fluorescent dna binding dye sybrgreen ii Search Results


lightcycler faststart dna master sybr green i kit  (Roche)
99
Roche lightcycler faststart dna master sybr green i kit
Lightcycler Faststart Dna Master Sybr Green I Kit, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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lightcycler faststart dna master sybr green i kit - by Bioz Stars, 2026-03
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fluorescent dna binding dye sybrgreen ii  (Thermo Fisher)
99
Thermo Fisher fluorescent dna binding dye sybrgreen ii
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Fluorescent Dna Binding Dye Sybrgreen Ii, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
fluorescent dna binding dye sybrgreen ii - by Bioz Stars, 2026-03
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fluorescent dna binding dye  (Thermo Fisher)
99
Thermo Fisher fluorescent dna binding dye
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Fluorescent Dna Binding Dye, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fluorescent dna binding dye/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
fluorescent dna binding dye - by Bioz Stars, 2026-03
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absolute qpcr sybrgreen fluorescence mix  (Thermo Fisher)
90
Thermo Fisher absolute qpcr sybrgreen fluorescence mix
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Absolute Qpcr Sybrgreen Fluorescence Mix, 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
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dna engine opticon continuous fluorescence detection system  (MJ Research)
90
MJ Research dna engine opticon continuous fluorescence detection system
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Dna Engine Opticon Continuous Fluorescence Detection System, supplied by MJ Research, 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
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dna engine opticon continuous fluorescence detection system  (M.J Research Inc)
90
M.J Research Inc dna engine opticon continuous fluorescence detection system
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Dna Engine Opticon Continuous Fluorescence Detection System, supplied by M.J Research Inc, 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/dna engine opticon continuous fluorescence detection system/product/M.J Research Inc
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dna engine opticon continuous fluorescence detection system - by Bioz Stars, 2026-03
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fluorescent dye sybrgreen  (Thermo Fisher)
86
Thermo Fisher fluorescent dye sybrgreen
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Fluorescent Dye Sybrgreen, supplied by Thermo Fisher, 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
fluorescent dye sybrgreen - by Bioz Stars, 2026-03
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quantitect sybrgreen pcr kit  (Qiagen)
90
Qiagen quantitect sybrgreen pcr kit
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Quantitect Sybrgreen Pcr Kit, supplied by Qiagen, 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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sybrgreen i  (Promega)
90
Promega sybrgreen i
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Sybrgreen I, supplied by Promega, 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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sybrgreen i - by Bioz Stars, 2026-03
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sybrgreen  (Trevigen)
90
Trevigen sybrgreen
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Sybrgreen, supplied by Trevigen, 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/sybrgreen/product/Trevigen
Average 90 stars, based on 1 article reviews
sybrgreen - by Bioz Stars, 2026-03
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sybrgreen  (Thermo Fisher)
90
Thermo Fisher sybrgreen
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Sybrgreen, 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/result/sybrgreen/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
sybrgreen - by Bioz Stars, 2026-03
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sybrgreen  (Meridian Bioscience)
90
Meridian Bioscience sybrgreen
Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by <t>SybrGreen</t> II®, was detected using the Geliance 600 Imaging System.
Sybrgreen, supplied by Meridian Bioscience, 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/sybrgreen/product/Meridian Bioscience
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Image Search Results


Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by SybrGreen II®, was detected using the Geliance 600 Imaging System.

Journal: Sensors (Basel, Switzerland)

Article Title: Human Thrombin Detection Through a Sandwich Aptamer Microarray: Interaction Analysis in Solution and in Solid Phase

doi: 10.3390/s111009426

Figure Lengend Snippet: Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA1 and thrombin in presence (a) and in absence of Potassium (b) . TBA1 was incubated with the protein under the conditions described. We have indicated in the figure the respective TBA1 and thrombin concentrations. A control reaction without thrombin was performed in all experiments. KCl was added to the polyacrilamide gel and to the running buffer. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by SybrGreen II®, was detected using the Geliance 600 Imaging System.

Article Snippet: Aptamers on the gels were stained with the fluorescent DNA binding dye SybrGreen II ® (Invitrogen) that preferentially binds to single-stranded DNA and emits fluorescence (λ exc = 488 nm; λ em = 522 nm) when in complex with DNA.

Techniques: Electrophoretic Mobility Shift Assay, Incubation, Control, Binding Assay, Staining, Imaging

Electrophoretic Mobility Shift Assay (EMSA) of TBA1-NH 2 with thrombin (a) and of TBA1(12T)NH 2 with thrombin (b) . TBA1-NH 2 and TBA(12T)NH 2 were separately incubated with the protein under the conditions described. We have indicated in the figure the respective aptamer and thrombin concentrations. A control reaction without thrombin was performed in all experiments. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10mM. The mobility of free and complexed aptamers, stained by SybrGreen II®, was detected using the Geliance 600 Imaging System.

Journal: Sensors (Basel, Switzerland)

Article Title: Human Thrombin Detection Through a Sandwich Aptamer Microarray: Interaction Analysis in Solution and in Solid Phase

doi: 10.3390/s111009426

Figure Lengend Snippet: Electrophoretic Mobility Shift Assay (EMSA) of TBA1-NH 2 with thrombin (a) and of TBA1(12T)NH 2 with thrombin (b) . TBA1-NH 2 and TBA(12T)NH 2 were separately incubated with the protein under the conditions described. We have indicated in the figure the respective aptamer and thrombin concentrations. A control reaction without thrombin was performed in all experiments. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10mM. The mobility of free and complexed aptamers, stained by SybrGreen II®, was detected using the Geliance 600 Imaging System.

Article Snippet: Aptamers on the gels were stained with the fluorescent DNA binding dye SybrGreen II ® (Invitrogen) that preferentially binds to single-stranded DNA and emits fluorescence (λ exc = 488 nm; λ em = 522 nm) when in complex with DNA.

Techniques: Electrophoretic Mobility Shift Assay, Incubation, Control, Binding Assay, Staining, Imaging

Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA2 with thrombin (a) and TBA2Cy5 with thrombin (b) . Each aptamer was incubated with the protein under the conditions described. We have indicated in the figure the respective aptamer and thrombin concentrations. A control reaction without thrombin was performed in all experiments. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by SybrGreen II ® (a,b) was detected using the Geliance 600 Imaging System.

Journal: Sensors (Basel, Switzerland)

Article Title: Human Thrombin Detection Through a Sandwich Aptamer Microarray: Interaction Analysis in Solution and in Solid Phase

doi: 10.3390/s111009426

Figure Lengend Snippet: Electrophoretic Mobility Shift Assay (EMSA) of unmodified TBA2 with thrombin (a) and TBA2Cy5 with thrombin (b) . Each aptamer was incubated with the protein under the conditions described. We have indicated in the figure the respective aptamer and thrombin concentrations. A control reaction without thrombin was performed in all experiments. Binding reactions were applied on a 12% non-denaturing PAA gel containing 1X TBE buffer and KCl 10 mM. The mobility of free and complexed aptamers, stained by SybrGreen II ® (a,b) was detected using the Geliance 600 Imaging System.

Article Snippet: Aptamers on the gels were stained with the fluorescent DNA binding dye SybrGreen II ® (Invitrogen) that preferentially binds to single-stranded DNA and emits fluorescence (λ exc = 488 nm; λ em = 522 nm) when in complex with DNA.

Techniques: Electrophoretic Mobility Shift Assay, Incubation, Control, Binding Assay, Staining, Imaging