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S plan apochromat objectives

Manufactured by Olympus
Sourced in Japan

The S Plan Apochromat objectives from Olympus are high-performance optical lenses designed for microscopy applications. They are engineered to provide superior image quality and color correction across a wide range of wavelengths, ensuring accurate and detailed observations.

Automatically generated - may contain errors

3 protocols using s plan apochromat objectives

1

Quantifying Hippocampal Neurogenesis in Blast Mice

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A one‐in‐twelve series of coronal sections was immunolabeled for doublecortin, and images of the dentate gyrus were captured and doublecortin+ neurons counted throughout the rostrocaudal extent of dorsal hippocampus in repeat blast mice and the matched shams using a 40x objective on an Olympus BH2 series light microscope with S Plan Apochromat objectives, an achromatic condenser (Olympus Corporation) and SPOT idea camera (Diagnostic instruments, Inc.) running on SPOT Advanced software (Version 4.6). Doublecortin+ cells with obvious cell bodies were counted, regardless of the presence of stained dendritic processes, through the entirety of dorsal hippocampus, using the same boundary between dorsal and ventral hippocampus described above for volume measurements.
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2

Optic Nerve Axon Quantification

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For optic nerve axon quantification, low and high magnification images were captured using an Olympus BH2 series light microscope with S Plan Apochromat objectives, an achromatic condenser (Olympus Corporation, Tokyo, Japan) and SPOT idea ™ camera (Diagnostic instruments, Inc., Sterling Heights, MI) running on SPOT Advanced software (Version 4.6). A low power image of each optic nerve was captured using a 20x objective to measure its cross sectional area and to divide the nerve into quadrants. A high power image of a subfield within each quadrant was then captured near its mid-point so that the images did not overlap or include the edges of the nerve, using a 100x oil immersion objective. The image of each subfield was overlain with a 4×6 grid of twenty-four 100 microns2 counting boxes, and 2 boxes per row per grid randomly chosen for count axons. For each counting box, axons falling on the north and east lines of the grid were included, but axons on the south and west lines of the grid were not. The total number of axons counted was divided by the total box area counted to calculate an axon density for each quadrant, axon densities for the 4 quadrants were averaged, and the total number of axons estimated by multiplying the optic nerve cross sectional area by the axon density.
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3

Quantifying Neurogenesis in Dorsal Hippocampus

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A one-in-twelve series of coronal sections was immunolabeled for doublecortin and images of the dentate gyrus were captured and doublecortin+ neurons counted throughout the rostrocaudal extent of dorsal hippocampus in repeat blast mice and the matched shams using a 40x objective on an Olympus BH2 series light microscope with S Plan Apochromat objectives, an achromatic condenser (Olympus Corporation, Tokyo, Japan) and SPOT idea camera (Diagnostic instruments, Inc., Sterling Heights, MI) running on SPOT Advanced software (Version 4.6). Doublecortin+ cells with obvious cell bodies were counted, regardless of the presence of stained dendritic processes, through the entirety of dorsal hippocampus, using the same boundary between dorsal and ventral hippocampus described above for volume measurements.
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