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Plan apo 100 1.49 na objective

Manufactured by Nikon

The Plan-Apo 100× 1.49 NA objective is a high-performance objective lens designed for use in advanced microscopy applications. It features a 100× magnification and a numerical aperture of 1.49, providing excellent resolution and imaging capabilities. The objective is part of Nikon's Plan-Apo series, known for its flat field of view and accurate color reproduction.

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2 protocols using plan apo 100 1.49 na objective

1

Live-Cell Imaging of Axonal Transport

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For live imaging, cells were maintained in Hibernate E medium without phenol red (Brain-Bits). Images were acquired using a microscope (model Ti-E; Nikon) equipped with a spinning-disk confocal-head (model CSUW1, Yokogawa), and images were captured with an sCMOS camera (Zyla, Andor). KIF3AB and KIF3AC images were acquired with an Andor Dragonfly built on a Ti2 (Nikon) with a CFI Apo 60× 1.49 objective (Nikon) and captured with an sCMOS camera (Zyla 4.2+, Andor). The entire imaging stage and objectives were maintained at 37°C in a warmed enclosure (full lexan incubation ensemble; OkoLab). A Plan-Apo 100× 1.49 NA objective (Nikon) was used with 2 × 2 binning to acquire image streams. During image acquisition, z-axis movement was controlled by the Perfect Focus system on the Ti-E microscope (Nikon). Recordings were acquired at two frames per second. For further details, see Kaech et al.82 Axons were identified with anti-neurofascin antibody (NeuroMab, Cat #: 75–027) conjugated to CF405 (Mix-n-Stain CF405S Antibody Labeling Kit; Biotum, Cat#: 92231) in the imaging medium. Cells expressing constructs with HaloTag were treated with 50 nM Janelia Farm 549 dye18 (link) for 10 minutes and washed with conditioned medium for 10 minutes prior to imaging.
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2

Imaging Macrophage-T Cell Interactions

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RAW 264.7 mus musculus macrophages were seeded on glass coverslips at a concentration of 0.1 million cells per mL in DMEM and allowed to grow overnight. Cells were serum starved for 3 hours prior to imaging and maintained at 37.0 °C in 1× imaging buffer during imaging. Jurkat T cell membrane was labeled with DiO via incubation with 5 μM DiO at 37 °C for 2 minutes. Live cell images were acquired at a frame interval time of 2 seconds on a Nikon Eclipse-Ti epi-fluorescence microscope equipped with an Andor iXon3 EMCCD camera and a Nikon Plan Apo 100×/1.49 N.A. objective. Laser scanning confocal fluorescence imaging was done using a Nikon A1R-A1 confocal microscope system equipped with a Nikon 100× oilimmersed objective and a Hamamatsu C11440 camera.
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