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Stompm microscope

Manufactured by Thorlabs

The STOMPM microscope is a specialized imaging instrument designed for high-resolution observation and analysis. It utilizes a combination of techniques, including scanning tunneling microscopy (STM) and optical microscopy, to provide detailed topographical and electronic information about sample surfaces at the nanoscale level. The core function of the STOMPM microscope is to enable the visualization and study of nanoscale structures and phenomena, allowing users to gain insights into the physical and chemical properties of their samples.

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Lab products found in correlation

3 protocols using stompm microscope

1

Intrinsic Hemodynamic Imaging of Visual Cortex

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Intrinsic signal imaging was performed on the STOMPM microscope or on the Thorlabs Bergamo II. The cortex was illuminated with blue light to obtain a blood vessel map, after which collimated 630 nm light from an LED (Thorlabs) was directed onto the surface of the brain to measure intrinsic hemodynamic responses. Visually evoked responses were collected at 50 Hz using an Andor Xyla camera. Visual stimuli were blockwise grating stimuli (8s on, 8s off, 0.06-0.1 cycles per degree, 16 directions).
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2

Intrinsic Signal Imaging of Cortical Hemodynamics

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Intrinsic signal imaging was performed on the STOMPM microscope or on the Thorlabs Bergamo II. The cortex was illuminated with blue light to obtain a blood vessel map, after which collimated 630 nm light from an LED (Thorlabs) was directed onto the surface of the brain to measure intrinsic hemodynamic responses. Visually evoked responses were collected at ~50 Hz using an Andor Xyla camera. Visual stimuli were blockwise grating stimuli (8s on, 8s off, .06-.1 cycles per degree, 16 directions).
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3

Intrinsic Signal Imaging of Cortical Hemodynamics

Check if the same lab product or an alternative is used in the 5 most similar protocols
Intrinsic signal imaging was performed on the STOMPM microscope or on the Thorlabs Bergamo II. The cortex was illuminated with blue light to obtain a blood vessel map, after which collimated 630 nm light from an LED (Thorlabs) was directed onto the surface of the brain to measure intrinsic hemodynamic responses. Visually evoked responses were collected at ~50 Hz using an Andor Xyla camera. Visual stimuli were blockwise grating stimuli (8s on, 8s off, .06-.1 cycles per degree, 16 directions).
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