We use essential cookies to operate our site. With your consent, we may also use non-essential cookies to improve your user experience and to analyze website traffic. Click "Accept" to accept cookies and go directly to the site, click "Reject" to reject all but cookies strictly necessary for the functioning of this site. You can reset your cookie settings at any time by visiting your Bioz "my account" page and selecting the "reset cookie preferences" link.

Accept Reject

All (14)
Olympus
Zeiss
Nikon
Leica Microsystems
Evident Corporation
Hamamatsu
KEYENCE
SciMedia
6 More...
 

About 41 products / 165 snippets / 9 images

80 / 100
Bioz Stars
Fluorescent macroscope
Olympus  
star_border
Techniques
 
Article Snippets
"Mice were placed under a fluorescent macroscope (microscope: MVX10, Olympus; light: PRIOR Lumen 1600-LED; camera: Flash 4.0 digital, Hamamatsu) in the lateral position."  (see more)
85 / 100
Bioz Stars
Fluorescent macroscope
Olympus  
star_border
Techniques
 
Article Snippets
"Imaging was performed using a fluorescent macroscope (Olympus, Lausanne, Switzerland)."  (see more)
5+  more images
Influence of calcein AM concentration and diluent on staining and CECs. ( A ) Comparison of calcein staining in four different conditions: 2 µM or 4 µM calcein diluted in PBS or Opti-MEM (Opt). ( A1 ) The DMEK graft was separated from the cornea and then cut into four parts. Each part was incubated in one of the four solutions differentiated by calcein concentration (2 or 4 µM) and diluent (PBS or Opt). After incubation for 45 min at RT, the four different parts of the same DMEK graft were spread on the same glass slide and observed simultaneously under the same field using a <t>fluorescence</t> <t>macroscope</t> at a magnification of ×0.8. ( A2 ) The fluorescence intensity of calcein in each of the four parts of the endothelium was measured and then compared. Five different DMEK grafts were used ( n = 5). The condition PBS-2 µM was considered as the control condition. The fluorescence intensity of the four parts of each graft was standardized with their respective control. The standardized fluorescence intensity was expressed as Mean +/− SD (Min, Max). One-sample t-test was utilized for statistical analysis, resulting in p = 0.0460 (*) for Opt-2 µM, p = 0.0111 (*) for PBS-4 µM, and p = 0.0096 (**) for Opt-4 µM. ( B ) Side-effects of using PBS as a diluent: alteration of cell junctions. ( B1 ) Calcein staining of endothelium was performed using dilutions in PBS or Opti-MEM under a microscope with a 10× objective. ( B2) Cell junctions were highlighted using IF under a microscope with a 40× objective. The arrowheads indicate dead zones, and the arrows show the cracks that formed between cell islands consisting of several to several dozen CECs.
CO-A
STAIN
COMP
INCU
FLUOR
Recombination efficiency of SMMHC-CreER T2 , SMArTTa-tetOCre, smMHC Cre/eGFP , and c-KitCreER T2 lines with ROSA26mT/mG . (A) Representative immunofluorescence maximal projections of a fixed SMMHC-CreER T2 -ROSA26mT/mG IALV stained for GFP and SMA to determine recombination efficiency. (B) Representative immunofluorescence maximal projections of a fixed SMArTTa-tetOCre-ROSA26mT/mG IALV stained with antibodies for GFP and SMA to determine recombination efficiency. (C) Representative immunofluorescence maximal projections of a smMHC Cre/eGFP IALV fixed and stained for GFP and SMA to determine recombination efficiency. (A–C) Comparisons of cell masks for SMA and GFP to highlight cells that were SMA-positive/GFP-negative and the merged maximal projection used to assess recombination efficiency. (D) Representative immunofluorescence maximal projections of a live and pressurized (2 cm H 2 O) c-KitCreER T2 -ROSA26mT/mG IALV imaged for GFP (recombined cells) and td-tomato (not recombined). Images were taken at 20× objective magnification. (E) Representative immunofluorescent images of the intestine muscle layer of a c-KitCreER T2 -ROSA26mT/mG induced with our tamoxifen injection protocol and acquired using a <t>fluorescence</t> <t>macroscope</t> revealed recombination of the c-Kit + interstitial cells of Cajal. RFP, red fluorescent protein (tdTomato); GFP, green fluorescent protein (EGFP).
IF
STAIN
INJECT
FLUOR
Expression pattern of the MtACT2 promoter in M. truncatula roots transformed with the MtACT2::DsRED-E5 fusion. A and B, MtACT2 promoter expression pattern in roots. Images were collected with the Leica stereo fluorescence <t>macroscope</t> using GFP (A) and DsRED (B) filter sets, respectively. C to E, Confocal fluorescence images of growing (C), growth terminating (D), and young mature (E) root hairs transformed with MtACT2::DsRED-E5. Nucleus is indicated by the arrowhead. Bars represent 10 μm.
EXP
TRNSF-A
FLUOR
The morphology of whole ethmoid turbinates was visible on bright field (BF) (a), and by DAPI staining (b). The OE was highlighted by immunostaining with Tuj-1 (c and e). The merge of Tuj-1 (green) and DAPI (blue) with or without BF (gray) indicated the olfactory boundary (d and f). The photos were acquired using a <t>fluorescence</t> <t>macroscope</t> with 1.6X objective for (a-d) and 5X objective for (e, f).
STAIN
IS
FLUOR
×
94 / 100
Bioz Stars
Fluorescent macroscope
Nikon  
star_border
Techniques
 
Article Snippets
".. with an acquisition rate of 0.5 Hz and a magnification of 25X using a fluorescent macroscope (Nikon AZ100)."  (see more)
94 / 100
Bioz Stars
Fluorescence macroscope
Olympus  
star_border
Techniques
 
Article Snippets
"Check fluorescence under a fluorescence macroscope (Olympus MVX10 Macroview Stereo Fluorescence Microscope or similar) to confirm correct HCR pattern."  (see more)
91 / 100
Bioz Stars
Fluorescence macroscope
Danaher / Leica Microsystems  
star_border
Techniques
 
Article Snippets
"For all experiments except spontaneous behavioral monitoring (detailed below), mice were head-fixed in a 1.5 inch diameter x 4 inch long polycarbonate tube ( ) and placed under a custom-built fluorescence macroscope consisting of back-to-back 50 mm objective lens .."  (see more)
92 / 100
Bioz Stars
Fluorescence macroscope
Nikon  
star_border
Techniques
 
Article Snippets
".. GFP+ cells in Tg(mbp:GFP-NTR) tadpoles were liveimaged using a fluorescence macroscope (Nikon Multizoom AZ100M)."  (see more)
80 / 100
Bioz Stars
Fluorescence macroscope
Thorlabs  
star_border
Techniques
 
Article Snippets
".. ketamine + 10mgkg−1 xylazine) mice were rigidly fixed under the fluorescence macroscope (self built, Thorlabs)."  (see more)
80 / 100
Bioz Stars
Fluorescence macroscope
Meiji Seika Pharma Co Ltd  
star_border
Techniques
 
Article Snippets
"We ppreciate Keyence Corporation, Osaka, Japan for providng fluorescence macroscope and also appreciate Meiji Seika aisha, Ltd. for providing talaporfin sodium. eferences [1] Stupp R, Mason .."  (see more)
90 / 100
Bioz Stars
Fluorescence macroscope
Zeiss  
star_border
Techniques
 
Article Snippets
"Photographs were taken using a fluorescence macroscope (Carl Zeiss, Thornwood, NY, USA), and the number of macrophages that adhered to the mouse .."  (see more)
92 / 100
Bioz Stars
Fluorescence macroscope
Zeiss  
star_border
Techniques
 
Article Snippets
"The remaining tissue was imaged using a fluorescence macroscope (Zeiss Axiozoom.v16) at 112× to reveal the GFP + interstitial cells of Cajal network."  (see more)
IF
STAIN
INJECT
FLUOR
90 / 100
Bioz Stars
Fluorescent macroscope
Zeiss  
star_border
Techniques
 
Article Snippets
".. slide in a drop of distilled water and observed using either a fluorescent macroscope (AxioZoom V16, Zeiss, Germany) or an inverted microscope (DMIRBE, Leica, Germany) with a CCD camera .."  (see more)
92 / 100
Bioz Stars
Fluorescence macroscope
SciMedia  
star_border
Techniques
 
Article Snippets
"The widefield calcium images were acquired through a fluorescence macroscope (Scimedia THT-FLSP) containing an sCMOS camera (PCO Edge 5.5) with a frame rate of .."  (see more)