axiozoom microscope apotome structural illumination module Search Results


96
Carl Zeiss axiozoom v16 zoom microscope
Axiozoom V16 Zoom Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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94
Carl Zeiss fluorescence screening zoom microscope
Fluorescence Screening Zoom Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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96
Carl Zeiss zoom stereomicroscope
The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom <t>stereomicroscope.</t> i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm
Zoom Stereomicroscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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97
Carl Zeiss stereo zoom microscope
The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom <t>stereomicroscope.</t> i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm
Stereo Zoom Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiozoom+microscope+apotome+structural+illumination+module/Zoom+microscope+Axio+Zoom%2EV16/pm32320079-72-6-10
Average 97 stars, based on 1 article reviews
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96
Carl Zeiss microscope zeiss axiozoom v16
The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom <t>stereomicroscope.</t> i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm
Microscope Zeiss Axiozoom V16, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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96
Carl Zeiss fluorescence stereomicroscope
The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom <t>stereomicroscope.</t> i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm
Fluorescence Stereomicroscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiozoom+microscope+apotome+structural+illumination+module/Fluorescence+stereomicroscope+SteREO+Discovery%2EV8+with+stand+N/pmc04898200-58-7-9
Average 96 stars, based on 1 article reviews
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99
Nikon ti eclipse inverted microscope
A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 <t>microscope,</t> M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).
Ti Eclipse Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
ti eclipse inverted microscope - by Bioz Stars, 2026-10
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96
Carl Zeiss axiozoom v16 microscope
A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 <t>microscope,</t> M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).
Axiozoom V16 Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiozoom+microscope+apotome+structural+illumination+module/Objective+PlanNeoFluar+Z+2%2E3x%2F0%2E57+FWD/bio_rxiv__2023__02__11__528145-170-9-8
Average 96 stars, based on 1 article reviews
axiozoom v16 microscope - by Bioz Stars, 2026-10
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90
KEYENCE fluorescence microscope keyence bz-x700
A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 <t>microscope,</t> M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).
Fluorescence Microscope Keyence Bz X700, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
fluorescence microscope keyence bz-x700 - by Bioz Stars, 2026-10
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97
Carl Zeiss stereomicroscope
A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 <t>microscope,</t> M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).
Stereomicroscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiozoom+microscope+apotome+structural+illumination+module/Stereomicroscope+SteREO+Discovery%2EV8+with+stand+300/pm25681352-89-16-18
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Image Search Results


The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom stereomicroscope. i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm

Journal: Horticulture Research

Article Title: Sclareol and linalyl acetate are produced by glandular trichomes through the MEP pathway

doi: 10.1038/s41438-021-00640-w

Figure Lengend Snippet: The chemical composition of the epidermal surface of clary sage calyces was analyzed through laser desorption–ionization followed by FT-ICR mass spectrometry (LDI–FT-ICR). a Representative mass spectrum of the surface of a clary sage calyx. Spatial distribution of [L+K] + ions ( b ), [L+L+K] + ions ( d ), [S+K] + ions ( c ) [S+S+K] + ions ( e ) and at the surface of the calyx sample. f Overlay of [L+K] + and [L+L+K] + ions. g Overlay of [S+K] + and [S+S+K] + ions. h Top view of a clary sage calyx sample observed with a zoom stereomicroscope. i Overlay of [L+K] + , [L+L+K] + , [S+K] + , and [S+S+K] + ions. Blue arrowheads indicate short capitate glandular trichomes, circles indicate large capitate glandular trichomes, dashed circles indicate peltate glandular trichomes. L linalyl acetate, S sclareol, Scale bar: 100 µm

Article Snippet: Optical images showing top views of calyx samples were taken using a zoom stereomicroscope (AxioZoom V16, Zeiss).

Techniques: Mass Spectrometry

A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 microscope, M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).

Journal: bioRxiv

Article Title: EPP1 is an ancestral component of the plant Common Symbiosis Pathway

doi: 10.1101/2025.09.30.679610

Figure Lengend Snippet: A-C Percentage root length colonization of Medicago truncatula EPP1 RNAi lines ( A ), Petunia hybrida ( B ) and Brachypodium distachyon ( C ) mutant lines. Stars indicate significant differences between wild-type and mutants (Welch t-test). F Colonization quantification of Marchantia paleacea epp1 mutants with distance between the thallus notch and colonized area (top) and percentage of colonized thalli (bottom). Bar represent median value. Number of observed thalli is indicated. Letters indicate statistical differences (ANOVA, posthoc Tukey). Each bar corresponds to an independent transformed line. NM = Non-Mycorrhized. DEG Schematic representations of the epp1 mutations in P . hybrida ( D ), B . distachyon ( E ) and M. paleacea ( G ). Scale bar = 100bp. IJ Representative pictures of the phenotypes of P. hybrida ( I ) and M. paleacea ( J ) epp1 and their respective wild types. R. irregularis is visualized with blue ink ( I ) or with WGA-Alexa Fluor 488 ( J ). P. hybrida images were taken using a Zeiss Axiozoom V16 microscope, M. paleacea using a Nikon Ti Eclipse. Scale bar = 0.25 mm ( I ), 0.5mm ( J ).

Article Snippet: Images were taken using a Zeiss Axiozoom V16 microscope or a Nikon Ti Eclipse inverted microscope equipped with DS Ri2 camera.

Techniques: Mutagenesis, Transformation Assay, Microscopy