multichannel fluorescence microscopy imager z2 (Carl Zeiss)
Carl Zeiss is a verified supplier 
Carl Zeiss manufactures this product 
90
Structured Review
Carl Zeiss
multichannel fluorescence microscopy imager z2
Multichannel Fluorescence Microscopy Imager Z2, 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/product/multichannel+fluorescence+microscopy/microscope+z2/pmc12066426-53-34-39
Average 90 stars, based on 1 article reviews
Multichannel Fluorescence Microscopy Imager Z2, 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/product/multichannel+fluorescence+microscopy/microscope+z2/pmc12066426-53-34-39
Average 90 stars, based on 1 article reviews
multichannel fluorescence microscopy imager z2 - by Bioz Stars,
2026-11
90/100 stars
Images
1) Product Images from "Fluorescein-distribution in confocal laser endomicroscopy allows for discrimination between primary brain tumours and metastases"
Article Title: Fluorescein-distribution in confocal laser endomicroscopy allows for discrimination between primary brain tumours and metastases
Journal: Frontiers in Surgery
doi: 10.3389/fsurg.2025.1567711
Figure Legend Snippet: Time-dependent fluorescence intensity and representative microscopy images. (a) Mean fluorescence intensity in Ln229 cells as a function of incubation time. Error bars indicate the 95% confidence interval. (b–g) Fluorescent images of a Ln229 cell monolayer stained with SF (b,d) , PI (c,f) and Hoechst (d,g) for 40 min. Exposure time was adjusted for each picture individually. Dynamic display range was set to the minimum/maximum non-zero value for the green and DAPI channels; for the red channel the maximum pixel value was set to the camera's maximum pixel value of 16,384. White bar ∼50 μm. (a–d) Incubation of living cells, (e,f) Incubation of fixed cells.
Techniques Used: Fluorescence, Microscopy, Incubation, Staining
Figure Legend Snippet: Comparison of fluorescence intensity between different cell lines after SF stain. (a) Differential fluorescence intensity per cell line. Dotted pattern: glioma cell lines, striped pattern: adenocarcinoma cell lines. Error bars indicate the 95% confidence interval. *indicates a significance level of 0.05. For cell lines Ln18, T98G, and Ln229 differences to all of the adenocarcinoma were significant at the 0.05 level. (b–i) Representative fluorescence microscopy images of the stained cell lines: (b) Ln18, (c) T98G, (d) Ln229, (e) U87MG, (f) MCF7, (g) SW48, (h) MDA, and (i) OV-MZ-6. Scale bars: 25 µm.
Techniques Used: Comparison, Fluorescence, Staining, Microscopy
Figure Legend Snippet: (A) resected metastasis after intravenous application of SF in conventional fluorescence microscopy. Scale bar: 50 µm. (B) H&E staining of the same metastasis as a comparison. Scale bar: 50 µm.
Techniques Used: Fluorescence, Microscopy, Staining, Comparison
Related Articles
Fluorescence:Article Title: Differential expression of tension-sensitive HOX genes in fibroblasts is associated with different scar types Article Snippet: To label nuclei, 4’,6-diamidino-2-phenylindole (DAPI, 1:50000 dilution, Molecular Probes) was treated in the cells for 3min. .. Cells were then imaged using Article Title: Physicochemically Tuned Myofibroblasts for Wound Healing Strategy Article Snippet: During the staining step, we treat α-smooth muscle actin (α-SMA) antibody (Abcam) (with 1:100 dilution) for 12 hours, Alex Flour 488-fluorescence antibody (Invitrogen) (with 1:200 dilution) for 6 hours, Alex Fluor 568-phalloidin (Invitrogen) (with 1:50 dilution) for 20 min, and 4’,6-diamidino-2-phenylindole (DAPI, Molecular Probe) (with 1:50000 dilution) for 3 min. .. The Article Title: Fibrous Matrix Architecture-Dependent Activation of Fibroblasts with a Cancer-Associated Fibroblast-like Phenotype. Article Snippet: Cancer-associated fibroblasts (CAFs) are one of the most prevalent cell types within the tumor microenvironment (TME).. While several physicochemical cues from the TME, including growth factors, cytokines, and ECM specificity, have been identified as essential factors for CAF activation, the precise mechanism of how the ECM architecture regulates CAF initiation remains elusive.. Using a gelatin-based electrospun fiber mesh, we examined the effect of matrix fiber density on CAF activation induced by MCF-7 conditioned media (CM). Article Title: Tension-sensitive HOX gene expression in fibroblasts for differential scar formation. Article Snippet: To label nuclei, 4’,6-diamidino-2-phenylindole (DAPI, 1:50000 dilution, Molecular Probes) was treated in the cells for 3 min. .. Cells were then imaged using Article Title: Intradermal injection of low dose human regulatory T cells inhibits skin inflammation in a humanized mouse model Article Snippet: The secondary antibody for K16 was AF488-conjugated donkey anti-mouse IgG (ThermoFisher); for hBD2 AF546-conjugated donkey anti-goat (ThermoFisher), and for CD3 AF647-conjugated donkey anti-rabbit (ThermoFisher). .. Sections were photographed using a microscope (AxioImager M2; Zeiss, Sliedrecht, the Netherlands) and a high resolution color camera for bright field microscopy (AxioCam 105 color, Zeiss) and a high resolution b/w camera for Microscopy:Article Title: Differential expression of tension-sensitive HOX genes in fibroblasts is associated with different scar types Article Snippet: To label nuclei, 4’,6-diamidino-2-phenylindole (DAPI, 1:50000 dilution, Molecular Probes) was treated in the cells for 3min. .. Cells were then imaged using Article Title: Physicochemically Tuned Myofibroblasts for Wound Healing Strategy Article Snippet: During the staining step, we treat α-smooth muscle actin (α-SMA) antibody (Abcam) (with 1:100 dilution) for 12 hours, Alex Flour 488-fluorescence antibody (Invitrogen) (with 1:200 dilution) for 6 hours, Alex Fluor 568-phalloidin (Invitrogen) (with 1:50 dilution) for 20 min, and 4’,6-diamidino-2-phenylindole (DAPI, Molecular Probe) (with 1:50000 dilution) for 3 min. .. The Article Title: Fibrous Matrix Architecture-Dependent Activation of Fibroblasts with a Cancer-Associated Fibroblast-like Phenotype. Article Snippet: Cancer-associated fibroblasts (CAFs) are one of the most prevalent cell types within the tumor microenvironment (TME).. While several physicochemical cues from the TME, including growth factors, cytokines, and ECM specificity, have been identified as essential factors for CAF activation, the precise mechanism of how the ECM architecture regulates CAF initiation remains elusive.. Using a gelatin-based electrospun fiber mesh, we examined the effect of matrix fiber density on CAF activation induced by MCF-7 conditioned media (CM). Article Title: Tension-sensitive HOX gene expression in fibroblasts for differential scar formation. Article Snippet: To label nuclei, 4’,6-diamidino-2-phenylindole (DAPI, 1:50000 dilution, Molecular Probes) was treated in the cells for 3 min. .. Cells were then imaged using Article Title: Intradermal injection of low dose human regulatory T cells inhibits skin inflammation in a humanized mouse model Article Snippet: The secondary antibody for K16 was AF488-conjugated donkey anti-mouse IgG (ThermoFisher); for hBD2 AF546-conjugated donkey anti-goat (ThermoFisher), and for CD3 AF647-conjugated donkey anti-rabbit (ThermoFisher). .. Sections were photographed using a microscope (AxioImager M2; Zeiss, Sliedrecht, the Netherlands) and a high resolution color camera for bright field microscopy (AxioCam 105 color, Zeiss) and a high resolution b/w camera for Immunofluorescence:Article Title: Physicochemically Tuned Myofibroblasts for Wound Healing Strategy Article Snippet: During the staining step, we treat α-smooth muscle actin (α-SMA) antibody (Abcam) (with 1:100 dilution) for 12 hours, Alex Flour 488-fluorescence antibody (Invitrogen) (with 1:200 dilution) for 6 hours, Alex Fluor 568-phalloidin (Invitrogen) (with 1:50 dilution) for 20 min, and 4’,6-diamidino-2-phenylindole (DAPI, Molecular Probe) (with 1:50000 dilution) for 3 min. .. The Staining:Article Title: Fibrous Matrix Architecture-Dependent Activation of Fibroblasts with a Cancer-Associated Fibroblast-like Phenotype. Article Snippet: Cancer-associated fibroblasts (CAFs) are one of the most prevalent cell types within the tumor microenvironment (TME).. While several physicochemical cues from the TME, including growth factors, cytokines, and ECM specificity, have been identified as essential factors for CAF activation, the precise mechanism of how the ECM architecture regulates CAF initiation remains elusive.. Using a gelatin-based electrospun fiber mesh, we examined the effect of matrix fiber density on CAF activation induced by MCF-7 conditioned media (CM). |