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His2Av::eGFP is a fluorescent protein fusion construct that labels the histone variant H2Av in Drosophila. This construct allows for the visualization and tracking of H2Av dynamics within the cell nucleus.

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2 protocols using his2av egfp

1

Drosophila Embryo Imaging Protocol

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The Drosophila embryo used in this study (Fig. 2) expressed histone tagged with EGFP (w; His2Av::eGFP; Bloomington stock #23560). The embryos were collected by putting adult flies on a grape-juice agar plate for 45 min–1 h. After incubation at 25 °C for 1 h, the embryos were attached to a glass slide with double-sided tape. We use forceps to carefully roll an embryo on the tape until the embryo dechorionated. The Dechorionated embryos were embedded in 2% low-melting-temperature agarose in a Glass Bottom Dish (35 mm Dish with 20 mm Bottom Well, Cellvis). We put the Glass Bottom Dish on the microscope stage and scan the embryo along the z-axis 4 times with a 30 µm stride, then concatenate 4 reconstructed stacks to form the volume.
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2

Drosophila Imaging Toolkit Protocols

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The following fly strains were obtained from the Bloomington Drosophila Stock Center: nos-Gal4 (#7303), his2av::mRFP (#23651), his2av::eGFP (#24163), sti shRNA (#35392), sep2::GFP (#26257), sfGFP::sti (#81646), sqh::GFP (#57145), mRFP::anillin (#52220), shrub::GFP (#32559) and sfGFP::tum (#76264). We imaged Pavarotti (Pav) at endogenous levels with Pav::GFP22 (link) or with Pav::mCherry (this study). uasp-GFP-alix44 (link) flies were obtained from Kaisa Haglund (Oslo University Hospital) and uas-spas-eGFP51 (link) flies from Damien Brünner (University of Zurich). 20XUAS-mC3PA-GFP was provided by Pfeiffer et al.52 (link). We examined the behavior of microtubules with a GFP-tagged microtubule-binding protein Jupiter::GFP53 (link),54 (link) using the Jupiter::GFP FlyTrap line (CB05190).
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