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Axio lsm700

Manufactured by Zeiss
Sourced in Germany

The Axio LSM700 is a laser scanning microscope developed by Zeiss. It is designed for high-resolution imaging and analysis of a wide range of samples. The core function of the Axio LSM700 is to provide advanced optical imaging capabilities through the use of laser technology.

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4 protocols using axio lsm700

1

Comprehensive Characterization of Material Surfaces

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The morphologies and structures of the samples were characterized by a field emission SEM (MIRA3 LMU, TESCAN, Czech Republic). The chemical compositions and elemental maps were determined using energy‐dispersive X‐ray spectroscopy (EDS, TESCAN, Czech Republic). The 3D surface morphologies and cross‐sectional profiles were taken by LCM (Axio LSM700, Zeiss, Germany). A UV–vis spectrophotometer (UV‐2600, Japan) with an integrating sphere was used to investigate the transmissivity and reflectivity of samples in the range of 220–1400 nm. The contact angles of different liquid droplets were measured with a contact angle measurement system (Biolin Scientific, Finland). The average contact angles and standard deviations were calculated by measuring five droplets at different locations on the same sample surface.
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2

Multimodal Characterization of Micro-/Nanostructures

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A field emission scanning electron microscope (SEM, MIRA3 LMU, Tescan, Czech Republic) was utilized to observe the micro-/nanostructures. The elemental composition and map of the samples were determined by an energy-dispersive spectroscope (EDS, Tescan, Czech Republic). The three-dimensional morphology and cross-sectional profiles were characterized by a laser confocal microscope (LCM; Axio LSM700, Zeiss, Germany). The surface temperature distribution was recorded by an infrared camera (Ti450, Fluke, USA). A contact angle system (Biolin Scientific, Finland) was used to measure the contact angles of water droplets on the samples surfaces. The left and right contact angles were measured to calculate the average value of water contact angles (WCAs). All average WCAs and standard deviations were calculated from at least three different measurements.
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3

Corrosion Morphology and Composition Analysis

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In order to better observe the corrosion morphology of the specimen surface and analyze the elements of the corrosion products, the surface of the specimens was first dried with a compressed air gun and then was observed by scanning electron microscope (SEM) (EvoMA 10C Zeissi Jena, Oberkochen, Germany). Moreover, the chemical elements of the surface corrosion products were analyzed by energy disperse spectroscopy (EDS) and the surface morphology of corrosion specimens is obtained by using Hyperfield 3D microscopic systems (Keyence VHX-5000, Osaka, Japan) and confocal laser scanning microscopy (CLSM) (Zeiss Axio LSM700, Oberkochen, Germany).
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4

Fluorescent Imaging of Worm Anatomy

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Worms of the desired age were mounted on 1% agarose pads in 20 mM sodium azide. Fluorescent imaging was carried out using a Zeiss Imager.M2 microscope at 63× magnification. Images were taken using the Zeiss Zen 2012 Blue Software at 7.4 pixels/µm and representative images compiled using Adobe Photoshop 7.0. Confocal imaging of worms was undertaken on an inverted Zeiss Axio LSM700 equipped with a 488 nm diode laser and LP490 filter. Images were taken at x40 magnification, 1024 × 1024 resolution, with 4× averaging and a Z-stack slice of 1 µm. Stacks were made through the head region of the full animal to encompass all of the fluorescent signal, and then compressed to a maximum projection with Zen Blue 2011 SP3 v8.1 software at 6.4 pixels/µm and compiled in Adobe Photoshop 7.0.
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