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D510 80 wide band emission filter

Manufactured by Chroma Technology
Sourced in Germany

The D510/80 wide band emission filter is a product designed for use in laboratory equipment. It is a optical filter that selectively transmits a specific range of wavelengths of light while blocking others. The core function of this filter is to isolate a desired portion of the electromagnetic spectrum for various scientific and analytical applications.

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2 protocols using d510 80 wide band emission filter

1

Lysosomal and Cytosolic Calcium Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
For lysosomal calcium measurements, we performed Oregon Green® 488 BAPTA-1 dextran (OGBD) labeling41 (link). In this assay, cells with a stable transduction of LAMP1-mRFP lentiviruses were loaded with 0.1 mg ml−1 OGBD (Invitrogen) for 30 min. For cytosolic calcium measurements, we performed X-Rhod-1 and Fura-2 labeling assays. In these assays, cells were loaded with 1 μM X-Rhod-1-AM (Invitrogen) or 1 μM Fura-2-AM (Invitrogen) for 30 min. For OGBD and X-Rhod-1 imaging, the cells were examined under a temperature- and CO2-controlled laser confocal microscope (Olympus); for ratiometric Fura-2 imaging, cells were examined under a temperature- and CO2-controlled fluorescence microscope equipped with excitation wavelengths of 340 and 380 nm (Till Polychrome V, Till Photonics, Gräfelfing, Germany), a 410-dLcp beamsplitter, a D510/80 wide band emission filter (Chroma Technology Corp., Rockingham, VT, USA) and a Quant-EM camera (Photometrics, Tucson, AZ, USA).
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2

Lysosomal and Cytosolic Calcium Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
For lysosomal calcium measurements, we performed Oregon Green® 488 BAPTA-1 dextran (OGBD) labeling41 (link). In this assay, cells with a stable transduction of LAMP1-mRFP lentiviruses were loaded with 0.1 mg ml−1 OGBD (Invitrogen) for 30 min. For cytosolic calcium measurements, we performed X-Rhod-1 and Fura-2 labeling assays. In these assays, cells were loaded with 1 μM X-Rhod-1-AM (Invitrogen) or 1 μM Fura-2-AM (Invitrogen) for 30 min. For OGBD and X-Rhod-1 imaging, the cells were examined under a temperature- and CO2-controlled laser confocal microscope (Olympus); for ratiometric Fura-2 imaging, cells were examined under a temperature- and CO2-controlled fluorescence microscope equipped with excitation wavelengths of 340 and 380 nm (Till Polychrome V, Till Photonics, Gräfelfing, Germany), a 410-dLcp beamsplitter, a D510/80 wide band emission filter (Chroma Technology Corp., Rockingham, VT, USA) and a Quant-EM camera (Photometrics, Tucson, AZ, USA).
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