program version 5.0.6 Search Results


grafit5 software analysis version 5.0.6  (ERITHACUS SOFTWARE LIMITED)
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ERITHACUS SOFTWARE LIMITED grafit5 software analysis version 5.0.6
Grafit5 Software Analysis Version 5.0.6, supplied by ERITHACUS SOFTWARE LIMITED, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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grafit5 software analysis version 5.0.6 - by Bioz Stars, 2026-03
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program in the dnastar software  (DNASTAR)
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DNASTAR program in the dnastar software
Program In The Dnastar Software, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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program in the dnastar software - by Bioz Stars, 2026-03
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megalign software  (DNASTAR)
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DNASTAR megalign software
Megalign Software, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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grafit  (ERITHACUS SOFTWARE LIMITED)
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ERITHACUS SOFTWARE LIMITED grafit
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Grafit, supplied by ERITHACUS SOFTWARE LIMITED, 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/result/grafit/product/ERITHACUS SOFTWARE LIMITED
Average 90 stars, based on 1 article reviews
grafit - by Bioz Stars, 2026-03
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pmod image analysis software version 3.506  (PMOD Technologies)
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PMOD Technologies pmod image analysis software version 3.506
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Pmod Image Analysis Software Version 3.506, supplied by PMOD Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
pmod image analysis software version 3.506 - by Bioz Stars, 2026-03
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version 5.0.6 software  (Bioedit Company)
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Bioedit Company version 5.0.6 software
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Version 5.0.6 Software, supplied by Bioedit Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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version 5.0.6 software - by Bioz Stars, 2026-03
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software version 5.06  (DNASTAR)
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DNASTAR software version 5.06
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Software Version 5.06, supplied by DNASTAR, 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/result/software version 5.06/product/DNASTAR
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primerselect program  (DNASTAR)
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DNASTAR primerselect program
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Primerselect Program, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ii sequence analysis software version 5.06  (DNASTAR)
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DNASTAR ii sequence analysis software version 5.06
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Ii Sequence Analysis Software Version 5.06, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bioedit software version 5.0.6  (Abbott Laboratories)
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Abbott Laboratories bioedit software version 5.0.6
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Bioedit Software Version 5.0.6, supplied by Abbott Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bioedit software version 5.0.6 - by Bioz Stars, 2026-03
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prism version 5  (GraphPad Software Inc)
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GraphPad Software Inc prism version 5
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Prism Version 5, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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megaligntm software  (DNASTAR)
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DNASTAR megaligntm software
DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with <t>GraFit</t> <t>software.</t> ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .
Megaligntm Software, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with GraFit software. ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .

Journal: International Journal of Molecular Sciences

Article Title: Disulfiram/Copper Suppresses Cancer Stem Cell Activity in Differentiated Thyroid Cancer Cells by Inhibiting BMI1 Expression

doi: 10.3390/ijms232113276

Figure Lengend Snippet: DSF/copper inhibits cell proliferation and thyrosphere formation of DTC cells. ( A , B ) K1 ( A ) or WRO ( B ) cells were seeded into 96-well-plates and treated with the indicated concentrations of DSF in presence of 1 μM CuCl 2 for 72 h. The cell proliferation was determined by WST-1 reagent and the absorbance was read at 440 nm wavelength. The curves and IC 50 values were drawn and calculated with GraFit software. ( C , D ) K1 ( C ) or WRO ( D ) cells were seeded into ultralow attachment culture dishes to form primary thyrospheres for 7 days under the treatment of indicated concentrations of DSF in presence of 1 μM CuCl 2 . The formed thyrospheres were pictured and counted on Day 7. *, p < 0.05; **, p < 0.01. Scale bars in ( C , D ) represented as 50 nm. ( E ) The thyrospheres from K1 or WRO cells were dissociated into single-cell suspensions by enzyme-free cell dissociation buffer and treated with 200 nM of DSF in presence of 1 μM CuCl 2 for 24 h. The expression of CD44 was determined by flow cytometry. Data were analyzed by FlowJo software. The dotted arrows indicate the percentage of CD44 high expression cells that with the fluorescence intensity greater than 10 4 .

Article Snippet: The IC 50 values were calculated by GraFit (version 5.0.6, Erithacus Software, West Sussex, UK).

Techniques: Software, Expressing, Flow Cytometry, Fluorescence