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Sp5 mp microscope

Manufactured by Leica

The Leica SP5 MP microscope is a high-performance confocal laser scanning microscope designed for advanced imaging applications. It features a multi-photon excitation capability, allowing for deep tissue imaging and reduced phototoxicity. The instrument's core function is to provide researchers with a versatile and powerful tool for capturing detailed, high-resolution images of a wide range of biological samples.

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2 protocols using sp5 mp microscope

1

Multiphoton Microscopy Imaging of Ear Tissue

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MPM imaging was performed as described48 (link). Briefly, images were acquired on an upright Leica SP5 MP microscope (Leica Microsystems) equipped with two Mai Tai Ti:Sapphire lasers (Spectra Physics) and 10-Watt pumps or on an inverted Leica TCS SP8 MP microscope (Leica Microsystems). Ears were immobilized on an imaging platform and bathed in warm saline. All images were acquired using a 20x objective (NA 1.00). Emitted fluorescence was collected with a four-channel non-descanned detector. For blue/green channels, wavelength separation was accomplished with a dichroic mirror at 495 nm followed by emission filters of 460/50 nm bandpass and 525/50 nm bandpass. Second harmonic generation of collagen in the dermis is shown in blue according to convention. Tile-scans of 8 fields of view were collected covering approximately 2.8 mm of the ear. Sequences of image stacks were transformed into maximum intensity projections using Imaris software (Bitplane).
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2

Multiphoton Microscopy Imaging of Ear Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols
MPM imaging was performed as described48 (link). Briefly, images were acquired on an upright Leica SP5 MP microscope (Leica Microsystems) equipped with two Mai Tai Ti:Sapphire lasers (Spectra Physics) and 10-Watt pumps or on an inverted Leica TCS SP8 MP microscope (Leica Microsystems). Ears were immobilized on an imaging platform and bathed in warm saline. All images were acquired using a 20x objective (NA 1.00). Emitted fluorescence was collected with a four-channel non-descanned detector. For blue/green channels, wavelength separation was accomplished with a dichroic mirror at 495 nm followed by emission filters of 460/50 nm bandpass and 525/50 nm bandpass. Second harmonic generation of collagen in the dermis is shown in blue according to convention. Tile-scans of 8 fields of view were collected covering approximately 2.8 mm of the ear. Sequences of image stacks were transformed into maximum intensity projections using Imaris software (Bitplane).
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