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Yeasen Biotechnology fluorescent celltracker green cmfda
Fluorescent Celltracker Green Cmfda, supplied by Yeasen Biotechnology, 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+green+cmfda/celltracker+cmfda+green/pm41803885-140-7-12
Average 86 stars, based on 1 article reviews
fluorescent celltracker green cmfda - by Bioz Stars, 2026-09
86/100 stars

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Related Articles

Labeling:

Article Title: piR-1170 drives brain metastasis and immune evasion via WTAP-mediated m6A methylation reprogramming in triple-negative breast cancer.
Article Snippet: .. Then, the tops of the monolayers were seeded with cancer cells labeled with CellTracker Green CMFDA (Yeasen Biotech, Shanghai, China). ..

Article Title: piR-1170 drives brain metastasis and immune evasion via WTAP-mediated m6A methylation reprogramming in triple-negative breast cancer
Article Snippet: .. Then, the tops of the monolayers were seeded with cancer cells labeled with CellTracker Green CMFDA (Yeasen Biotech, Shanghai, China). ..

Article Title: CircADAMTS12 Inhibits the Anti-Tumor Activity of Microglia to Enable Metastatic Colonization in the Brain
Article Snippet: 28 Microglia promote anti-tumor immunity and suppress breast-to-brain metastasis 29 (B2BM), which is a lethal complication in breast cancer patients without effective 30 therapeutic options.. Unraveling the molecular mechanism by which B2BM cancer 31 cells evade microglial-mediated anti-tumor immunity in the brain could reveal 32 potential treatment strategies.. Here, we showed that gain of expression of the circular 33 RNA circADAMTS12 in cancer cells supported breast cancer metastatic colonization 34 in the brain by suppressing the anti-tumor activity of microglia.

RNA Extraction:

Article Title: Turning aging cells into a live vaccine: engineered senescent cancer cells with adjuvant celecoxib for immunotherapy
Article Snippet: PC-98T, cholesterol, and DSPE-MPEG2000 were obtained from AVT Pharmaceutical Tech Co., Ltd. (Shanghai, China). .. Total RNA extraction reagent, SYBR green master mix, and CellTracker green CMFDA (5-chloromethyl fluorescein diacetate) were purchased from Yeasen Biotechnology Co., Ltd. (Shanghai, China). .. Murine granulocyte-macrophage colony-stimulating factor (GM-CSF) and murine interleukin 4 (IL-4) were purchased from Novus Biologicals (Centennial, USA).

SYBR Green Assay:

Article Title: Turning aging cells into a live vaccine: engineered senescent cancer cells with adjuvant celecoxib for immunotherapy
Article Snippet: PC-98T, cholesterol, and DSPE-MPEG2000 were obtained from AVT Pharmaceutical Tech Co., Ltd. (Shanghai, China). .. Total RNA extraction reagent, SYBR green master mix, and CellTracker green CMFDA (5-chloromethyl fluorescein diacetate) were purchased from Yeasen Biotechnology Co., Ltd. (Shanghai, China). .. Murine granulocyte-macrophage colony-stimulating factor (GM-CSF) and murine interleukin 4 (IL-4) were purchased from Novus Biologicals (Centennial, USA).

Staining:


Concentration Assay:


Incubation:




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Yeasen Biotechnology celltracker green cmfda
Upregulated piR-1170 facilitates TNBC brain metastasis. A Schematic of the brain metastasis model establishment in BALB/c nude mice. B-C In vivo bioluminescence imaging ( B ) and corresponding fluorescence intensities ( C ) at 10 min, 14 days, 21 days and 28 days post-implantation ( n = 6 per group). D Representative images of HE staining in brain metastatic lesion formed by anta-NC and anta-1170 cells. E Tissues from the brain-metastatic lesion were used for IF staining to observe cancer cell-astrocyte interaction. Tumor cells, astrocyte cells and nuclei were stained with pan-CK (green), GFAP (red) or DAPI (blue), respectively. F Representative images of blood vessel densities in brain metastases formed by anta-NC and anta-1170 cells. Vascular endothelial cells and nuclei were stained with CD31 (red) or DAPI (blue), respectively. G-H In vivo bioluminescence imaging ( G ) and corresponding fluorescence intensities ( H ) at 0–72 h post-intracardiac injection ( n = 6 per group). I Tumor cell extravasation analysis at 48 h post-injection, showing <t>CMFDA-labeled</t> tumor cells (green), CD31 + vasculature (red), and DAPI + nuclei (blue), with quantitative extravasation data. J Quantitative analysis of tumor cell adhesion to astrocyte monolayers after alteration of piR-1170 in vitro. K Quantitative assessment of tumor cell adhesion to human brain microvascular endothelial cells (HBMECs) after alteration of piR-1170 in vitro. The error bars represent the SDs of triplicate experiments
Celltracker Green Cmfda, supplied by Yeasen Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
celltracker green cmfda - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier

Image Search Results


Upregulated piR-1170 facilitates TNBC brain metastasis. A Schematic of the brain metastasis model establishment in BALB/c nude mice. B-C In vivo bioluminescence imaging ( B ) and corresponding fluorescence intensities ( C ) at 10 min, 14 days, 21 days and 28 days post-implantation ( n = 6 per group). D Representative images of HE staining in brain metastatic lesion formed by anta-NC and anta-1170 cells. E Tissues from the brain-metastatic lesion were used for IF staining to observe cancer cell-astrocyte interaction. Tumor cells, astrocyte cells and nuclei were stained with pan-CK (green), GFAP (red) or DAPI (blue), respectively. F Representative images of blood vessel densities in brain metastases formed by anta-NC and anta-1170 cells. Vascular endothelial cells and nuclei were stained with CD31 (red) or DAPI (blue), respectively. G-H In vivo bioluminescence imaging ( G ) and corresponding fluorescence intensities ( H ) at 0–72 h post-intracardiac injection ( n = 6 per group). I Tumor cell extravasation analysis at 48 h post-injection, showing CMFDA-labeled tumor cells (green), CD31 + vasculature (red), and DAPI + nuclei (blue), with quantitative extravasation data. J Quantitative analysis of tumor cell adhesion to astrocyte monolayers after alteration of piR-1170 in vitro. K Quantitative assessment of tumor cell adhesion to human brain microvascular endothelial cells (HBMECs) after alteration of piR-1170 in vitro. The error bars represent the SDs of triplicate experiments

Journal: Molecular Cancer

Article Title: piR-1170 drives brain metastasis and immune evasion via WTAP-mediated m6A methylation reprogramming in triple-negative breast cancer

doi: 10.1186/s12943-026-02568-y

Figure Lengend Snippet: Upregulated piR-1170 facilitates TNBC brain metastasis. A Schematic of the brain metastasis model establishment in BALB/c nude mice. B-C In vivo bioluminescence imaging ( B ) and corresponding fluorescence intensities ( C ) at 10 min, 14 days, 21 days and 28 days post-implantation ( n = 6 per group). D Representative images of HE staining in brain metastatic lesion formed by anta-NC and anta-1170 cells. E Tissues from the brain-metastatic lesion were used for IF staining to observe cancer cell-astrocyte interaction. Tumor cells, astrocyte cells and nuclei were stained with pan-CK (green), GFAP (red) or DAPI (blue), respectively. F Representative images of blood vessel densities in brain metastases formed by anta-NC and anta-1170 cells. Vascular endothelial cells and nuclei were stained with CD31 (red) or DAPI (blue), respectively. G-H In vivo bioluminescence imaging ( G ) and corresponding fluorescence intensities ( H ) at 0–72 h post-intracardiac injection ( n = 6 per group). I Tumor cell extravasation analysis at 48 h post-injection, showing CMFDA-labeled tumor cells (green), CD31 + vasculature (red), and DAPI + nuclei (blue), with quantitative extravasation data. J Quantitative analysis of tumor cell adhesion to astrocyte monolayers after alteration of piR-1170 in vitro. K Quantitative assessment of tumor cell adhesion to human brain microvascular endothelial cells (HBMECs) after alteration of piR-1170 in vitro. The error bars represent the SDs of triplicate experiments

Article Snippet: Then, the tops of the monolayers were seeded with cancer cells labeled with CellTracker Green CMFDA (Yeasen Biotech, Shanghai, China).

Techniques: In Vivo, Imaging, Fluorescence, Staining, Injection, Labeling, In Vitro

piR-1170 confers survival advantage in TNBC brain metastasis. A Schematic of intracranial injection-based brain metastasis model. B-C In vivo bioluminescence imaging ( B ) and corresponding fluorescence intensities ( C ) at 1 day, 3 days, 7 days and 11 days post-implantation ( n = 6 per group). D Representative HE staining images of metastatic foci in murine brain sections across experimental groups. E Representative bright-field images of brain metastasis-derived organoids from anta-NC and anta-1170 groups. F 3D confocal reconstruction of brain metastasis organoids stained with pan-CK (green, tumor cells) and Ki67 (red, proliferative cells). G Representative images and quantitation of HBMEC tube formation assay using conditioned media from experimental groups. H Schematic of in vitro blood-brain barrier (BBB) transendothelial migration assay. I Representative images (left) and statistical analysis (right) of migrated tumor cells in different groups. Tumor cells were labeled with CMFDA (green) and red arrows point to migrated tumor cells. J Representative images (left) and comparative analysis (right) of TNBC cell migratory capacity between groups. K Representative images (left) and quantitative analyses (right) of the migration area in the scratch wound assay. The error bars represent the SDs of triplicate experiments

Journal: Molecular Cancer

Article Title: piR-1170 drives brain metastasis and immune evasion via WTAP-mediated m6A methylation reprogramming in triple-negative breast cancer

doi: 10.1186/s12943-026-02568-y

Figure Lengend Snippet: piR-1170 confers survival advantage in TNBC brain metastasis. A Schematic of intracranial injection-based brain metastasis model. B-C In vivo bioluminescence imaging ( B ) and corresponding fluorescence intensities ( C ) at 1 day, 3 days, 7 days and 11 days post-implantation ( n = 6 per group). D Representative HE staining images of metastatic foci in murine brain sections across experimental groups. E Representative bright-field images of brain metastasis-derived organoids from anta-NC and anta-1170 groups. F 3D confocal reconstruction of brain metastasis organoids stained with pan-CK (green, tumor cells) and Ki67 (red, proliferative cells). G Representative images and quantitation of HBMEC tube formation assay using conditioned media from experimental groups. H Schematic of in vitro blood-brain barrier (BBB) transendothelial migration assay. I Representative images (left) and statistical analysis (right) of migrated tumor cells in different groups. Tumor cells were labeled with CMFDA (green) and red arrows point to migrated tumor cells. J Representative images (left) and comparative analysis (right) of TNBC cell migratory capacity between groups. K Representative images (left) and quantitative analyses (right) of the migration area in the scratch wound assay. The error bars represent the SDs of triplicate experiments

Article Snippet: Then, the tops of the monolayers were seeded with cancer cells labeled with CellTracker Green CMFDA (Yeasen Biotech, Shanghai, China).

Techniques: Injection, In Vivo, Imaging, Fluorescence, Staining, Derivative Assay, Quantitation Assay, Tube Formation Assay, In Vitro, Migration, Labeling, Scratch Wound Assay Assay