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1.4na oil immersion objective lens

Manufactured by Nikon

The 60× 1.4NA oil immersion objective lens is a high-performance microscope objective lens designed for use in laboratory applications. It provides a magnification of 60× and a numerical aperture of 1.4, which allows for the collection of a large amount of light and the creation of high-resolution images. This objective lens is intended for use with oil immersion techniques, which enhance the image quality by reducing the refractive index mismatch between the specimen and the lens.

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3 protocols using 1.4na oil immersion objective lens

1

Multimodal Live Cell Imaging Setup

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The fixed smFISH-IF samples were imaged on an automated inverted Nikon Ti-2 wide-field microscope equipped with a 60× 1.4NA oil immersion objective lens (Nikon), Spectra X LED light engine (Lumencor), and Orca 4.0 v2 scMOS camera (Hamamatsu).
The live cell imaging was conducted on a customized wide-field microscope built around a Nikon Ti-E stand. The microscope was equipped with three separate EMCCD cameras (Andor iXon Ultra 897) with ultra-flat 2 mm thick imaging splitting dichroic mirrors (T565LPXR-UF2, T640LPXR-UF2). Each of the cameras was equipped with band pass emission filter (ET525/50m, ET595/50m, and ET655lp). The light source of the microscope is an LU-n4 laser launch (Nikon) with four wavelengths: 405, 488, 561, and 640 nm. The excitation was done through H-TIRF with 100× 1.49NA oil immersion TIRF objective (Nikon). The excitation laser and fluorescence emission were separated by a quad band dichroic mirror (Chroma, ET-405/488/561/640 nm). The microscope was also equipped with an automated linear encoded XY-stage with Piezo-Z (Applied Scientific Instrumentation).
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2

Multicolor Live-Cell Microscopy Setup

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The fixed samples were imaged on an automated inverted Nikon Ti-2 wide-field microscope equipped with ×60 1.4NA oil immersion objective lens (Nikon), Spectra X LED light engine (Lumencor), and Orca 4.0 v2 scMOS camera (Hamamatsu). The live cell experiments were performed on a custom microscope built around Nikon Ti-E stand. The excitation was through HTIRF (Nikon) with an LU-n4 four laser unit (Nikon) with solid state lasers with wavelengths 405, 488, 561, and 640 nm. The main dichroic was a quad band dichroic mirror (Chroma, ET-405/488/561/640 nm laser quad band set for TIRF applications). The imaging was done through the ×100 1.49NA oil immersion objective (Nikon). To achieve simultaneous 3-color imaging, we used a TriCam light splitter into three separate EMCCD cameras (Andor iXon Ultra 897) with ultraflat 2 mm thick imaging splitting dichroic mirrors (T565LPXR-UF2, T640LPXR-UF2). A band pass emission filter was placed in front of each camera, respectively (ET525/50 m, ET595/50 m, and ET655lp). The microscope was also equipped with an automated XY-stage with extra fine lead-screw pitch of 0.635 mm and 10 nm linear encoder resolution and a Piezo-Z stage (Applied Scientific Instrumentation) for fast Z-acquisition. The whole microscope was under the control of Nikon Elements for automation.
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3

Live-cell and Electron Microscopy Imaging

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The fixed and living cells were observed under a TE2000 microscope (Nikon, Tokyo, Japan) equipped with a 100×/1.4 numerical aperture (NA) Plan-Apochromatic, a 60×/1.4 NA Plan-Apochromatic, or a 40×/1.3 NA Plan Fluor oil immersion objective lens (Nikon), a CSU-X1 confocal unit (Yokogawa, Tokyo, Japan), and an iXon3 electron-multiplier charge coupled device camera (Andor, Belfast, United Kingdom). Image acquisition was controlled by μManager software. Fluorescence recovery after photobleaching was performed using a C2 (Nikon) confocal microscope equipped with a 60×/1.4 NA oil immersion objective lens (Nikon). TEM was performed as previously described (Uehara et al., 2013 (link)).
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