bio rad native buffer Search Results


96
Bio-Rad glycine
Glycine, 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
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92
Bio-Rad buffer kit
Buffer Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
Bio-Rad native polyacrylamide gel
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Native Polyacrylamide Gel, supplied by Bio-Rad, 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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95
Bio-Rad bio rad native buffer
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Bio Rad Native Buffer, supplied by Bio-Rad, 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
bio rad native buffer - by Bioz Stars, 2026-05
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93
Bio-Rad native imac elution buffer
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Native Imac Elution Buffer, supplied by Bio-Rad, 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
native imac elution buffer - by Bioz Stars, 2026-05
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85
Bio-Rad native imac wash buffer
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Native Imac Wash Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Bio-Rad native imac lysis buffer
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Native Imac Lysis Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 91 stars, based on 1 article reviews
native imac lysis buffer - by Bioz Stars, 2026-05
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90
Cosmo Bio USA native page loading buffer
Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% <t>polyacrylamide</t> gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.
Native Page Loading Buffer, supplied by Cosmo Bio USA, 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/native page loading buffer/product/Cosmo Bio USA
Average 90 stars, based on 1 article reviews
native page loading buffer - by Bioz Stars, 2026-05
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Image Search Results


Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% polyacrylamide gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.

Journal: PLoS ONE

Article Title: Physical Analyses of E. coli Heteroduplex Recombination Products In Vivo : On the Prevalence of 5′ and 3′ Patches

doi: 10.1371/journal.pone.0001242

Figure Lengend Snippet: Southern blot of artificial heteroduplexes, made by melting and reannealing the 604 bp long DNA fragment with and without an 18 bp insertion marker, run on a 5% polyacrylamide gel. (A) Hybridization of the blot with a PCR-labeled probe complementary to the entire 604 bp restriction fragment. (B) Hybridization with an oligo probe complementary to the loop sequence in the strand ending 5′ at the right. (C) Hybridization with an oligo probe complementary to the loop sequence in the 3′-ending strand. “+”, the homoduplex fragment containing the 18 bp insert; “-”, the homoduplex fragment with no insert; “mixed”, melted and reannealed “+” and “−” DNAs (artificially prepared heteroduplexes). Figures beneath the gels represent the structures of Homo- and Het-containing fragments, showing the sequences of the complementary loops. “Het”, heteroduplex; “Homo”, homoduplex.

Article Snippet: Either one or two different amounts of DNA for each cross was loaded onto a 5% native polyacrylamide gel (BioRad), and run in 1X TBE buffer (BioRad) at room temperature for approximately 140 minutes at 110V. (Undiluted restriction digests were loaded using Ficoll loading dye, diluted digests were loaded using glycerol loading dye .)

Techniques: Southern Blot, Marker, Hybridization, Labeling, Sequencing