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axio 257 imager a2 fluorescence microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axio 257 imager a2 fluorescence microscope
    Axio 257 Imager A2 Fluorescence Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 938 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/257+microscope/pm41633446-114-11-17?v=Carl+Zeiss
    Average 97 stars, based on 938 article reviews
    axio 257 imager a2 fluorescence microscope - by Bioz Stars, 2026-07
    97/100 stars

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    Yki knockdown accelerated midgut apoptosis. A, midgut morphology after dsYki or dsGFP injection as detailed in Fig. 3. LM, larval midgut; IM, imaginal midgut; M, muscle. The scale bar represents 50 μm. B, qRT-PCR showing the mRNA levels of IAP1 and Caspase3 after dsYki injection for 66 h in larval midgut in the above treatment. β-actin was used as the control. The asterisks denote significant differences (0.01 < p < 0.05, via Student's t test) based on three replicates. C, Yki knockdown increased Caspase3/7 activity in HaEpi cells. Caspase3/7 activity was detected in dsGFP and dsYki cells (dsRNA 2 μg/ml). Green fluorescence represents the Caspase3/7 activity, as assessed using a Caspase3/7 activity detection kit. Blue fluorescence indicates DAPI-stained nuclei. “Merge” is the superimposed images of the green and blue fluorescence. Fluorescence was observed using an Olympus <t>257</t> <t>BX51</t> fluorescence microscope. The scale bar represents 25 μm. D, statistical analyses of the ratio of Caspase3/7 activity cells in the total cells by ImageJ software. The values are expressed as the means ± S.D. (n = 3). The asterisks indicate significant difference calculated by Student's t test from three independent experiments.
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    JEOL energy dispersive 257 spectroscopy eds mappings
    Yki knockdown accelerated midgut apoptosis. A, midgut morphology after dsYki or dsGFP injection as detailed in Fig. 3. LM, larval midgut; IM, imaginal midgut; M, muscle. The scale bar represents 50 μm. B, qRT-PCR showing the mRNA levels of IAP1 and Caspase3 after dsYki injection for 66 h in larval midgut in the above treatment. β-actin was used as the control. The asterisks denote significant differences (0.01 < p < 0.05, via Student's t test) based on three replicates. C, Yki knockdown increased Caspase3/7 activity in HaEpi cells. Caspase3/7 activity was detected in dsGFP and dsYki cells (dsRNA 2 μg/ml). Green fluorescence represents the Caspase3/7 activity, as assessed using a Caspase3/7 activity detection kit. Blue fluorescence indicates DAPI-stained nuclei. “Merge” is the superimposed images of the green and blue fluorescence. Fluorescence was observed using an Olympus <t>257</t> <t>BX51</t> fluorescence microscope. The scale bar represents 25 μm. D, statistical analyses of the ratio of Caspase3/7 activity cells in the total cells by ImageJ software. The values are expressed as the means ± S.D. (n = 3). The asterisks indicate significant difference calculated by Student's t test from three independent experiments.
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    Image Search Results


    Yki knockdown accelerated midgut apoptosis. A, midgut morphology after dsYki or dsGFP injection as detailed in Fig. 3. LM, larval midgut; IM, imaginal midgut; M, muscle. The scale bar represents 50 μm. B, qRT-PCR showing the mRNA levels of IAP1 and Caspase3 after dsYki injection for 66 h in larval midgut in the above treatment. β-actin was used as the control. The asterisks denote significant differences (0.01 < p < 0.05, via Student's t test) based on three replicates. C, Yki knockdown increased Caspase3/7 activity in HaEpi cells. Caspase3/7 activity was detected in dsGFP and dsYki cells (dsRNA 2 μg/ml). Green fluorescence represents the Caspase3/7 activity, as assessed using a Caspase3/7 activity detection kit. Blue fluorescence indicates DAPI-stained nuclei. “Merge” is the superimposed images of the green and blue fluorescence. Fluorescence was observed using an Olympus 257 BX51 fluorescence microscope. The scale bar represents 25 μm. D, statistical analyses of the ratio of Caspase3/7 activity cells in the total cells by ImageJ software. The values are expressed as the means ± S.D. (n = 3). The asterisks indicate significant difference calculated by Student's t test from three independent experiments.

    Journal: The Journal of Biological Chemistry

    Article Title: The Steroid Hormone 20-Hydroxyecdysone Promotes the Cytoplasmic Localization of Yorkie to Suppress Cell Proliferation and Induce Apoptosis *

    doi: 10.1074/jbc.M116.719856

    Figure Lengend Snippet: Yki knockdown accelerated midgut apoptosis. A, midgut morphology after dsYki or dsGFP injection as detailed in Fig. 3. LM, larval midgut; IM, imaginal midgut; M, muscle. The scale bar represents 50 μm. B, qRT-PCR showing the mRNA levels of IAP1 and Caspase3 after dsYki injection for 66 h in larval midgut in the above treatment. β-actin was used as the control. The asterisks denote significant differences (0.01 < p < 0.05, via Student's t test) based on three replicates. C, Yki knockdown increased Caspase3/7 activity in HaEpi cells. Caspase3/7 activity was detected in dsGFP and dsYki cells (dsRNA 2 μg/ml). Green fluorescence represents the Caspase3/7 activity, as assessed using a Caspase3/7 activity detection kit. Blue fluorescence indicates DAPI-stained nuclei. “Merge” is the superimposed images of the green and blue fluorescence. Fluorescence was observed using an Olympus 257 BX51 fluorescence microscope. The scale bar represents 25 μm. D, statistical analyses of the ratio of Caspase3/7 activity cells in the total cells by ImageJ software. The values are expressed as the means ± S.D. (n = 3). The asterisks indicate significant difference calculated by Student's t test from three independent experiments.

    Article Snippet: Fluorescence was observed using an Olympus 257 BX51 fluorescence microscope.

    Techniques: Injection, Quantitative RT-PCR, Activity Assay, Fluorescence, Staining, Microscopy, Software