axiovision 4.8.2 deconvolution algorithm Search Results


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The eggs, in different treatment, were observed using <t>stereomicroscope</t> as indicated in the figure. To remove the egg wax coating, 10-mg egg batches were treated with ~40–50 μL of heptane for ~15 min as described. A = unaltered egg clump, B = monolayer of treated eggs, C = clump of unaltered eggs floating on top of aqueous droplet (white arrowhead), D = de-waxed eggs submerged in the aqueous droplet (white asterisks sign). E = the hatching rate of eggs in different treatments, unaltered eggs (CTR), with heptane (W.H.), with heptane and hypochlorite (W.H. + Hyp.) and with heptane, hypochlorite and electroporated (W.H.+ Hyp.+elect). Magnification bars: A-D: 2000 μm, Insert: 500 μm. Statistical analysis was carried out using the ANOVA and posttest Tukey ( p <0.05), (Triplicate; n = 3).
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The eggs, in different treatment, were observed using <t>stereomicroscope</t> as indicated in the figure. To remove the egg wax coating, 10-mg egg batches were treated with ~40–50 μL of heptane for ~15 min as described. A = unaltered egg clump, B = monolayer of treated eggs, C = clump of unaltered eggs floating on top of aqueous droplet (white arrowhead), D = de-waxed eggs submerged in the aqueous droplet (white asterisks sign). E = the hatching rate of eggs in different treatments, unaltered eggs (CTR), with heptane (W.H.), with heptane and hypochlorite (W.H. + Hyp.) and with heptane, hypochlorite and electroporated (W.H.+ Hyp.+elect). Magnification bars: A-D: 2000 μm, Insert: 500 μm. Statistical analysis was carried out using the ANOVA and posttest Tukey ( p <0.05), (Triplicate; n = 3).
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The eggs, in different treatment, were observed using <t>stereomicroscope</t> as indicated in the figure. To remove the egg wax coating, 10-mg egg batches were treated with ~40–50 μL of heptane for ~15 min as described. A = unaltered egg clump, B = monolayer of treated eggs, C = clump of unaltered eggs floating on top of aqueous droplet (white arrowhead), D = de-waxed eggs submerged in the aqueous droplet (white asterisks sign). E = the hatching rate of eggs in different treatments, unaltered eggs (CTR), with heptane (W.H.), with heptane and hypochlorite (W.H. + Hyp.) and with heptane, hypochlorite and electroporated (W.H.+ Hyp.+elect). Magnification bars: A-D: 2000 μm, Insert: 500 μm. Statistical analysis was carried out using the ANOVA and posttest Tukey ( p <0.05), (Triplicate; n = 3).
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Image Search Results


The eggs, in different treatment, were observed using stereomicroscope as indicated in the figure. To remove the egg wax coating, 10-mg egg batches were treated with ~40–50 μL of heptane for ~15 min as described. A = unaltered egg clump, B = monolayer of treated eggs, C = clump of unaltered eggs floating on top of aqueous droplet (white arrowhead), D = de-waxed eggs submerged in the aqueous droplet (white asterisks sign). E = the hatching rate of eggs in different treatments, unaltered eggs (CTR), with heptane (W.H.), with heptane and hypochlorite (W.H. + Hyp.) and with heptane, hypochlorite and electroporated (W.H.+ Hyp.+elect). Magnification bars: A-D: 2000 μm, Insert: 500 μm. Statistical analysis was carried out using the ANOVA and posttest Tukey ( p <0.05), (Triplicate; n = 3).

Journal: PLoS ONE

Article Title: Non-Invasive Delivery of dsRNA into De-Waxed Tick Eggs by Electroporation

doi: 10.1371/journal.pone.0130008

Figure Lengend Snippet: The eggs, in different treatment, were observed using stereomicroscope as indicated in the figure. To remove the egg wax coating, 10-mg egg batches were treated with ~40–50 μL of heptane for ~15 min as described. A = unaltered egg clump, B = monolayer of treated eggs, C = clump of unaltered eggs floating on top of aqueous droplet (white arrowhead), D = de-waxed eggs submerged in the aqueous droplet (white asterisks sign). E = the hatching rate of eggs in different treatments, unaltered eggs (CTR), with heptane (W.H.), with heptane and hypochlorite (W.H. + Hyp.) and with heptane, hypochlorite and electroporated (W.H.+ Hyp.+elect). Magnification bars: A-D: 2000 μm, Insert: 500 μm. Statistical analysis was carried out using the ANOVA and posttest Tukey ( p <0.05), (Triplicate; n = 3).

Article Snippet: Subsequently, hatched and unhatched eggs were counted under a stereomicroscope (Carl Zeiss AxioVision 4.8.2 SP1).

Techniques: