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Carl lsm700 confocal microscope

Manufactured by Zeiss
Sourced in Germany

The Carl Zeiss LSM700 is a confocal microscope designed for high-resolution imaging. It utilizes a focused laser beam to scan the sample and generate detailed images. The microscope is capable of optical sectioning, allowing for the collection of three-dimensional data from the specimen.

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2 protocols using carl lsm700 confocal microscope

1

Confocal Imaging of Dual-Marker Transgenic Plants

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Confocal microscopy was performed on a Zeiss LSM700 and a Leica TCS SP8 confocal laser scanning microscope as previously reported (Kim et al., 2020 (link); Seo and Lee, 2021 (link)). Pictures were taken with either a 20× dry objective lens or a 63× water-immersion objective lens. For Z-scan imaging, the same position on the root and the same laser scanning area were chosen.
To image the ProTCSn::ntdTomato, ProDR5v2::n3GFP dual-marker line, seedlings were fixed in 4% paraformaldehyde and treated with ClearSee solution (Kurihara et al., 2015 (link)) for five days. The seedlings were then stained with 0.1% (v/v) calcofluor white 2MR (Sigma-Aldrich, USA) in ClearSee solution for 30 min and observed under a confocal microscope (Leica TCS SP8) with preset excitation/emission wavelengths of 488 nm/500-530 nm for GFP, 550 nm/580 nm for tdTomato and 350 nm/420 nm for calcofluor white 2MR. To visualize the GFP protein in other transgenic lines, seedlings were stained in a 1 μM propidium iodide (PI; Sigma-Aldrich, USA) solution for 2 min and observed under a Carl Zeiss LSM700 confocal microscope (Carl Zeiss, Germany) with the following excitation and detection windows: GFP 488 nm/500-530 nm; PI 555 nm/591-635 nm.
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2

Rat Aortic Smooth Muscle Cell Culture

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Rat SMCs (A7r5) were purchased (ATCC; CRL-1444; Manassas, VA) and grown in Dulbecco’s modified Eagle’s medium (DMEM) containing 0.2% Primocin and 10% fetal bovine serum (Atlanta Biologicals; Flowery Branch, GA) (referred to as “complete media”) up to passage 15. Cells were maintained at 37°C and 5% CO2 in a humidified incubator (ShelLab; Cornelius, OR) and serially passaged 1:2 in tissue culture-treated 75 cm2 flasks (USA Scientific; Ocala, FL). For trypsinization, conditioned media was aspirated, flasks were washed with 1× Dulbecco’s phosphate buffered saline (DPBS; Thermo Fisher Scientific; Waltham, MA) then cells were incubated for 5 min in 0.25% Trypsin/2.21 mM EDTA in Hank’s Balanced Salt Solution (HBSS) without sodium bicarbonate, calcium, or magnesium (Corning; Tewksbury, MA). Cell suspensions (supplemented with complete growth medium) were seeded in appropriate vessels: 60 mm petri dishes, six-well plates (tissue culture (TC)-treated; Corning), and ibidi 6.4 microchannel slides (glass or TC-treated bottoms; ibidi USA; Madison, WI) and allowed to attach/spread for specified times. Images were captured using a Leica DMI4000B inverted fluorescent microscope and CoolSnap HQ2 camera, EVOS FL Auto microscope (Life Technologies), or Carl Zeiss LSM 700 confocal microscope (Carl Zeiss, Germany).
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