tem and sem image of nanoparticles Search Results


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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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eds  (JEOL)
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JEOL eds
Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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JEOL jem 2200fs transmission electron microscope
Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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JEOL jsm 7800f
Confocal <t>microscopy</t> demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.
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Image Search Results


Confocal microscopy demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.

Journal: Nanoscale Advances

Article Title: Magnetic nanoparticle mediated-gene delivery for simpler and more effective transformation of Pichia pastoris

doi: 10.1039/d1na00079a

Figure Lengend Snippet: Confocal microscopy demonstration of cellular uptake of MNPs in yeast treated with TRITC-labelled MNPs. (A) 2D confocal microscope images. The scale bar is 5 μm. (B) Quantitative analysis of confocal images. (C) Z -Stack images from yeast treated with TRITC-labelled MNPs.

Article Snippet: The size and morphology of the Fe 3 O 4 @PEI MNPs were obtained via transmission and scanning electron microscopy (TEM, Hitachi HighTech HT7700, and SEM, Carl Zeiss), respectively.

Techniques: Confocal Microscopy, Microscopy

Integration of GFP coding sequence into the P. pastoris genome. Agarose gel electrophoresis image of PCR products performed with (A) the gene specific primers (GFP forward and GFP reverse; 731 bp) and (B) the vector specific primers (pGAP forward and 3′AOX1; 963 bp). Also, magneto-transformation was performed with pGKB plasmid (276 bp). (C) gDNA and gene specific or/gene and vector specific primers (pGAP forward and GFP reverse; 767 bp). M: marker and V: vector, pGKB-GFP. (D) The images of GFP produced colonies after magneto-transformation by confocal microscopy. The scale bar is 10 μm. (E) The fluorescence intensity result was calculated from confocal images.

Journal: Nanoscale Advances

Article Title: Magnetic nanoparticle mediated-gene delivery for simpler and more effective transformation of Pichia pastoris

doi: 10.1039/d1na00079a

Figure Lengend Snippet: Integration of GFP coding sequence into the P. pastoris genome. Agarose gel electrophoresis image of PCR products performed with (A) the gene specific primers (GFP forward and GFP reverse; 731 bp) and (B) the vector specific primers (pGAP forward and 3′AOX1; 963 bp). Also, magneto-transformation was performed with pGKB plasmid (276 bp). (C) gDNA and gene specific or/gene and vector specific primers (pGAP forward and GFP reverse; 767 bp). M: marker and V: vector, pGKB-GFP. (D) The images of GFP produced colonies after magneto-transformation by confocal microscopy. The scale bar is 10 μm. (E) The fluorescence intensity result was calculated from confocal images.

Article Snippet: The size and morphology of the Fe 3 O 4 @PEI MNPs were obtained via transmission and scanning electron microscopy (TEM, Hitachi HighTech HT7700, and SEM, Carl Zeiss), respectively.

Techniques: Sequencing, Agarose Gel Electrophoresis, Plasmid Preparation, Transformation Assay, Marker, Produced, Confocal Microscopy, Fluorescence