stereo microscope camera Search Results


90
Motic Group stereo microscopes with mounted cameras
Stereo Microscopes With Mounted Cameras, supplied by Motic Group, 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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Point Grey Research Inc stereo microscope with cmos camera
Stereo Microscope With Cmos Camera, supplied by Point Grey Research Inc, 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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Carl Zeiss v20 stereo microscope with an axiocam mrc digital color camera
V20 Stereo Microscope With An Axiocam Mrc Digital Color Camera, supplied by Carl Zeiss, 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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Carl Zeiss stemi 508 stereo microscope with an axiocam 105 color camera
Stemi 508 Stereo Microscope With An Axiocam 105 Color Camera, supplied by Carl Zeiss, 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
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Euromex Microscopen high-resolution digital camera reflectance light microscope stereo blue euromex model
High Resolution Digital Camera Reflectance Light Microscope Stereo Blue Euromex Model, supplied by Euromex Microscopen, 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
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Carl Zeiss camera connected to a dissecting microscope stereo discovery v8
Camera Connected To A Dissecting Microscope Stereo Discovery V8, supplied by Carl Zeiss, 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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Carl Zeiss stereo dissecting microscope and dage-mti dc2000 ccd camera
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Stereo Dissecting Microscope And Dage Mti Dc2000 Ccd Camera, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/stereo dissecting microscope and dage-mti dc2000 ccd camera/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
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Teledyne Technologies stereo microscope equipped with a fixed-focus video camera lumenara 400
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Stereo Microscope Equipped With A Fixed Focus Video Camera Lumenara 400, supplied by Teledyne Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/stereo microscope equipped with a fixed-focus video camera lumenara 400/product/Teledyne Technologies
Average 90 stars, based on 1 article reviews
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90
Motic Group stereo zoom trinocular microscope with moticam 1080 attachable microscopy camera 2.0 mp
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Stereo Zoom Trinocular Microscope With Moticam 1080 Attachable Microscopy Camera 2.0 Mp, supplied by Motic Group, 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
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90
Carl Zeiss discovery v8 stereomicroscope equipped with an axiocam mrm camera
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Discovery V8 Stereomicroscope Equipped With An Axiocam Mrm Camera, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/discovery v8 stereomicroscope equipped with an axiocam mrm camera/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
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90
Carl Zeiss axiocam 105 stereo microscope camera
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Axiocam 105 Stereo Microscope Camera, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/axiocam 105 stereo microscope camera/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
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Carl Zeiss stereo optical microscope axiocamerc 5s microscope camera
Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo <t>dissecting</t> <t>microscope</t> and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.
Stereo Optical Microscope Axiocamerc 5s Microscope Camera, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/stereo optical microscope axiocamerc 5s microscope camera/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
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Image Search Results


Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo dissecting microscope and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.

Journal: The Journal of General Physiology

Article Title: Function of a STIM1 Homologue in C. elegans : Evidence that Store-operated Ca 2+ Entry Is Not Essential for Oscillatory Ca 2+ Signaling and ER Ca 2+ Homeostasis

doi: 10.1085/jgp.200609611

Figure Lengend Snippet: Induction of the intestinal unfolded protein response. (A) Fluorescent micrographs of control hsp-4 ∷GFP worms fed bacteria containing the empty feeding vector, control hsp-4 ∷GFP worms treated with tunicamycin, and hsp-4 ∷GFP worms fed either sca-1 or stim-1 dsRNA–producing bacteria. Worms were imaged using a stereo dissecting microscope and CCD camera (see Materials and methods). Images were obtained with identical camera settings. (B) Changes in whole worm fluorescence induced by tunicamycin (Tun), sca-1 RNAi, or stim-1 RNAi. Values are means ± SEM ( n = 275–732) and are plotted relative to fluorescence in control animals. *, P < 0.001 compared with control worms. (C) Effect of combined sca-1 and stim-1 RNAi on whole worm fluorescence. Values are means ± SEM ( n = 242–756) and are plotted relative to fluorescence in control animals. *, P < 0.0001 compared with sca-1 ( RNAi ) worms. Fluorescence levels in B and C were quantified using a COPAS BioSort and normalized to time-of-flight (i.e., GFP fluorescence/time-of-flight), which is a measure of worm size. Raw GFP fluorescence levels showed an identical pattern of change and statistical significance.

Article Snippet: Fluorescence and DIC micrographs were obtained using a Carl Zeiss MicroImaging Inc. M 2 BIO stereo dissecting microscope and DAGE-MTI DC2000 CCD camera or a Nikon TE2000 inverted microscope and a Micromax CCD-1300 camera (Princeton Instruments).

Techniques: Control, Bacteria, Plasmid Preparation, Microscopy, Fluorescence