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Vh s5

Manufactured by Keyence
Sourced in Japan

The Keyence VH-S5 is a high-speed camera designed for advanced microscopic imaging. It features a compact and lightweight design, and offers high-resolution image capture capabilities.

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5 protocols using vh s5

1

Leaf Anatomy Analysis via Paraffin Sectioning

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Freshly collected material was photographed and then fixed in FAA [100 ml FAA = 90 ml ethanol (70%) + 5 ml acetic acid 96% + 5 ml formaldehyde solution 37%] before being stored in 70% ethanol. The leaf anatomy was studied from serial sections using the classical paraffin technique and subsequent astra-blue/safranin staining (Gerlach 1984) . Macrophotography was accomplished using a digital camera (Canon PowerShot IS2) and microphotography with a digital microscope (Keyence VHX 500F) equipped with a high-precision VH mounting stand with X-Y stage and bright-field illumination (Keyence VH-S5).
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2

Macro- and Microphotography Techniques

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Macrophotography was accomplished using a digital camera (Canon PowerShot IS2) and microphotography with a digital microscope (Keyence VHX 500F) equipped with a high-precision VH mounting stand with X-Y stage and bright-field illumination (Keyence VH-S5).
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3

Leaf Anatomy Examination via Paraffin Sectioning

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Freshly collected material was photographed and then fixed in FAA (100 ml FAA = 90 ml 70% ethanol + 5 ml acetic acid 96% + 5 ml formaldehyde solution 37%) before being stored in 70% ethanol. The leaf anatomy was studied from serial sections using the classical paraffin technique and subsequent astrablue/safranin staining (Gerlach 1984) . Macrophotography was accomplished using a digital camera (Canon PowerShot IS2) and microphotography with a digital microscope (Keyence VHX 500F) equipped with a high-precision VH mounting stand with X-Y stage and bright-field illumination (Keyence VH-S5).
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4

Comprehensive Fixation and Imaging Protocol

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Freshly collected material was photographed and then fixed in FAA (100 ml FAA = 90 ml ethanol 70% + 5 ml acetic acid 96% + 5 ml formaldehyde solution 37%) before being stored in 70% ethanol. The anatomy was studied from serial sections using the classical paraffin technique and subsequent astrablue/safranin staining (Gerlach 1984) . For SEM analysis, the FAA-material was dehydrated in formaldehyde dimethyl acetal (FDA) for 24 h (Gersterberger and Leins 1978) and later critical point dried. Sputter coating was done with a Sputter Coater SCD 50 Bal-tec (Balzers). The specimens were examined with an Auriga Zeiss TM. Macrophotography was accomplished using a digital camera (Canon PowerShot IS2) and microphotography with a digital microscope (Keyence VHX 500F) equipped with a high-precision VH mounting stand with X-Y stage and bright-field illumination (Keyence VH-S5).
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5

Evaluating Mixing Dynamics via Gas Flow

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The mixing by gas flow was imaged using microbeads (diameter: 45 μm). To form a lipid bilayer, 4.2 μl of DPhPC (20 mg/ml in n-decane) was added to the wells with no microslits. Then, 25 μl of buffer solution was added to the wells with microslits, and 21 μl of buffer was added to the other wells. The 1.0 M KCl buffer solution was adjusted to pH 7.0 with 10 mM phosphate buffer. The movement of the microbeads caused by gas flow was recorded by a microscope (VH-S5, KEYENCE, Japan). The gas flow rate was monitored by a flow meter. We used PIV to evaluate the mixing in the droplet. Tracers (diameter: 10 μm; Kato Koken, Japan) were dispersed at 0.1% solid concentration. The experimental system is composed of a 16-channel gas flow device, a visualization laser (PIV Laser G2000, Kato Koken, Japan), and a high-speed camera (k8-USB, Kato Koken, Japan). The laser irradiated a laser sheet (thickness: 2 mm) in a direction parallel to the gas flow device. The high-speed camera was placed above the gas flow device to obtain top-view images. We used four N2 gas flow conditions: 0, 0.1, 0.2, and 0.3 liters/min. The direct cross-correlation method was used for vector calculation using PIV analysis software (Flow Expert 2D2C, Kato Koken, Japan) (30 ). The differences in particle velocities were evaluated quantitatively depending on the particle position and the gas flow rate.
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