014 to 0.018 mg/ml FITC-tank water for 10 to 15 min. The embryo was rinsed several times in fresh tank water and subsequently imaged with an imaging area and exposure time consistent with Figures 3, 4 and 5. No FITC dye was observed in the blastomere cells. (a) Weak autofluorescence was observed in the yolk. Scale bars for (a, b) represent 200 μm.<p><b>Copyright information:</b></p><p>Taken from "Laser surgery of zebrafish () embryos using femtosecond laser pulses: Optimal parameters for exogenous material delivery, and the laser's effect on short- and long-term development"</p><p>http://www.biomedcentral.com/1472-6750/8/7</p><p>BMC Biotechnology 2008;8():7-7.</p><p>Published online 29 Jan 2008</p><p>PMCID:PMC2270268.</p><p></p
(a) Cavitation bubble (Cb) was produced using an average laser power of 45 mW with a beam dwell time...
<p><b>A:</b> Representative optical images of zebrafish morphology after 72 hpf exposure to DFO, L1 ...
Dynamics of development can be followed by confocal time-lapse microscopy of live transgenic zebrafi...
(a, b) Embryo was porated for exogenous delivery using an average laser power of 45 mW with a beam d...
(d, e) High magnification SEM images of the blastomere-yolk interface of an 8-cell stage embryo. Sca...
<p>The GFP-expressing human ADSCs were transplanted into zebrafish embryos at 3.3–4.3 hpf after thei...
Owing to its optical clarity and rapid rate of development, the zebrafish embryo is an ideal model s...
<p>Human ADSCs expressed GFP were xenotransplanted into zebrafish embryos at 3.3–4.3 hpf after their...
The dataset contains a time-lapse (4D) volumetric fluorescence microscopy image sequence of a living...
Zebrafish embryos (ZFE) have increasingly gained in popularity as a model to perform safety screenin...
Owing to its optical clarity and rapid rate of development, the zebrafish embryo is an ideal model s...
Light sheet microscopy techniques, such as selective plane illumination microscopy (SPIM), are ideal...
<p>The extremity of the tail of a transgenic zebrafish embryo was cut at 3 dpf.</p> <p>At 16 hpa, t...
Zebrafish is now widely used in biomedical research as a model for human diseases, but the relevance...
A long-standing goal of biology is to map the behavior of all cells during vertebrate embryogenesis....
(a) Cavitation bubble (Cb) was produced using an average laser power of 45 mW with a beam dwell time...
<p><b>A:</b> Representative optical images of zebrafish morphology after 72 hpf exposure to DFO, L1 ...
Dynamics of development can be followed by confocal time-lapse microscopy of live transgenic zebrafi...
(a, b) Embryo was porated for exogenous delivery using an average laser power of 45 mW with a beam d...
(d, e) High magnification SEM images of the blastomere-yolk interface of an 8-cell stage embryo. Sca...
<p>The GFP-expressing human ADSCs were transplanted into zebrafish embryos at 3.3–4.3 hpf after thei...
Owing to its optical clarity and rapid rate of development, the zebrafish embryo is an ideal model s...
<p>Human ADSCs expressed GFP were xenotransplanted into zebrafish embryos at 3.3–4.3 hpf after their...
The dataset contains a time-lapse (4D) volumetric fluorescence microscopy image sequence of a living...
Zebrafish embryos (ZFE) have increasingly gained in popularity as a model to perform safety screenin...
Owing to its optical clarity and rapid rate of development, the zebrafish embryo is an ideal model s...
Light sheet microscopy techniques, such as selective plane illumination microscopy (SPIM), are ideal...
<p>The extremity of the tail of a transgenic zebrafish embryo was cut at 3 dpf.</p> <p>At 16 hpa, t...
Zebrafish is now widely used in biomedical research as a model for human diseases, but the relevance...
A long-standing goal of biology is to map the behavior of all cells during vertebrate embryogenesis....
(a) Cavitation bubble (Cb) was produced using an average laser power of 45 mW with a beam dwell time...
<p><b>A:</b> Representative optical images of zebrafish morphology after 72 hpf exposure to DFO, L1 ...
Dynamics of development can be followed by confocal time-lapse microscopy of live transgenic zebrafi...