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celltracker red cmtpx dye  (Thermo Fisher)


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    Thermo Fisher celltracker red cmtpx dye
    Celltracker Red Cmtpx Dye, supplied by Thermo Fisher, 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/celltracker%E2%84%A2+red+cmtpx/celltracker+green/pm40659786-680-16-26
    Average 90 stars, based on 1 article reviews
    celltracker red cmtpx dye - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Staining:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Irradiation:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Incubation:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Cell Culture:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Labeling:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Multiple Displacement Amplification:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Suspension:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Fluorescence:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Expressing:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).

    Marker:

    Article Title: GEI-17-Mediated SUMOylation of GDI-1 Regulates Apoptotic Cell Clearance
    Article Snippet: Jurkat cells were stained with 1 μM CellTrackerTM Red CMTPX (Invitrogen, E34552) for 30 min, and then irradiated with 150 J UV, followed by incubation at 37 °C 5% CO 2 for 3 h to generate apoptosis.

    Article Title: Method of preparing an artificial tooth primordium in vitro and artificial tooth primordium derived therefrom
    Article Snippet: Afterwards primary human keratinocytes tracked with CellTrackerTM Red CMTPX (Molecular Probes®) were added as single cell suspension of epithelial cells in a ratio of 1:4 related to the initial cell number used for mesenchymal condensation and the resulting mixture was cultured under non-adherent conditions.

    Article Title: Uptake Mechanism of ApoE-Modified Nanoparticles on Brain Capillary Endothelial Cells as a Blood-Brain Barrier Model
    Article Snippet: After this incubation the cells were washed twice with serum-free medium and the cytosol was stained with CellTrackerTM Red CMTPX (Invitrogen, Karlsruhe, Germany) as described in the manufacturer instructions manual.

    Article Title: Sema4D-plexin-B1 signaling in recruiting dental stem cells for vascular stabilization on a microfluidic platform.
    Article Snippet: HUVECs were labeled with CellTrackerTM Red CMTPX (Invitrogen) and SHED were labeled with CellTrackerTM Green CMFDA (Invitrogen).

    Article Title: Epithelial to Mesenchymal Transition in the Endometrium Mediated by HOXA10 drives Embryo Implantation
    Article Snippet: Briefly, mycoplasma free trophoblast cells (HTR8/SV-neo cells ATCC-CRL-3271) cultured in DMEM-F12 and 10% FBS were seeded in low attachment plates (PerkimElmer) and 24h later the spheroids were labeled with CellTrackerTM Red CMTPX (Invitrogen).

    Article Title: L1CAM is required for early dissemination of fallopian tube carcinoma precursors to the ovary
    Article Snippet: Cells not expressing a fluorescent marker were resuspended in serum free media and 1 × 10 5 cells/ovary were incubated with a red fluorescent dye (CellTrackerTM Red CMTPX, life technologies) for 30 min at 37 °C before washing 3 times with PBS.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: MDA-MB-231, HUVEC, HDFa, or THP-cells were stained either with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) or CellTraceTM CSFE (5 μM, C34554, Invitrogen) in OptiMEM.

    Article Title: Tumoral hypoxic extracellular vesicles create a protective microenvironment for triple-negative breast cancer
    Article Snippet: THP-1 cells were pre-stained with CellTrackerTM Red CMTPX (5 μM, C34552, Invitrogen) and transferred to the reservoir containing EVh (10 9 particles/ml) or vehicle (PBS).



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    Azenta sparse celltracker red cmtpx labeled cells
    (A) Experimental design for assessing S. aureus replication dynamics in MG63 osteoblastic cells. (B-K) MG63 cells, seeded at sparse density and labeled with <t>CellTracker</t> Red CMTPX (red), were infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. (B-G) Representative confocal images and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time. Images show single osteoblastic cells infected by: exclusively non-replicative S. aureus (B, C ), or at least one S. aureus transitioning from quiescence to slow replication (D, E) or fast replication leading to host cell lysis (F, G) (scale bar = 10 µm). (H) Hourly quantification of infected cells based on intracellular S. aureus replication dynamics (RD) across the 24-hour infection period. (I) Initiation and duration of the fast replicative phases. (J) Hourly quantification of infected cells experiencing either an ongoing or an ended fast replicative phase. (K) Global quantification of infected cells based on intracellular S. aureus replication dynamics over an infection period of 24 hours (ENR: Exclusively non-replicative; SR: slow replicative; FR: fast replicative). (H-K) Results were presented as mean ± SD (H, J, K) or median and quartiles (I) , representing 36 individual values (H, J, K) from 12 independent experiments ( H , K : N = 1005 infected cells, I , J : N = 474 infected cells). Mann-Whitney test: **** p < 0.0001.
    Sparse Celltracker Red Cmtpx Labeled Cells, supplied by Azenta, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/celltracker%E2%84%A2+red+cmtpx/cells+celltracker+cmtpx+labeled+red+sparse/pmc12478902-282-13-21
    Average 86 stars, based on 1 article reviews
    sparse celltracker red cmtpx labeled cells - by Bioz Stars, 2026-09
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    celltracker red cmtpx dye  (Thermo Fisher)
    90
    Thermo Fisher celltracker red cmtpx dye
    (A) Experimental design for assessing S. aureus replication dynamics in MG63 osteoblastic cells. (B-K) MG63 cells, seeded at sparse density and labeled with <t>CellTracker</t> Red CMTPX (red), were infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. (B-G) Representative confocal images and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time. Images show single osteoblastic cells infected by: exclusively non-replicative S. aureus (B, C ), or at least one S. aureus transitioning from quiescence to slow replication (D, E) or fast replication leading to host cell lysis (F, G) (scale bar = 10 µm). (H) Hourly quantification of infected cells based on intracellular S. aureus replication dynamics (RD) across the 24-hour infection period. (I) Initiation and duration of the fast replicative phases. (J) Hourly quantification of infected cells experiencing either an ongoing or an ended fast replicative phase. (K) Global quantification of infected cells based on intracellular S. aureus replication dynamics over an infection period of 24 hours (ENR: Exclusively non-replicative; SR: slow replicative; FR: fast replicative). (H-K) Results were presented as mean ± SD (H, J, K) or median and quartiles (I) , representing 36 individual values (H, J, K) from 12 independent experiments ( H , K : N = 1005 infected cells, I , J : N = 474 infected cells). Mann-Whitney test: **** p < 0.0001.
    Celltracker Red Cmtpx Dye, supplied by Thermo Fisher, 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/celltracker%E2%84%A2+red+cmtpx/celltracker+green/pm40659786-680-16-26
    Average 90 stars, based on 1 article reviews
    celltracker red cmtpx dye - by Bioz Stars, 2026-09
    90/100 stars
    		  Buy from Supplier
    celltracker red cmtpx  (Thermo Fisher)
    90
    Thermo Fisher celltracker red cmtpx
    (A) Experimental design for assessing S. aureus replication dynamics in MG63 osteoblastic cells. (B-K) MG63 cells, seeded at sparse density and labeled with <t>CellTracker</t> Red CMTPX (red), were infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. (B-G) Representative confocal images and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time. Images show single osteoblastic cells infected by: exclusively non-replicative S. aureus (B, C ), or at least one S. aureus transitioning from quiescence to slow replication (D, E) or fast replication leading to host cell lysis (F, G) (scale bar = 10 µm). (H) Hourly quantification of infected cells based on intracellular S. aureus replication dynamics (RD) across the 24-hour infection period. (I) Initiation and duration of the fast replicative phases. (J) Hourly quantification of infected cells experiencing either an ongoing or an ended fast replicative phase. (K) Global quantification of infected cells based on intracellular S. aureus replication dynamics over an infection period of 24 hours (ENR: Exclusively non-replicative; SR: slow replicative; FR: fast replicative). (H-K) Results were presented as mean ± SD (H, J, K) or median and quartiles (I) , representing 36 individual values (H, J, K) from 12 independent experiments ( H , K : N = 1005 infected cells, I , J : N = 474 infected cells). Mann-Whitney test: **** p < 0.0001.
    Celltracker Red Cmtpx, supplied by Thermo Fisher, 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/celltracker%E2%84%A2+red+cmtpx/celltracker+green/pmc10694756__mmc2-418-115-118
    Average 90 stars, based on 1 article reviews
    celltracker red cmtpx - by Bioz Stars, 2026-09
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    (A) Experimental design for assessing S. aureus replication dynamics in MG63 osteoblastic cells. (B-K) MG63 cells, seeded at sparse density and labeled with CellTracker Red CMTPX (red), were infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. (B-G) Representative confocal images and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time. Images show single osteoblastic cells infected by: exclusively non-replicative S. aureus (B, C ), or at least one S. aureus transitioning from quiescence to slow replication (D, E) or fast replication leading to host cell lysis (F, G) (scale bar = 10 µm). (H) Hourly quantification of infected cells based on intracellular S. aureus replication dynamics (RD) across the 24-hour infection period. (I) Initiation and duration of the fast replicative phases. (J) Hourly quantification of infected cells experiencing either an ongoing or an ended fast replicative phase. (K) Global quantification of infected cells based on intracellular S. aureus replication dynamics over an infection period of 24 hours (ENR: Exclusively non-replicative; SR: slow replicative; FR: fast replicative). (H-K) Results were presented as mean ± SD (H, J, K) or median and quartiles (I) , representing 36 individual values (H, J, K) from 12 independent experiments ( H , K : N = 1005 infected cells, I , J : N = 474 infected cells). Mann-Whitney test: **** p < 0.0001.

    Journal: PLOS Pathogens

    Article Title: Monitoring intracellular replication dynamics unveils high proportion of non-replicating antibiotic-tolerant Staphylococcus aureus inside osteoblasts

    doi: 10.1371/journal.ppat.1013525

    Figure Lengend Snippet: (A) Experimental design for assessing S. aureus replication dynamics in MG63 osteoblastic cells. (B-K) MG63 cells, seeded at sparse density and labeled with CellTracker Red CMTPX (red), were infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. (B-G) Representative confocal images and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time. Images show single osteoblastic cells infected by: exclusively non-replicative S. aureus (B, C ), or at least one S. aureus transitioning from quiescence to slow replication (D, E) or fast replication leading to host cell lysis (F, G) (scale bar = 10 µm). (H) Hourly quantification of infected cells based on intracellular S. aureus replication dynamics (RD) across the 24-hour infection period. (I) Initiation and duration of the fast replicative phases. (J) Hourly quantification of infected cells experiencing either an ongoing or an ended fast replicative phase. (K) Global quantification of infected cells based on intracellular S. aureus replication dynamics over an infection period of 24 hours (ENR: Exclusively non-replicative; SR: slow replicative; FR: fast replicative). (H-K) Results were presented as mean ± SD (H, J, K) or median and quartiles (I) , representing 36 individual values (H, J, K) from 12 independent experiments ( H , K : N = 1005 infected cells, I , J : N = 474 infected cells). Mann-Whitney test: **** p < 0.0001.

    Article Snippet: Infection was performed at MOI 8 (or 2 or 4 where indicated) using sparse CellTracker Red CMTPX-labeled cells in 24-well plates (4TITUDE, 4TI-0241) or 96-well plates (Greiner bio-one, 655090), as described above.

    Techniques: Labeling, Infection, Expressing, Incubation, Imaging, Confocal Microscopy, Fluorescence, Lysis, MANN-WHITNEY

    MG63 cells labeled (B , D) or not ( A , C , E ) with CellTracker Red CMTPX (red) were seeded at sparse (B , D) or confluent (A , C , E) density and infected and treated as previously described in (BJI035: rifampicin resistant). (A) At 2 hpi propidium iodide (PI) was added at 2 µg/mL. At 24 hpi PI fluorescence intensity was measured with a plate reader. PI fluorescence intensity is normalized to uninfected cells in untreated and rifampicin-treated conditions. (B) Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. Quantification of the S. aureus SH1000 population size per cell over time represented by the total green (GFP) pixel count normalized per cell. (C, E) Intracellular S. aureus SH1000 were collected at 1 hpi and 24 hpi, and the total number of S. aureus forming colonies on agar plate was investigated (C) as well as their area distribution frequency at 24 hpi (E) and the small colony variants rates (F) . (D) At 6 hpi, rifampicin treatment was either withdrawn by washing or maintained, and incubation continued. Time-lapse imaging was conducted over 18 hours post-withdrawal with hourly acquisitions using automated confocal microscopy. Quantification of infected cells based on intracellular S. aureus replication dynamics (RD). Results were presented either as single value and mean ± SD from 3 independent experiments (B, E) or as mean ± SD representing 9 individual values from 3 independent experiments (A , D : N = 165 infected cells, F) or 12 individual values from 4 independent experiments (C) . One-way ANOVA with Dunnett’s correction for multiple post hoc comparisons with the control (A) and Mann-Whitney test (C , D, F) : *p < 0.05, **p < 0.01, ****p < 0.0001.

    Journal: PLOS Pathogens

    Article Title: Monitoring intracellular replication dynamics unveils high proportion of non-replicating antibiotic-tolerant Staphylococcus aureus inside osteoblasts

    doi: 10.1371/journal.ppat.1013525

    Figure Lengend Snippet: MG63 cells labeled (B , D) or not ( A , C , E ) with CellTracker Red CMTPX (red) were seeded at sparse (B , D) or confluent (A , C , E) density and infected and treated as previously described in (BJI035: rifampicin resistant). (A) At 2 hpi propidium iodide (PI) was added at 2 µg/mL. At 24 hpi PI fluorescence intensity was measured with a plate reader. PI fluorescence intensity is normalized to uninfected cells in untreated and rifampicin-treated conditions. (B) Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy. Quantification of the S. aureus SH1000 population size per cell over time represented by the total green (GFP) pixel count normalized per cell. (C, E) Intracellular S. aureus SH1000 were collected at 1 hpi and 24 hpi, and the total number of S. aureus forming colonies on agar plate was investigated (C) as well as their area distribution frequency at 24 hpi (E) and the small colony variants rates (F) . (D) At 6 hpi, rifampicin treatment was either withdrawn by washing or maintained, and incubation continued. Time-lapse imaging was conducted over 18 hours post-withdrawal with hourly acquisitions using automated confocal microscopy. Quantification of infected cells based on intracellular S. aureus replication dynamics (RD). Results were presented either as single value and mean ± SD from 3 independent experiments (B, E) or as mean ± SD representing 9 individual values from 3 independent experiments (A , D : N = 165 infected cells, F) or 12 individual values from 4 independent experiments (C) . One-way ANOVA with Dunnett’s correction for multiple post hoc comparisons with the control (A) and Mann-Whitney test (C , D, F) : *p < 0.05, **p < 0.01, ****p < 0.0001.

    Article Snippet: Infection was performed at MOI 8 (or 2 or 4 where indicated) using sparse CellTracker Red CMTPX-labeled cells in 24-well plates (4TITUDE, 4TI-0241) or 96-well plates (Greiner bio-one, 655090), as described above.

    Techniques: Labeling, Infection, Fluorescence, Imaging, Confocal Microscopy, Incubation, Control, MANN-WHITNEY

    MG63 cells labeled (A , C - G) or not (B) with CellTracker Red CMTPX (red) were seeded at sparse density and infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Concomitantly, cells were treated with rifampicin at 6 µg/mL and/or ciprofloxacin at 2, 5, or 10 µg/mL or left untreated. Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy (A , C - G) or intracellular S. aureus were collected at 1 hpi and 24 hpi, and total number of S. aureus forming colonies on agar plate was investigated (B) . (A , C) Quantification of infected cells based on intracellular S. aureus replication dynamics (RD) over an infection period of 24 hours. (B) Total number of intracellular S. aureus SH1000 forming colonies on plates. (D) Quantification of the S. aureus population size per cell over time represented by the total green (GFP) pixel count normalized per cell. Represent 1 experiment of 3 for easier readability. (E , F) Representative confocal images (E) and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time (F) . Images show a single osteoblastic cell infected by S. aureus SH1000 experiencing an arrested fast replicative phase under ciprofloxacin treatment at 2 µg/mL (scale bar = 10 µm). (G) Quantification of the proportion of arrested fast replicative phases relative to the total fast replicative events measured. Results were presented either as mean ± SD representing 9 individual values from 3 independent experiments ( A : N = 1288, C : N = 745, G : N = 258 infected cells) or as 12 individual values from 4 independent experiments (B) . One-way ANOVA with Dunnett’s correction for multiple post hoc comparisons with the control (A , C , G) or Two-way ANOVA test with Sidak’s correction for multiple comparisons post hoc test ( B ; p < 0.05: treatment, p < 0.0001: time): * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Journal: PLOS Pathogens

    Article Title: Monitoring intracellular replication dynamics unveils high proportion of non-replicating antibiotic-tolerant Staphylococcus aureus inside osteoblasts

    doi: 10.1371/journal.ppat.1013525

    Figure Lengend Snippet: MG63 cells labeled (A , C - G) or not (B) with CellTracker Red CMTPX (red) were seeded at sparse density and infected at MOI 8 with S. aureus SH1000 expressing GFP (green) pre-labeled by eFluor-450 (blue). Following 2 hours of co-incubation, lysostaphin at 10 µg/mL was added to eliminate extracellular S. aureus . Concomitantly, cells were treated with rifampicin at 6 µg/mL and/or ciprofloxacin at 2, 5, or 10 µg/mL or left untreated. Time-lapse imaging was conducted over 24 hours with hourly acquisitions using automated confocal microscopy (A , C - G) or intracellular S. aureus were collected at 1 hpi and 24 hpi, and total number of S. aureus forming colonies on agar plate was investigated (B) . (A , C) Quantification of infected cells based on intracellular S. aureus replication dynamics (RD) over an infection period of 24 hours. (B) Total number of intracellular S. aureus SH1000 forming colonies on plates. (D) Quantification of the S. aureus population size per cell over time represented by the total green (GFP) pixel count normalized per cell. Represent 1 experiment of 3 for easier readability. (E , F) Representative confocal images (E) and corresponding quantification of green (GFP) and blue (eFluor-450) fluorescence intensities over time (F) . Images show a single osteoblastic cell infected by S. aureus SH1000 experiencing an arrested fast replicative phase under ciprofloxacin treatment at 2 µg/mL (scale bar = 10 µm). (G) Quantification of the proportion of arrested fast replicative phases relative to the total fast replicative events measured. Results were presented either as mean ± SD representing 9 individual values from 3 independent experiments ( A : N = 1288, C : N = 745, G : N = 258 infected cells) or as 12 individual values from 4 independent experiments (B) . One-way ANOVA with Dunnett’s correction for multiple post hoc comparisons with the control (A , C , G) or Two-way ANOVA test with Sidak’s correction for multiple comparisons post hoc test ( B ; p < 0.05: treatment, p < 0.0001: time): * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Article Snippet: Infection was performed at MOI 8 (or 2 or 4 where indicated) using sparse CellTracker Red CMTPX-labeled cells in 24-well plates (4TITUDE, 4TI-0241) or 96-well plates (Greiner bio-one, 655090), as described above.

    Techniques: Labeling, Infection, Expressing, Incubation, Imaging, Confocal Microscopy, Fluorescence, Control