Photographs of the F1 spikes were taken using Nikon D600 digital camera (Nikon, Tokyo, Japan), whereas those of the pistils were taken using a Nikon E995 digital camera (Nikon) mounted on a Motic K400 dissecting microscope (Preiser Scientific, Louisville, KY, USA). For cytological examination, young spikes were processed following the method described by Zhang et al.50 (link) and observed with a JSM-6360LV scanning electron microscope (JEOL, Tokyo, Japan).
Jsm 6360lv scanning
Manufactured by JEOL
Sourced in Japan
The JSM-6360LV is a scanning electron microscope (SEM) produced by JEOL. It is designed for high-resolution imaging of a wide range of samples. The JSM-6360LV utilizes a tungsten filament electron source and provides a maximum magnification of up to 300,000X. It is capable of operating in both high and low vacuum modes, allowing for the examination of a variety of specimen types.
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Lab products found in correlation
3 protocols using jsm 6360lv scanning
1
Microscopic Analysis of Plant Reproductive Structures
2
Jejunal Microscopy Examination Protocol
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The jejunal morphology were analysed using haematoxylin–eosin (H&E) staining. The images were captured and measured with computer‐assisted microscopy (Micrometrics TM; Nikon ECLIPSE E200, Tokyo, Japan).
Segments of jejunum at higher magnification were analysed using scanning electron microscopy. Treated samples were examined by a JEOL JSM‐6360LV scanning electron microscope at 25 KV. The apparent characteristics of microvillus were observed and described in the results.
Segments of jejunum at higher magnification were analysed using scanning electron microscopy. Treated samples were examined by a JEOL JSM‐6360LV scanning electron microscope at 25 KV. The apparent characteristics of microvillus were observed and described in the results.
3
Electron Microscopy of Plant Stomata
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After 4 h under experimental conditions, mature leaves at the same position from each selected plant were excised and immediately cut into small pieces. Then, they were fixed with a 4% glutaraldehyde solution and maintained at 4 °C for 12 h. Stomata on the leaves were observed with a JSM-6360LV scanning electron microscope (SEM; JEOL Ltd., Tokyo, Japan) as previously described61 (link). Chloroplasts and autophagosomes were observed on a JEOL-1230 transmission electron microscope (TEM, Hitachi, Japan) as described before23 (link),49 (link).
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