tris edta Search Results


atpfree tris edta buffer  (Biothema AB)
91
Biothema AB atpfree tris edta buffer
Atpfree Tris Edta Buffer, supplied by Biothema AB, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/atpfree tris edta buffer/product/Biothema AB
Average 91 stars, based on 1 article reviews
atpfree tris edta buffer - by Bioz Stars, 2026-03
91/100 stars
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tris edta buffer  (Thermo Fisher)
99
Thermo Fisher tris edta buffer
Tris Edta Buffer, 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
tris edta buffer - by Bioz Stars, 2026-03
99/100 stars
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1x biorad 9 hercules ca cat 1610743  (Bio-Rad)
96
Bio-Rad 1x biorad 9 hercules ca cat 1610743
1x Biorad 9 Hercules Ca Cat 1610743, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/1x biorad 9 hercules ca cat 1610743/product/Bio-Rad
Average 96 stars, based on 1 article reviews
1x biorad 9 hercules ca cat 1610743 - by Bioz Stars, 2026-03
96/100 stars
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tris acetate edta tae buffer  (Thermo Fisher)
97
Thermo Fisher tris acetate edta tae buffer
Tris Acetate Edta Tae Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
tris acetate edta tae buffer - by Bioz Stars, 2026-03
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concentrated 5x tris borate edta tbe solution  (Thermo Fisher)
99
Thermo Fisher concentrated 5x tris borate edta tbe solution
Concentrated 5x Tris Borate Edta Tbe Solution, 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/concentrated 5x tris borate edta tbe solution/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
concentrated 5x tris borate edta tbe solution - by Bioz Stars, 2026-03
99/100 stars
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tbe buffer  (TaKaRa)
96
TaKaRa tbe buffer
Tbe Buffer, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
tbe buffer - by Bioz Stars, 2026-03
96/100 stars
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secondary antibody 647 goat anti rabbit thermofisher  (Thermo Fisher)
95
Thermo Fisher secondary antibody 647 goat anti rabbit thermofisher
Secondary Antibody 647 Goat Anti Rabbit Thermofisher, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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tbe  (Bio-Rad)
99
Bio-Rad tbe
( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. <t>The</t> <t>separation</t> was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× <t>TBE.</t> The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.
Tbe, supplied by Bio-Rad, 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/tbe/product/Bio-Rad
Average 99 stars, based on 1 article reviews
tbe - by Bioz Stars, 2026-03
99/100 stars
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te buffer  (Boston BioProducts)
93
Boston BioProducts te buffer
( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. <t>The</t> <t>separation</t> was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× <t>TBE.</t> The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.
Te Buffer, supplied by Boston BioProducts, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
te buffer - by Bioz Stars, 2026-03
93/100 stars
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te 10 mm tris ph 8 0 1 mm edta  (Thermo Fisher)
95
Thermo Fisher te 10 mm tris ph 8 0 1 mm edta
( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. <t>The</t> <t>separation</t> was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× <t>TBE.</t> The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.
Te 10 Mm Tris Ph 8 0 1 Mm Edta, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
te 10 mm tris ph 8 0 1 mm edta - by Bioz Stars, 2026-03
95/100 stars
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t0224  (Teknova)
93
Teknova t0224
( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. <t>The</t> <t>separation</t> was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× <t>TBE.</t> The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.
T0224, supplied by Teknova, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/t0224/product/Teknova
Average 93 stars, based on 1 article reviews
t0224 - by Bioz Stars, 2026-03
93/100 stars
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tris borate edta buffer  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology tris borate edta buffer
Summary of the experimental conditions and antibodies used for IF analysis.
Tris Borate Edta Buffer, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tris borate edta buffer/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
tris borate edta buffer - by Bioz Stars, 2026-03
93/100 stars
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Image Search Results


( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. The separation was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× TBE. The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.

Journal: Nucleic Acids Research

Article Title: Purification and preconcentration of genomic DNA from whole cell lysates using photoactivated polycarbonate (PPC) microfluidic chips

doi: 10.1093/nar/gkl146

Figure Lengend Snippet: ( A ) Fluorescence images of agarose gels showing the presence of the 600 bp amplicon generated from PCR performed on the PPC-purified E.coli gDNA obtained from purifications run on the same chip. After gDNA immobilization, DNA sizing ladder (lane a); the microchip was rinsed with 200 µl of 85% ethanol followed by 20 µl of DI water (lane b); the chip was rinsed with 50 µl of 85% ethanol followed by 20 µl of DI water (lane c); control PCR containing gDNA isolated from E.coli containing 1.7% ethanol (lanes d and e). ( B ) Gel images of the 600 bp amplicons obtained from PCR performed with the PPC-purified E.coli at different aliquot numbers of water (20 µl each) used to elute the DNA from the immobilization bed. Lane a, DNA sizing ladder; lane b, fraction 1 (20 µl); lane c, fraction 2 (20 µl); and lane d, fraction 3 (20 µl). The samples were immobilized in buffer containing 3% PEG, 0.4 M NaCl and 70% ethanol. The separation was performed on a 3% agarose gel using a field strength of 4.8 V/cm in 1× TBE. The sample volume loaded onto the gel was 10 µl, which also contained 2 µl of the loading dye. The gels were stained with SYBR Green I prior to imaging.

Article Snippet: Amplicons were indexed against a DNA sizing ladder (50–1000 bp; Molecular Probes, Eugene, OR) with the separation performed at 4.8 V/cm in 1× TBE (Tris–boric acid/EDTA) (Bio-Rad Laboratories).

Techniques: Fluorescence, Amplification, Generated, Purification, MicroChIP Assay, Control, Isolation, Agarose Gel Electrophoresis, Staining, SYBR Green Assay, Imaging

Summary of the experimental conditions and antibodies used for IF analysis.

Journal: Cancers

Article Title: Picturing Breast Cancer Brain Metastasis Development to Unravel Molecular Players and Cellular Crosstalk

doi: 10.3390/cancers13040910

Figure Lengend Snippet: Summary of the experimental conditions and antibodies used for IF analysis.

Article Snippet: Thrombin , 10 mM Tris-borate EDTA buffer pH 8.0 , - , 3% BSA , Thrombin (1:200) Santa Cruz Biotechnology #sc-271449, Mouse Mc , Alexa Fluor ® 647 (1:500) Thermo Fisher Scientific, #A-21235, Goat anti-Mouse.

Techniques: Blocking Assay, Plasmid Preparation