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inverted fluorescence phase contrast microscope  (Carl Zeiss)


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    Carl Zeiss inverted fluorescence phase contrast microscope
    Inverted Fluorescence Phase Contrast Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 4854 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phase-fluorescence+microscope/Inverted+microscope+Axio+Observer+3/pmc12947217-159-26-30
    Average 99 stars, based on 4854 article reviews
    inverted fluorescence phase contrast microscope - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    other:

    Article Title: Differentiation, engraftment and functional effects of pre-treated mesenchymal stem cells in a rat myocardial infarct model
    Article Snippet: Differentiation, engraftment and functional effects of pre-treated mesenchymal stem cells in a rat myocardial infarct model Jihyun Yoon, Byoung Goo Min, Young-Hoon Kim, Wan Joo Shim, Young Moo Ro & Do-Sun Lim To cite this article: Jihyun Yoon, Byoung Goo Min, Young-Hoon Kim, Wan Joo Shim, Young Moo Ro & Do-Sun Lim (2005) Differentiation, engraftment and functional effects of pre-treated mesenchymal stem cells in a rat myocardial infarct model, Acta Cardiologica, 60:3, 277-284 To link to this article: https://doi.org/10.2143/AC.60.3.2005005



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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Journal: Current Research in Microbial Sciences

    Article Title: Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii

    doi: 10.1016/j.crmicr.2025.100543

    Figure Lengend Snippet: Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Article Snippet: All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Techniques: Fluorescence, Transformation Assay, Plasmid Preparation, In Vitro, Methylation, Modification, Microscopy