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Axiovison

Manufactured by Zeiss
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Sourced in Germany

AxioVision is a software package designed for image acquisition, processing, and analysis. It is compatible with a range of Zeiss microscopy systems and digital cameras, enabling users to capture, manage, and analyze high-quality images.

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Lab products found in correlation

Deadend fluorometric tunel system kit, by Promega (2 mentions) Axioplan 2 microscope, by Zeiss (2 mentions)

Spelling variants of this product

Axiovison 4.8 (20 citations) Axiovison software (9 citations) Axiovison A2 (3 citations) Axiovison 2.0 software (2 citations) Axiovison software v4.2 (2 citations) Zeiss AxioVison 4.7.1 extended focus module (2 citations) ZEN and AxioVison (2 citations)

5 protocols using axiovison

1

TUNEL Assay of MDA-MB-231 Xenograft Tumors

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TUNEL assay of MDA-MB-231 xenograft tumor tissues was performed with DeadEnd™ Fluorometric TUNEL System Kit (Cat# G3250, Promega, Madison, WI) following the manufacturer’s protocol. Briefly, the frozen mouse tumor slides were washed with ice-cold PBS. Cells were fixed, permeabilized, and labeled with biotinylated nucleotide mix by terminal deoxynucleotidyl transferase (rTdT) reaction. Fragmented DNA was detected by streptavidin-conjugated fluorescence using Zeiss Axioplan 2 microscope. The AxioVison (Carl Zeiss) was used for data analysis.
Du Y., Yamaguchi H., Wei Y., Hsu J.L., Wang H.L., Hsu Y.H., Lin W.C., Yu W.H., Leonard P.G., Lee GR I.V., Chen M.K., Nakai K., Hsu M.C., Chen C.T., Sun Y., Wu Y., Chang W.C., Huang W.C., Liu C.L., Chang Y.C., Chen C.H., Park M., Jones P., Hortobagyi G.N, & Hung M.C. (2016). Blocking c-Met-mediated PARP1 phosphorylation enhances anti-tumor effects of PARP inhibitors. Nature medicine, 22(2), 194-201.
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2

Endothelial Cell Response to Biomaterials

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All measurements are presented as mean ± standard deviation. The
t-test and chi-square test were used for comparison between the two groups. Intimal thickening and endothelial cell proliferation were measured using the AxioVison (Carl Zeiss Oberkochen Germany). A risk rate of less than 5% (
p < 0.05) was considered statistically significant.
Wakako A., Sadato A., Oeda M., Higashiguchi S., Hayakawa M., Oshima M, & Hirose Y. (2023). Development of a Model for Plaque Induction in Rat Carotid Arteries. Asian Journal of Neurosurgery, 18(3), 499-507.
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3

Immunohistochemistry of Xenograft Tumors

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Frozen MDA-MB-231 xenograft tumor slides were washed with ice-cold PBS. Cells were fixed, permeabilized, and incubated with Ki67 and γ-H2AX antibodies and fluorescent-labeled secondary antibodies. Immunostained cells were examined using Zeiss Axioplan 2 microscope (Carl Zeiss, Thornwood, NY) with a 20X objective. The AxioVison (Carl Zeiss) was used for data analysis.
Du Y., Yamaguchi H., Wei Y., Hsu J.L., Wang H.L., Hsu Y.H., Lin W.C., Yu W.H., Leonard P.G., Lee GR I.V., Chen M.K., Nakai K., Hsu M.C., Chen C.T., Sun Y., Wu Y., Chang W.C., Huang W.C., Liu C.L., Chang Y.C., Chen C.H., Park M., Jones P., Hortobagyi G.N, & Hung M.C. (2016). Blocking c-Met-mediated PARP1 phosphorylation enhances anti-tumor effects of PARP inhibitors. Nature medicine, 22(2), 194-201.
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4

Immunohistochemistry of Xenograft Tumors

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Frozen MDA-MB-231 xenograft tumor slides were washed with ice-cold PBS. Cells were fixed, permeabilized, and incubated with Ki67 and γ-H2AX antibodies and fluorescent-labeled secondary antibodies. Immunostained cells were examined using Zeiss Axioplan 2 microscope (Carl Zeiss, Thornwood, NY) with a 20X objective. The AxioVison (Carl Zeiss) was used for data analysis.
Du Y., Yamaguchi H., Wei Y., Hsu J.L., Wang H.L., Hsu Y.H., Lin W.C., Yu W.H., Leonard P.G., Lee GR I.V., Chen M.K., Nakai K., Hsu M.C., Chen C.T., Sun Y., Wu Y., Chang W.C., Huang W.C., Liu C.L., Chang Y.C., Chen C.H., Park M., Jones P., Hortobagyi G.N, & Hung M.C. (2016). Blocking c-Met-mediated PARP1 phosphorylation enhances anti-tumor effects of PARP inhibitors. Nature medicine, 22(2), 194-201.
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5

TUNEL Assay of MDA-MB-231 Xenograft Tumors

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TUNEL assay of MDA-MB-231 xenograft tumor tissues was performed with DeadEnd™ Fluorometric TUNEL System Kit (Cat# G3250, Promega, Madison, WI) following the manufacturer’s protocol. Briefly, the frozen mouse tumor slides were washed with ice-cold PBS. Cells were fixed, permeabilized, and labeled with biotinylated nucleotide mix by terminal deoxynucleotidyl transferase (rTdT) reaction. Fragmented DNA was detected by streptavidin-conjugated fluorescence using Zeiss Axioplan 2 microscope. The AxioVison (Carl Zeiss) was used for data analysis.
Du Y., Yamaguchi H., Wei Y., Hsu J.L., Wang H.L., Hsu Y.H., Lin W.C., Yu W.H., Leonard P.G., Lee GR I.V., Chen M.K., Nakai K., Hsu M.C., Chen C.T., Sun Y., Wu Y., Chang W.C., Huang W.C., Liu C.L., Chang Y.C., Chen C.H., Park M., Jones P., Hortobagyi G.N, & Hung M.C. (2016). Blocking c-Met-mediated PARP1 phosphorylation enhances anti-tumor effects of PARP inhibitors. Nature medicine, 22(2), 194-201.
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