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Princeton instruments micromax

Manufactured by Teledyne

The Princeton Instruments MicroMAX is a compact and versatile scientific imaging camera designed for a wide range of microscopy and spectroscopy applications. It features a high-sensitivity, low-noise CCD sensor and advanced electronics for high-quality image capture. The MicroMAX offers flexible connectivity options and can be easily integrated into various experimental setups.

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2 protocols using princeton instruments micromax

1

Fluorescent Imaging of Oocyte Dynamics

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An inverted microscope (Axiovert 100; Carl Zeiss) equipped with an interline cooled CCD camera (Princeton Instruments MicroMAX; Roper Scientific) was used for the recording of epifluorescence images of oocytes incubated in M2 medium at 37 °C. GFP-tagged Geminin was imaged using a filter set comprised of an excitation filter with a band pass of 450–490 nm, a dichroic mirror 510 nm and a band pass 505–520 nm emission filter. A DAPI (4,6-diamidino-2-phenylindole) filter set was used for imaging Hoechst 33342 (excitation filter: 340–380 nm, dichroic mirror: 400–420 nm, emission filter: 435–485 nm). Oocytes were imaged every 15 min to minimize photobleaching and photodamage. Data were collected and analysed using MetaMorph and Meta-Fluor software 6.1 (Molecular Devices).
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2

Oocyte Microinjection and Fluorescence Imaging

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All microinjections of GV stage oocytes were performed in M2 medium on the stage of an inverted microscope (DM IRB; Leica). In brief, fabricated micropipettes were inserted into cells using the negative capacitance overcompensation facility on an electrophysiological amplifier (World Precision Instruments), whereas cells were immobilized with a holding pipette (Hunter Scientific). A precise injection volume (2–5% of the total egg volume) was achieved using a pressure regulator (Pneumatic PicoPump; World Precision Instruments). Epifluorescence images of oocytes incubated in M2 medium at 37°C were recorded using an objective (20×, 0.75 NA) on an inverted microscope (Axiovert 100; Carl Zeiss) equipped with an interline cooled charge-coupled device camera (Princeton Instruments MicroMAX; Roper Scientific). GFP-tagged securin and geminin were imaged using an FITC filter set at band pass 450–490 nm for excitation, dichroic mirror 510 nm, and band pass 520 nm for emission. Oocytes were imaged every 10 min to minimize photobleaching and photodamage. MetaMorph and MetaFluor software 6.1 (Molecular Devices) were used for image capture and data analysis.
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