTI).
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