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Plan apochromat 40 1.4 objective

Manufactured by Zeiss
Sourced in Germany

The Plan-Apochromat 40x/1.4 objective is a high-performance microscope objective designed by Zeiss. It features a numerical aperture of 1.4, which allows for high-resolution imaging. The objective is classified as a Plan-Apochromat, indicating it is designed to provide a flat and color-corrected image field.

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4 protocols using plan apochromat 40 1.4 objective

1

Zeiss Confocal Imaging of C. elegans Migration

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Representative images were acquired with a Zeiss LSM700 confocal microscope using a Plan-Apochromat 40×/1.4 objective. Worms were immobilized using 1.5% 1-phenoxy-2-propanol (TCI America, Portland, OR) in M9 buffer and mounted on 5% agar slides. 3D reconstructions were done using Zeiss Zen software. A Zeiss Axio Imager two microscope equipped with Chroma HQ filters was used to score AMsh migration defects and take images to measure Migration Index. Experiments were conducted in triplicates consisting of at least 50 day one adult animals each.
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2

Quantification of GABA Neuron Synapses

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Representative images were acquired with a Zeiss LSM700 confocal microscope using a Plan-Apochromat 40×/1.4 objective. Worms were immobilized using 1.5% 1-phenoxy-2-propanol (TCI America, Portland, OR) in M9 buffer and mounted on 5% agar slides. 3D reconstructions were done using Zeiss Zen software. Images of GABA neuron synapses show the dorsal cord at the middle part of animals. A Zeiss Axio Imager 2 microscope equipped with Chroma HQ filters was used to score AMsh migration defects and take images to measure Migration Index. For GABA neuron synapse number quantification, a Zeiss Axio Imager 2 microscope equipped with Chroma HQ filters was used to quantify the total number of SNB-1::GFP puncta at the dorsal cord. Each condition represented 3 experiments of at least 50 Day 1 adult animals each unless otherwise noted.
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3

Quantification of GABA Neuron Synapses

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Representative images were acquired with a Zeiss LSM700 confocal microscope using a Plan-Apochromat 40×/1.4 objective. Worms were immobilized using 1.5% 1-phenoxy-2-propanol (TCI America, Portland, OR) in M9 buffer and mounted on 5% agar slides. 3D reconstructions were done using Zeiss Zen software. Images of GABA neuron synapses show the dorsal cord at the middle part of animals. A Zeiss Axio Imager 2 microscope equipped with Chroma HQ filters was used to score AMsh migration defects and take images to measure Migration Index. For GABA neuron synapse number quantification, a Zeiss Axio Imager 2 microscope equipped with Chroma HQ filters was used to quantify the total number of SNB-1::GFP puncta at the dorsal cord. Each condition represented 3 experiments of at least 50 Day 1 adult animals each unless otherwise noted.
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4

Muscle Imaging with Confocal Microscopy

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Muscle slices were mounted on two cover glasses and imaged with an inverted confocal fluorescence microscope (LSM710, Zeiss, Oberkochen, Germany) equipped with the Fluar 10×/0.5 objective (dry; working distance, 2.0 mm), Plan-Apochromat 20×/0.8 objective (dry; working distance, 0.55 mm), Plan-Apochromat 40×/1.4 objective (oil; working distance, 0.13 mm), and alpha Plan-Apochromat ×63/1.46 objective (oil; working distance, 0.10 mm).
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