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Celigo Inc celigo s imaging cytometer
Celigo S Imaging Cytometer, supplied by Celigo Inc, 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/celigo+imaging+cytometer/celigo+cytometer+image/pmc08891081-354-5-5
Average 86 stars, based on 1 article reviews
celigo s imaging cytometer - by Bioz Stars, 2026-09
86/100 stars

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Related Articles

Multiple Displacement Amplification:

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux
Article Snippet: .. Death of indicated MDA-MB-468 cell clones treated with indicated concentrations of thapsigargin ( d ), ebastine ( e , left) or terfenadine ( e , right) for 24 h. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca 2+ ] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24 h and analyzed as in ( d ). h Cytosolic [Ca 2+ ] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15 μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 ( a , b ), ≥5000 ( c , f , h ) or ≥15000 ( d , e , i ) cells analyzed in each sample. ..

Clone Assay:

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux
Article Snippet: .. Death of indicated MDA-MB-468 cell clones treated with indicated concentrations of thapsigargin ( d ), ebastine ( e , left) or terfenadine ( e , right) for 24 h. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca 2+ ] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24 h and analyzed as in ( d ). h Cytosolic [Ca 2+ ] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15 μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 ( a , b ), ≥5000 ( c , f , h ) or ≥15000 ( d , e , i ) cells analyzed in each sample. ..

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux.
Article Snippet: Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. .. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. ..

Staining:

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux
Article Snippet: .. Death of indicated MDA-MB-468 cell clones treated with indicated concentrations of thapsigargin ( d ), ebastine ( e , left) or terfenadine ( e , right) for 24 h. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca 2+ ] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24 h and analyzed as in ( d ). h Cytosolic [Ca 2+ ] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15 μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 ( a , b ), ≥5000 ( c , f , h ) or ≥15000 ( d , e , i ) cells analyzed in each sample. ..

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux.
Article Snippet: Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. .. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. ..

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: On the day of the CTG assay, the live cell dye, Calcein AM (Thermo Fisher, cat. No. C3100MP), and the dead cell dye, Ethidium Homodimer-2 (Thermo Fisher, cat. No. E3599), were spiked into each well at the working concentrations of 0.5 μM and 2 μM, respectively. .. After incubation for 45 min at 37 oC, the stained plates were scanned by Celigo Imaging Cytometer. ..

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer. ..

Imaging:

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux
Article Snippet: .. Death of indicated MDA-MB-468 cell clones treated with indicated concentrations of thapsigargin ( d ), ebastine ( e , left) or terfenadine ( e , right) for 24 h. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca 2+ ] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24 h and analyzed as in ( d ). h Cytosolic [Ca 2+ ] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15 μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 ( a , b ), ≥5000 ( c , f , h ) or ≥15000 ( d , e , i ) cells analyzed in each sample. ..

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: .. The training dataset consists of a sample of brightfield images of well-established CRC MOS and paired CAM fluorescence images, all collected by using a Celigo Imaging Cytometer. ..

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux.
Article Snippet: Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. .. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. ..

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The percentage of total foci that existed as microplaques was determined alongside the mean microplaque area as measured by the Celigo. .. The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer.

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: On the day of the CTG assay, the live cell dye, Calcein AM (Thermo Fisher, cat. No. C3100MP), and the dead cell dye, Ethidium Homodimer-2 (Thermo Fisher, cat. No. E3599), were spiked into each well at the working concentrations of 0.5 μM and 2 μM, respectively. .. After incubation for 45 min at 37 oC, the stained plates were scanned by Celigo Imaging Cytometer. ..

Article Title: Gold decorated bismuth sulfide nanorods for enhanced computed tomography imaging with in vitro and in vivo validation.
Article Snippet: .. To further verify in vitro uptake of Au@Bi2S3 NRs in UC-MSCs, FITC-Au@Bi2S3 NRs cellular uptake and intracellular localization of particles within UC-MSCs were assessed using a Celigo Imaging Cytometer in a time-series dynamic study (up to 12 h). ..

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer. ..

Article Title: Therapeutic Induction of Ferroptosis in Tumors Using PD-L1 Targeting Antibody Nanogel Conjugates
Article Snippet: .. The number and ratio of dead/live cells for each treatment were quantified using a Celigo imaging cytometer. .. To quantify total ROS, tumor cells were trypsinized, washed with PBS, and incubated with 2’,7’-dichlorodihydrofluorescein diacetate (H 2 DCFDA) (Invitrogen, D399) at 1 μM for 30 mins at room temperature.

Cytometry:

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux
Article Snippet: .. Death of indicated MDA-MB-468 cell clones treated with indicated concentrations of thapsigargin ( d ), ebastine ( e , left) or terfenadine ( e , right) for 24 h. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca 2+ ] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24 h and analyzed as in ( d ). h Cytosolic [Ca 2+ ] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15 μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 ( a , b ), ≥5000 ( c , f , h ) or ≥15000 ( d , e , i ) cells analyzed in each sample. ..

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: .. The training dataset consists of a sample of brightfield images of well-established CRC MOS and paired CAM fluorescence images, all collected by using a Celigo Imaging Cytometer. ..

Article Title: Lysosomal TMEM165 controls cellular ion homeostasis and survival by mediating lysosomal Ca 2+ import and H + efflux.
Article Snippet: Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. .. Cells were stained with propidium iodide (dead cells) and Hoechst-33342 (total cells) and cell death was analyzed by Celigo Imaging Cytometer. f Cytosolic [Ca2+] in WT and TMEM165-KO HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. g Death of indicated HeLa clones treated with 0–15 μM ebastine for 24h and analyzed as in (d). h Cytosolic [Ca2+] in indicated HeLa clones treated with DMSO or 15 μM ebastine for 1 h and analyzed by Fluo-4-AM. i Death of indicated HeLa cell clones treated with 6 μM terfenadine or 15 μM ebastine for 24 h. Cells were stained with SYTOX Green (dead cells) andHoechst-33342 (total cells) and cell deathwas analyzedbyCeligo Imaging Cytometer. j Galectin 1 puncta (leaky lysosomes) in indicated HeLa clones treated with DMSO or 15μM ebastine for the last 16 h. Bars, SD of three independent experiments with 30 (a, b), ≥5000 (c, f, h) or ≥15000 (d, e, i) cells analyzed in each sample. ..

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The percentage of total foci that existed as microplaques was determined alongside the mean microplaque area as measured by the Celigo. .. The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer.

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: On the day of the CTG assay, the live cell dye, Calcein AM (Thermo Fisher, cat. No. C3100MP), and the dead cell dye, Ethidium Homodimer-2 (Thermo Fisher, cat. No. E3599), were spiked into each well at the working concentrations of 0.5 μM and 2 μM, respectively. .. After incubation for 45 min at 37 oC, the stained plates were scanned by Celigo Imaging Cytometer. ..

Article Title: Gold decorated bismuth sulfide nanorods for enhanced computed tomography imaging with in vitro and in vivo validation.
Article Snippet: .. To further verify in vitro uptake of Au@Bi2S3 NRs in UC-MSCs, FITC-Au@Bi2S3 NRs cellular uptake and intracellular localization of particles within UC-MSCs were assessed using a Celigo Imaging Cytometer in a time-series dynamic study (up to 12 h). ..

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer. ..

Article Title: Therapeutic Induction of Ferroptosis in Tumors Using PD-L1 Targeting Antibody Nanogel Conjugates
Article Snippet: .. The number and ratio of dead/live cells for each treatment were quantified using a Celigo imaging cytometer. .. To quantify total ROS, tumor cells were trypsinized, washed with PBS, and incubated with 2’,7’-dichlorodihydrofluorescein diacetate (H 2 DCFDA) (Invitrogen, D399) at 1 μM for 30 mins at room temperature.

Chick Chorioallantoic Membrane Assay:

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: .. The training dataset consists of a sample of brightfield images of well-established CRC MOS and paired CAM fluorescence images, all collected by using a Celigo Imaging Cytometer. ..

Fluorescence:

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: .. The training dataset consists of a sample of brightfield images of well-established CRC MOS and paired CAM fluorescence images, all collected by using a Celigo Imaging Cytometer. ..

Incubation:

Article Title: Rapid tissue prototyping with micro-organospheres
Article Snippet: On the day of the CTG assay, the live cell dye, Calcein AM (Thermo Fisher, cat. No. C3100MP), and the dead cell dye, Ethidium Homodimer-2 (Thermo Fisher, cat. No. E3599), were spiked into each well at the working concentrations of 0.5 μM and 2 μM, respectively. .. After incubation for 45 min at 37 oC, the stained plates were scanned by Celigo Imaging Cytometer. ..

In Vitro:

Article Title: Gold decorated bismuth sulfide nanorods for enhanced computed tomography imaging with in vitro and in vivo validation.
Article Snippet: .. To further verify in vitro uptake of Au@Bi2S3 NRs in UC-MSCs, FITC-Au@Bi2S3 NRs cellular uptake and intracellular localization of particles within UC-MSCs were assessed using a Celigo Imaging Cytometer in a time-series dynamic study (up to 12 h). ..

Software:

Article Title: Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis.
Article Snippet: The detection of cells positive for active caspase 3/7 and ZsGreen was performed on a Celigo imaging cytometer. .. The Hoechst stain was used to apply a nuclei mask within the analysis software on the Celigo imaging cytometer. ..



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