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Szx2 illb stereomicroscope

Manufactured by Olympus
Sourced in Japan

The SZX2-ILLB is a stereomicroscope designed for versatile imaging and observation applications. It features a parfocal zoom system with a magnification range of 6.3x to 63x, providing clear and detailed views of specimens. The microscope is equipped with an LED illumination system for consistent and even illumination.

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9 protocols using szx2 illb stereomicroscope

1

Maize Mutant ms33-6038 Characterization

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The ms33-6038 (No. 228I) mutant was initially obtained from the Maize Genetics Cooperation Stock Center (http://maizecoop.cropsci.uiuc.edu, accessed on 20 July 2014). All plant materials were grown at the experimental station of USTB in Beijing. Photos of WT and ms33-6038 tassels were taken by a Canon EOS 700D camera (Canon, Tokyo, Japan). Fresh anthers of WT and ms33-6038 at stages S8b and S9 were photographed using an SZX2-ILLB stereomicroscope (Olympus, Tokyo, Japan). Pollen grains were stained with 1% I2-KI and photographed using a BX-53F microscope (Olympus, Japan).
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2

Imaging and Pollen Grain Analysis

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A Canon EOS 700D digital camera (Canon, Tokyo, Japan) and a SZX2-ILLB stereomicroscope (Olympus, Tokyo, Japan) were used to take photographs for tassels and anthers, respectively. A BX-53 microscope (Olympus, Tokyo, Japan) was used to assay its mature pollen grains with 1% I2-KI solution [25 (link)].
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3

Characterization of ms20 Maize Mutant

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The ms20 (No. 928C) mutant seeds were originally obtained from the Maize Genetics Operation Stock Center (http://maizecoop.cropsci.uiuc.edu). All the plant materials were grown in the experiments stations of University of Science and Technology Beijing (USTB) in Beijing and Hainan Province. Tassels were photographed with an EOS 7000 digital camera (Canon, Tokyo, Japan). Anthers and pollen grains stained with 1% I2-KI solution were photographed with a SZX2-ILLB stereomicroscope (Olympus, Tokyo, Japan) and BX-53F microscope (Olympus, Tokyo, Japan), respectively.
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4

Maize Genetics Cooperation Stock Center Mutant Seeds

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The ms13 (No. 501D) and ms13-6060 (No. 503G) mutant seeds were originally obtained from Maize Genetics Cooperation Stock Center (https://maizecoop.cropsci.uiuc.edu/). All the plants were grown at the experimental stations of University of Sciences and Technology Beijing (USTB) in Beijing and Sanya, China. Tobacco (Nicotiana benthamiana) plants were grown in the light incubator with 16 h of light and 8 h of dark at 22 °C. Photos of maize tassels and plants were taken with a Canon EOS 700D digital camera (Canon, Japan). Anthers and pollen grains stained with 1 % I2-KI solution were photographed by SZX2-ILLB stereomicroscope and BX-53F microscope (Olympus, Japan), respectively.
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5

Zea mays Male Sterility Genetics

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Two homozygous knockout lines of Zm00001d013960 (ZmMs13-Cas9-6 and −7) were crossed and pollinated by ZmMs13/ms13-6060 heterozygous plants. Then the ratio of male fertile to sterile plants was counted and analyzed to determine whether it follows the theoretical segregation ratio of 1:1. The pictures of F1 pollen grains stained with 1 % I2- KI solution were taken by SZX2-ILLB stereomicroscope (Olympus, Japan).
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6

Maize Transcriptional Regulator Knockout

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Maize inbred line B73 and the parental lines (Hi A and B) of hybrid Hi II were obtained from the Maize Genetics Cooperation Stock Center (http://maizecoop.cropsci.uiuc.edu). Maize CRISPR/Cas9 knockout line myb84 was produced previously and maintained in our laboratory (Jiang et al., 2021a (link),b (link)). All plants were grown at the experimental stations of the University of Science and Technology Beijing (USTB) in Beijing and Sanya, China. The T0 transgenic plants were grown in a greenhouse under long‐day conditions (16 h/8 h (day/night) at 26 °C/22 °C). Images of the tassels and anthers were captured with a Canon EOS 700D digital camera and a SZX2‐ILLB stereomicroscope (Olympus, Tokyo, Japan), respectively. Pollen grains stained with 1% I2‐KI solution were photographed using BX‐53F microscope (Olympus).
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7

Analysis of Anther and Pollen Morphology

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Images of the tassels and anthers were captured with a Canon EOS 700D digital camera (Canon, Tokyo, Japan) and a SZX2-ILLB stereomicroscope (Olympus, Tokyo, Japan) respectively. Routine analysis of I2-KI staining and SEM (scanning electron microscopy) were performed as described previously [44 (link)]. SEM images of anther and pollen grain were detected with a HITACHI S-3400N scanning electron microscope (HITACHI, Tokyo, Japan).
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8

Maize Inbred Lines and Hybrid Analysis

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Maize inbred lines B73, Zheng 58 and M6007 and hybrid Hi II were used in this study. B73 and M6007, corresponding to the WT lines of maize GMS mutants lob30 and ms7‐6007, respectively, were originally obtained from the Maize Genetics Cooperation Stock Center (http://maizecoop.cropsci.uiuc.edu). Zheng58 and Hi II are maintained in our laboratory. All plants were grown in the experimental stations of the University of Sciences and Technology Beijing (USTB) in Beijing and Sanya, excepting T0 transgenic plants that were grown in a greenhouse under long‐day conditions (16 h/8 h (day/night) at 26 °C/22 °C). A Canon EOS 700D digital camera and an SZX2‐ILLB stereomicroscope (Olympus, Japan) were used to photograph the images of tassels and anthers, respectively. Pollen grains were stained with a 1% I2‐KI solution and captured using an Olympus SZ51 microscope (Olympus, Japan) (Zhang et al., 2018a (link)).
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9

Embryo and Larval Phenotyping Microscopy

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Phenotypic evaluation of embryos and larvae was performed using an Olympus SZX2-ILLB stereomicroscope (Olympus Corporation, Japan). Images were captured with an Olympus SC50 microscope camera (Olympus Corporation, Japan).
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